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Compile Data Set for Download or QSAR

Found 450 hits with Last Name = 'greer' and Initial = 'j'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470113
PNG
(CHEMBL439134)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCCNC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CCCCNC(=O)c1cccnc1)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)CCc1ccc(F)cc1
Show InChI InChI=1S/C69H92FN11O11/c1-7-72-66(89)59-24-16-38-81(59)69(92)55(23-11-12-36-73-45(4)5)77-64(87)56(39-44(2)3)78-63(86)54(22-10-13-37-74-62(85)50-20-15-35-71-42-50)76-67(90)60(40-47-27-32-52(83)33-28-47)80(6)68(91)58(43-82)79-65(88)57(41-49-19-14-18-48-17-8-9-21-53(48)49)75-61(84)34-29-46-25-30-51(70)31-26-46/h8-9,14-15,17-21,25-28,30-33,35,42,44-45,54-60,73,82-83H,7,10-13,16,22-24,29,34,36-41,43H2,1-6H3,(H,72,89)(H,74,85)(H,75,84)(H,76,90)(H,77,87)(H,78,86)(H,79,88)/t54-,55+,56+,57+,58+,59-,60+/m1/s1
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0.00200n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470098
PNG
(CHEMBL2371296)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:55.60,43.54,12.20,wD:31.41,23.28,5.4,61.64,(-4.86,4.47,;-3.76,3.4,;-4.14,1.91,;-3.04,.83,;-1.56,1.25,;-3.42,-.66,;-4.85,-1.23,;-4.76,-2.77,;-3.26,-3.15,;-2.44,-1.85,;-.9,-1.75,;-.22,-.37,;-.05,-3.03,;-.73,-4.41,;-2.27,-4.51,;-2.95,-5.89,;-4.49,-5.99,;-5.17,-7.37,;-6.71,-7.47,;-4.32,-8.65,;1.49,-2.93,;2.34,-4.21,;1.66,-5.59,;3.88,-4.12,;4.56,-2.74,;3.71,-1.45,;2.17,-1.55,;4.39,-.07,;4.73,-5.4,;6.27,-5.3,;6.95,-3.92,;7.12,-6.58,;6.44,-7.96,;4.9,-8.06,;4.05,-6.78,;2.51,-6.88,;1.83,-8.26,;.29,-8.35,;2.68,-9.54,;4.22,-9.44,;8.66,-6.48,;9.51,-7.76,;8.83,-9.14,;11.05,-7.66,;11.73,-6.28,;10.88,-5,;11.56,-3.62,;10.71,-2.34,;9.17,-2.44,;8.32,-1.16,;8.49,-3.82,;9.34,-5.1,;11.9,-8.95,;13.44,-8.85,;14.12,-7.47,;14.29,-10.13,;13.61,-11.51,;12.07,-11.61,;15.83,-10.03,;16.69,-11.31,;16,-12.69,;18.22,-11.21,;19.08,-12.5,;20.61,-12.4,;21.6,-13.58,;23.03,-13.01,;22.93,-11.48,;24,-10.37,;23.59,-8.89,;22.1,-8.51,;21.02,-9.61,;21.44,-11.1,;18.91,-9.83,;18.05,-8.55,;16.51,-8.65,;18.73,-7.17,;17.88,-5.89,;18.56,-4.51,;17.71,-3.23,;18.39,-1.85,;19.93,-1.75,;20.61,-.37,;20.78,-3.03,;20.1,-4.41,)|
Show InChI InChI=1S/C60H77FN12O11/c1-4-64-58(83)51-12-8-28-73(51)59(84)45(11-7-27-65-60(62)63)68-53(78)46(29-35(2)3)69-54(79)47(30-37-15-22-41(75)23-16-37)70-55(80)48(31-38-17-24-42(76)25-18-38)71-57(82)50(34-74)72-56(81)49(32-39-33-66-44-10-6-5-9-43(39)44)67-52(77)26-19-36-13-20-40(61)21-14-36/h5-6,9-10,13-18,20-25,33,35,45-51,66,74-76H,4,7-8,11-12,19,26-32,34H2,1-3H3,(H,64,83)(H,67,77)(H,68,78)(H,69,79)(H,70,80)(H,71,82)(H,72,81)(H4,62,63,65)/t45-,46-,47+,48+,49+,50-,51+/m0/s1
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0.0100n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470117
PNG
(CHEMBL264989)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@@H]1CCCN1C(=O)CCc1ccc(F)cc1 |wU:57.63,12.20,wD:63.66,45.57,31.44,23.28,5.4,(20.41,-5.17,;20.43,-6.7,;19.11,-7.49,;17.76,-6.71,;16.46,-7.49,;17.73,-5.22,;18.94,-4.33,;18.43,-2.88,;16.89,-2.9,;16.47,-4.33,;15.14,-5.09,;15.14,-6.64,;13.8,-4.33,;13.82,-2.78,;15.15,-2.01,;15.18,-.48,;16.51,.28,;16.53,1.83,;17.86,2.58,;15.19,2.6,;12.48,-5.07,;11.15,-4.3,;11.16,-2.75,;9.81,-5.06,;9.79,-6.6,;11.13,-7.39,;12.45,-6.62,;11.09,-8.92,;8.47,-4.29,;7.13,-5.04,;7.13,-6.57,;5.81,-4.26,;5.84,-2.72,;5.36,-1.27,;3.9,-.78,;3.9,.76,;5.36,1.25,;6,2.63,;7.52,2.79,;8.44,1.55,;7.8,.13,;6.26,-.01,;4.49,-5.03,;3.14,-4.25,;3.14,-2.71,;1.8,-5,;1.8,-6.54,;3.13,-7.32,;4.46,-6.55,;5.8,-7.35,;5.78,-8.89,;7.1,-9.64,;4.45,-9.64,;3.1,-8.87,;.48,-4.22,;-.86,-4.97,;-.86,-6.52,;-2.18,-4.2,;-2.16,-2.67,;-.84,-1.91,;-3.51,-4.96,;-4.85,-4.19,;-4.83,-2.65,;-6.15,-4.93,;-6.43,-6.44,;-7.96,-6.64,;-8.62,-5.23,;-7.53,-4.17,;-8.3,-2.65,;-7.24,-1.36,;-9.62,-1.85,;-11.1,-2.72,;-12.62,-1.87,;-14.1,-2.74,;-15.57,-1.9,;-15.57,-.17,;-17.05,.76,;-14.1,.7,;-12.62,-.14,)|
Show InChI InChI=1S/C56H75FN12O10/c1-4-60-53(77)46-13-9-27-69(46)55(79)41(12-7-25-61-56(58)59)63-49(73)42(28-33(2)3)64-51(75)44(30-36-31-62-40-11-6-5-10-39(36)40)66-50(74)43(29-35-17-22-38(71)23-18-35)65-52(76)45(32-70)67-54(78)47-14-8-26-68(47)48(72)24-19-34-15-20-37(57)21-16-34/h5-6,10-11,15-18,20-23,31,33,41-47,62,70-71H,4,7-9,12-14,19,24-30,32H2,1-3H3,(H,60,77)(H,63,73)(H,64,75)(H,65,76)(H,66,74)(H,67,78)(H4,58,59,61)/t41-,42-,43-,44+,45-,46+,47-/m0/s1
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0.0120n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470118
PNG
(CHEMBL412751)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H](CCCCNC(=O)c1cccnc1)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)CCc1ccc(F)cc1)C(=O)N[C@@H](CCCCNC(C)C)C(=O)N1CCC[C@@H]1C(N)=O
Show InChI InChI=1S/C67H88FN11O11/c1-42(2)37-54(63(86)75-53(21-9-10-34-71-43(3)4)67(90)79-36-14-22-57(79)60(69)83)76-62(85)52(20-8-11-35-72-61(84)48-18-13-33-70-40-48)74-65(88)58(38-45-25-30-50(81)31-26-45)78(5)66(89)56(41-80)77-64(87)55(39-47-17-12-16-46-15-6-7-19-51(46)47)73-59(82)32-27-44-23-28-49(68)29-24-44/h6-7,12-13,15-19,23-26,28-31,33,40,42-43,52-58,71,80-81H,8-11,14,20-22,27,32,34-39,41H2,1-5H3,(H2,69,83)(H,72,84)(H,73,82)(H,74,88)(H,75,86)(H,76,85)(H,77,87)/t52-,53+,54+,55+,56+,57-,58+/m1/s1
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0.0160n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470080
PNG
(CHEMBL266475)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CCCCNC(=O)c1cccnc1)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:61.66,12.20,wD:23.28,31.46,5.4,67.70,48.50,(24.58,-7.94,;24.59,-9.48,;23.27,-10.25,;21.92,-9.5,;20.64,-10.25,;21.89,-8,;23.11,-7.1,;22.6,-5.68,;21.08,-5.68,;20.64,-7.12,;19.32,-7.87,;19.31,-9.4,;18,-7.1,;18.01,-5.56,;19.35,-4.81,;19.36,-3.28,;20.69,-2.51,;20.7,-.99,;22.02,-.24,;19.38,-.2,;16.66,-7.86,;15.35,-7.09,;15.35,-5.55,;14,-7.84,;14,-9.37,;15.31,-10.15,;16.65,-9.38,;15.3,-11.69,;12.68,-7.07,;11.36,-7.81,;11.34,-9.35,;10.04,-7.04,;10.12,-5.53,;8.92,-4.56,;9.41,-3.11,;8.08,-2.09,;8.74,-.71,;7.87,.6,;8.54,1.98,;6.32,.45,;5.46,1.73,;3.91,1.59,;3.25,.25,;4.15,-1.04,;5.66,-.91,;8.71,-7.81,;7.38,-7.03,;7.38,-5.5,;6.04,-7.77,;6.03,-9.31,;7.35,-10.08,;7.35,-11.62,;8.67,-12.39,;10.01,-11.66,;11.33,-12.42,;10.02,-10.12,;8.69,-9.34,;4.73,-7,;4.73,-5.46,;3.4,-7.74,;3.38,-9.3,;2.06,-6.97,;2.09,-5.46,;3.41,-4.69,;.74,-7.74,;-.6,-6.97,;-.57,-5.43,;-1.92,-7.71,;-1.95,-9.25,;-.61,-10.04,;.8,-9.41,;1.81,-10.57,;1.04,-11.88,;1.49,-13.36,;.46,-14.48,;-1.03,-14.16,;-1.5,-12.68,;-.47,-11.56,;-3.24,-6.96,;-4.58,-7.71,;-4.59,-9.22,;-5.92,-6.96,;-7.37,-7.87,;-8.88,-7.07,;-10.32,-7.99,;-11.84,-7.2,;-11.92,-5.46,;-13.4,-4.6,;-10.48,-4.57,;-8.95,-5.36,)|
Show InChI InChI=1S/C64H85FN14O11/c1-5-69-60(87)53-18-12-32-79(53)63(90)49(17-11-31-71-64(66)67)75-58(85)50(33-39(2)3)76-57(84)48(16-8-9-30-70-56(83)42-13-10-29-68-36-42)74-61(88)54(34-41-21-26-45(81)27-22-41)78(4)62(89)52(38-80)77-59(86)51(35-43-37-72-47-15-7-6-14-46(43)47)73-55(82)28-23-40-19-24-44(65)25-20-40/h6-7,10,13-15,19-22,24-27,29,36-37,39,48-54,72,80-81H,5,8-9,11-12,16-18,23,28,30-35,38H2,1-4H3,(H,69,87)(H,70,83)(H,73,82)(H,74,88)(H,75,85)(H,76,84)(H,77,86)(H4,66,67,71)/t48-,49+,50+,51+,52+,53-,54+/m1/s1
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0.0170n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470097
PNG
(CHEMBL262235)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.80,(30.87,-6.95,;30.88,-8.47,;29.57,-9.26,;28.22,-8.5,;26.93,-9.26,;28.18,-6.99,;29.41,-6.11,;28.89,-4.67,;27.37,-4.67,;26.93,-6.12,;25.61,-6.86,;25.6,-8.4,;24.28,-6.11,;24.29,-4.57,;25.63,-3.81,;25.64,-2.26,;26.98,-1.51,;26.99,.02,;28.31,.79,;25.66,.8,;22.94,-6.86,;21.62,-6.09,;21.62,-4.55,;20.27,-6.83,;20.27,-8.37,;21.59,-9.17,;21.58,-10.69,;22.93,-8.39,;18.95,-6.06,;17.62,-6.82,;17.6,-8.34,;16.31,-6.05,;16.32,-4.51,;15.83,-3.06,;14.39,-2.57,;14.39,-1.03,;15.85,-.56,;16.48,.84,;18.01,1,;18.91,-.24,;18.28,-1.65,;16.73,-1.81,;14.97,-6.8,;13.64,-6.02,;13.64,-4.48,;12.3,-6.79,;12.29,-8.31,;13.6,-9.1,;13.6,-10.62,;14.93,-11.42,;16.27,-10.66,;17.59,-11.43,;16.28,-9.11,;14.95,-8.34,;10.98,-5.99,;9.65,-6.75,;9.63,-8.31,;8.31,-5.98,;8.33,-4.45,;9.66,-3.7,;6.98,-6.73,;5.64,-5.96,;5.67,-4.44,;4.31,-6.72,;4.31,-8.27,;5.63,-9.07,;6.99,-8.33,;8.31,-9.11,;8.24,-10.66,;6.91,-11.4,;6.89,-12.94,;5.54,-13.68,;4.22,-12.9,;4.25,-11.35,;5.6,-10.61,;2.99,-5.96,;1.64,-6.7,;1.72,-8.21,;.26,-6.02,;-1.15,-7.02,;-2.7,-6.31,;-2.88,-4.61,;-4.43,-3.9,;-5.84,-4.9,;-7.36,-4.12,;-5.65,-6.6,;-4.11,-7.31,)|
Show InChI InChI=1S/C64H79FN12O10/c1-4-68-62(86)55-19-11-31-77(55)63(87)49(18-10-30-69-64(66)67)72-57(81)50(32-38(2)3)73-60(84)53(35-43-36-70-48-17-8-7-16-47(43)48)75-58(82)51(33-40-22-27-45(79)28-23-40)74-61(85)54(37-78)76-59(83)52(34-42-14-9-13-41-12-5-6-15-46(41)42)71-56(80)29-24-39-20-25-44(65)26-21-39/h5-9,12-17,20-23,25-28,36,38,49-55,70,78-79H,4,10-11,18-19,24,29-35,37H2,1-3H3,(H,68,86)(H,71,80)(H,72,81)(H,73,84)(H,74,85)(H,75,82)(H,76,83)(H4,66,67,69)/t49-,50-,51-,52-,53+,54-,55+/m0/s1
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0.0170n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470082
PNG
(CHEMBL408861)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)C(Cc1cccc2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,(25.92,-4.76,;25.93,-6.28,;24.61,-7.08,;23.26,-6.31,;21.98,-7.08,;23.23,-4.8,;24.45,-3.92,;23.94,-2.49,;22.42,-2.49,;21.98,-3.93,;20.66,-4.67,;20.65,-6.22,;19.33,-3.92,;19.34,-2.38,;20.68,-1.62,;20.69,-.08,;22.03,.68,;22.04,2.21,;23.36,2.98,;20.71,2.99,;17.99,-4.67,;16.67,-3.9,;16.67,-2.36,;15.32,-4.64,;15.32,-6.19,;16.64,-6.98,;16.63,-8.5,;17.98,-6.21,;14,-3.87,;12.67,-4.63,;12.65,-6.15,;11.35,-3.86,;11.36,-2.33,;10.88,-.87,;9.43,-.39,;9.43,1.16,;10.9,1.63,;11.52,3.02,;13.06,3.18,;13.96,1.95,;13.33,.54,;11.78,.38,;10.01,-4.61,;8.68,-3.84,;8.68,-2.29,;7.34,-4.6,;7.34,-6.12,;8.66,-6.91,;8.65,-8.46,;9.98,-9.23,;11.32,-8.47,;12.64,-9.24,;11.33,-6.93,;10,-6.15,;6.02,-3.81,;4.7,-4.57,;4.67,-6.12,;3.36,-3.79,;3.38,-2.26,;4.71,-1.51,;2.03,-4.55,;.69,-3.77,;.72,-2.25,;-.64,-4.53,;-.64,-6.08,;.68,-6.88,;2.04,-6.14,;3.36,-6.93,;3.29,-8.47,;1.96,-9.21,;1.94,-10.75,;.59,-11.49,;-.73,-10.71,;-.71,-9.17,;.64,-8.43,;-1.96,-3.77,;-3.3,-4.51,;-3.28,-6.05,;-4.65,-3.77,;-6.1,-4.73,;-7.62,-3.96,;-7.72,-2.23,;-9.25,-1.46,;-10.7,-2.39,;-12.19,-1.55,;-10.58,-4.13,;-9.06,-4.9,)|
Show InChI InChI=1S/C64H79FN12O10/c1-4-68-62(86)55-19-11-31-77(55)63(87)49(18-10-30-69-64(66)67)72-57(81)50(32-38(2)3)73-60(84)53(35-43-36-70-48-17-8-7-16-47(43)48)75-58(82)51(33-40-22-27-45(79)28-23-40)74-61(85)54(37-78)76-59(83)52(34-42-14-9-13-41-12-5-6-15-46(41)42)71-56(80)29-24-39-20-25-44(65)26-21-39/h5-9,12-17,20-23,25-28,36,38,49-55,70,78-79H,4,10-11,18-19,24,29-35,37H2,1-3H3,(H,68,86)(H,71,80)(H,72,81)(H,73,84)(H,74,85)(H,75,82)(H,76,83)(H4,66,67,69)/t49-,50-,51-,52?,53+,54-,55+/m0/s1
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0.0170n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470099
PNG
(CHEMBL2371295)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccc(Cl)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:55.60,12.20,wD:43.54,31.41,23.28,5.4,61.64,(27.36,-6,;27.38,-7.53,;26.06,-8.31,;24.72,-7.54,;23.42,-8.31,;24.69,-6.05,;25.9,-5.16,;25.38,-3.71,;23.85,-3.73,;23.43,-5.16,;22.1,-5.92,;22.08,-7.44,;20.76,-5.16,;20.78,-3.61,;22.11,-2.84,;22.14,-1.32,;23.47,-.56,;23.49,.99,;24.82,1.74,;22.15,1.76,;19.44,-5.9,;18.11,-5.13,;18.12,-3.58,;16.77,-5.89,;16.76,-7.43,;18.09,-8.22,;19.41,-7.44,;18.06,-9.75,;15.44,-5.12,;14.1,-5.87,;14.1,-7.4,;12.78,-5.09,;12.88,-3.57,;13.64,-2.23,;12.85,-.9,;13.59,.45,;15.15,.47,;15.9,1.82,;15.94,-.87,;15.19,-2.2,;11.46,-5.86,;10.11,-5.06,;10.11,-3.54,;8.78,-5.83,;8.78,-7.37,;10.1,-8.15,;10.08,-9.7,;11.42,-10.47,;12.75,-9.72,;14.07,-10.47,;12.77,-8.17,;11.43,-7.38,;7.46,-5.05,;6.12,-5.8,;6.11,-7.35,;4.8,-5.03,;4.8,-3.51,;6.12,-2.75,;3.45,-5.79,;2.13,-5.02,;2.16,-3.49,;.78,-5.77,;.78,-7.31,;2.1,-8.09,;3.52,-7.47,;4.55,-8.62,;3.76,-9.95,;4.23,-11.42,;3.2,-12.55,;1.68,-12.23,;1.22,-10.76,;2.26,-9.63,;-.54,-5,;-1.87,-5.76,;-1.79,-7.27,;-3.25,-5.08,;-4.65,-6.09,;-6.21,-5.38,;-7.61,-6.4,;-9.17,-5.71,;-9.35,-4,;-10.9,-3.22,;-7.97,-2.97,;-6.39,-3.68,)|
Show InChI InChI=1S/C60H76ClFN12O10/c1-4-65-58(83)51-12-8-28-74(51)59(84)45(11-7-27-66-60(63)64)69-53(78)46(29-35(2)3)70-54(79)47(30-37-13-20-40(61)21-14-37)71-55(80)48(31-38-17-24-42(76)25-18-38)72-57(82)50(34-75)73-56(81)49(32-39-33-67-44-10-6-5-9-43(39)44)68-52(77)26-19-36-15-22-41(62)23-16-36/h5-6,9-10,13-18,20-25,33,35,45-51,67,75-76H,4,7-8,11-12,19,26-32,34H2,1-3H3,(H,65,83)(H,68,77)(H,69,78)(H,70,79)(H,71,80)(H,72,82)(H,73,81)(H4,63,64,66)/t45-,46-,47+,48-,49-,50-,51+/m0/s1
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0.0180n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470086
PNG
(CHEMBL2369140)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)CCc1ccc(Cl)cc1 |wU:57.63,12.20,63.76,wD:45.57,31.44,23.28,5.4,(27.37,-7.76,;27.37,-9.28,;26.05,-10.07,;24.72,-9.31,;23.41,-10.07,;24.68,-7.8,;25.89,-6.92,;25.37,-5.48,;23.86,-5.48,;23.43,-6.93,;22.09,-7.67,;22.09,-9.22,;20.77,-6.92,;20.77,-5.37,;22.12,-4.61,;22.12,-3.07,;23.47,-2.32,;23.47,-.78,;24.81,-.01,;22.15,,;19.44,-7.67,;18.1,-6.9,;18.12,-5.35,;16.77,-7.64,;16.75,-9.18,;18.09,-9.98,;18.07,-11.5,;19.42,-9.2,;15.43,-6.87,;14.11,-7.63,;14.1,-9.15,;12.79,-6.86,;12.79,-5.32,;12.33,-3.86,;10.86,-3.38,;10.86,-1.83,;12.34,-1.36,;12.95,.03,;14.49,.19,;15.39,-1.04,;14.75,-2.46,;13.23,-2.62,;11.46,-7.61,;10.12,-6.83,;10.12,-5.29,;8.76,-7.6,;8.76,-9.12,;10.08,-9.91,;11.44,-9.15,;12.76,-9.92,;12.76,-11.47,;14.08,-12.24,;11.4,-12.23,;10.08,-11.44,;7.45,-6.8,;6.13,-7.56,;6.09,-9.12,;4.8,-6.79,;4.81,-5.26,;6.13,-4.51,;3.45,-7.54,;2.12,-6.77,;2.13,-5.25,;.78,-7.53,;.78,-9.08,;2.1,-9.88,;3.45,-9.14,;4.77,-9.92,;4.73,-11.47,;6.06,-12.27,;3.38,-12.21,;2.07,-11.43,;-.54,-6.77,;-1.89,-7.51,;-1.82,-9.04,;-3.25,-6.82,;-4.67,-7.8,;-6.23,-7.06,;-7.63,-8.05,;-9.17,-7.32,;-9.33,-5.6,;-10.87,-4.8,;-7.92,-4.61,;-6.36,-5.35,)|
Show InChI InChI=1S/C60H77ClN12O11/c1-4-64-58(83)51-12-8-28-73(51)59(84)45(11-7-27-65-60(62)63)68-53(78)46(29-35(2)3)69-56(81)49(32-39-33-66-44-10-6-5-9-43(39)44)71-55(80)48(31-38-17-24-42(76)25-18-38)70-57(82)50(34-74)72-54(79)47(30-37-15-22-41(75)23-16-37)67-52(77)26-19-36-13-20-40(61)21-14-36/h5-6,9-10,13-18,20-25,33,35,45-51,66,74-76H,4,7-8,11-12,19,26-32,34H2,1-3H3,(H,64,83)(H,67,77)(H,68,78)(H,69,81)(H,70,82)(H,71,80)(H,72,79)(H4,62,63,65)/t45-,46-,47+,48-,49+,50-,51+/m0/s1
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0.0180n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Lutropin-choriogonadotropic hormone receptor


(Rattus norvegicus)
BDBM50405789
PNG
(CHEMBL412984)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H](CCCNC(N)=N)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](Cc1ccc(Cl)cc1)NC(=O)[C@@H](Cc1ccc(Cl)cc1)NC(C)=O)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](C)C(N)=O
Show InChI InChI=1S/C69H92Cl2N18O13/c1-37(2)30-51(60(95)83-50(13-8-28-78-69(75)76)67(102)89-29-9-14-57(89)66(101)80-38(3)58(72)93)84-59(94)49(12-7-27-77-68(73)74)82-62(97)53(33-42-19-25-46(92)26-20-42)86-65(100)56(36-90)88-64(99)55(34-43-35-79-48-11-6-5-10-47(43)48)87-63(98)54(32-41-17-23-45(71)24-18-41)85-61(96)52(81-39(4)91)31-40-15-21-44(70)22-16-40/h5-6,10-11,15-26,35,37-38,49-57,79,90,92H,7-9,12-14,27-34,36H2,1-4H3,(H2,72,93)(H,80,101)(H,81,91)(H,82,97)(H,83,95)(H,84,94)(H,85,96)(H,86,100)(H,87,98)(H,88,99)(H4,73,74,77)(H4,75,76,78)/t38-,49-,50-,51+,52-,53+,54-,55-,56+,57-/m1/s1
PDB

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PubMed
0.0182n/an/an/an/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vitro binding affinity for Luteinizing hormone releasing hormone receptor from rat pituitary cells, expressed as negative logarithm of the equilib...


J Med Chem 32: 2340-4 (1989)


BindingDB Entry DOI: 10.7270/Q2H70H1B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470085
PNG
(CHEMBL438195)
Show SMILES CC(C)C[C@H](NC(=O)[C@@H](CCCCNC(=O)c1cccnc1)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)CCc1ccc(F)cc1)C(=O)N[C@@H](CCCCNC(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](C)C(N)=O
Show InChI InChI=1S/C70H93FN12O12/c1-43(2)38-56(65(90)79-55(22-10-11-35-74-44(3)4)70(95)83-37-15-23-59(83)67(92)76-45(5)62(72)87)80-64(89)54(21-9-12-36-75-63(88)50-19-14-34-73-41-50)78-68(93)60(39-47-26-31-52(85)32-27-47)82(6)69(94)58(42-84)81-66(91)57(40-49-18-13-17-48-16-7-8-20-53(48)49)77-61(86)33-28-46-24-29-51(71)30-25-46/h7-8,13-14,16-20,24-27,29-32,34,41,43-45,54-60,74,84-85H,9-12,15,21-23,28,33,35-40,42H2,1-6H3,(H2,72,87)(H,75,88)(H,76,92)(H,77,86)(H,78,93)(H,79,90)(H,80,89)(H,81,91)/t45-,54-,55+,56+,57+,58+,59-,60+/m1/s1
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0.0200n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470083
PNG
(CHEMBL267709)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CCCCNC(=O)c1cccnc1)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1F |wU:61.66,12.20,wD:23.28,31.46,5.4,67.70,48.50,(22.09,-4.06,;22.09,-5.58,;20.77,-6.37,;19.44,-5.61,;18.13,-6.37,;19.41,-4.1,;20.61,-3.22,;20.09,-1.78,;18.58,-1.78,;18.15,-3.23,;16.81,-3.97,;16.81,-5.51,;15.49,-3.22,;15.49,-1.67,;16.84,-.91,;16.84,.63,;18.2,1.38,;18.2,2.92,;19.54,3.69,;16.88,3.7,;14.16,-3.97,;12.82,-3.2,;12.84,-1.65,;11.49,-3.94,;11.47,-5.48,;12.81,-6.28,;14.14,-5.5,;12.79,-7.8,;10.15,-3.17,;8.83,-3.93,;8.82,-5.45,;7.51,-3.15,;7.6,-1.62,;6.38,-.65,;6.89,.79,;5.55,1.82,;6.19,3.21,;5.32,4.51,;6,5.89,;3.78,4.37,;2.94,5.65,;1.36,5.53,;.71,4.15,;1.59,2.86,;3.12,2.99,;6.18,-3.91,;4.84,-3.13,;4.84,-1.59,;3.49,-3.89,;3.49,-5.42,;4.81,-6.21,;4.81,-7.76,;6.13,-8.53,;7.48,-7.77,;8.8,-8.54,;7.48,-6.22,;6.16,-5.45,;2.17,-3.1,;2.19,-1.56,;.85,-3.86,;.82,-5.42,;-.48,-3.09,;-.47,-1.56,;.85,-.8,;-1.82,-3.84,;-3.15,-3.07,;-3.14,-1.54,;-4.5,-3.83,;-4.51,-5.38,;-3.18,-6.16,;-1.76,-5.54,;-.74,-6.67,;-1.53,-8.01,;-1.06,-9.47,;-2.09,-10.6,;-3.59,-10.28,;-4.08,-8.82,;-3.03,-7.69,;-5.81,-3.07,;-7.17,-3.81,;-7.13,-5.34,;-8.52,-3.1,;-9.95,-4.06,;-11.51,-3.29,;-11.61,-1.58,;-13.15,-.82,;-14.58,-1.78,;-16.07,-.94,;-14.45,-3.51,;-12.93,-4.26,;-12.9,-5.99,)|
Show InChI InChI=1S/C64H84F2N14O11/c1-5-70-60(88)53-18-12-30-80(53)63(91)49(17-11-29-72-64(67)68)76-58(86)50(31-38(2)3)77-57(85)48(16-8-9-28-71-56(84)41-13-10-27-69-35-41)75-61(89)54(32-39-19-24-44(82)25-20-39)79(4)62(90)52(37-81)78-59(87)51(33-42-36-73-47-15-7-6-14-45(42)47)74-55(83)26-22-40-21-23-43(65)34-46(40)66/h6-7,10,13-15,19-21,23-25,27,34-36,38,48-54,73,81-82H,5,8-9,11-12,16-18,22,26,28-33,37H2,1-4H3,(H,70,88)(H,71,84)(H,74,83)(H,75,89)(H,76,86)(H,77,85)(H,78,87)(H4,67,68,72)/t48-,49+,50+,51+,52+,53-,54+/m1/s1
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0.0200n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470084
PNG
(CHEMBL428299)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CCCCNC(=O)c1cccnc1)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(Cl)cc1 |wU:61.66,12.20,wD:23.28,31.46,5.4,67.70,48.50,(21.23,-6.64,;21.25,-8.17,;19.93,-8.96,;18.58,-8.2,;17.28,-8.96,;18.55,-6.69,;19.77,-5.8,;19.25,-4.36,;17.71,-4.36,;17.29,-5.81,;15.96,-6.56,;15.94,-8.1,;14.62,-5.8,;14.64,-4.26,;15.97,-3.49,;15.99,-1.95,;17.33,-1.19,;17.35,.34,;18.68,1.12,;16,1.13,;13.3,-6.56,;11.96,-5.78,;11.97,-4.23,;10.62,-6.52,;10.61,-8.07,;11.94,-8.87,;13.26,-8.09,;11.91,-10.39,;9.29,-5.75,;7.94,-6.51,;7.94,-8.04,;6.62,-5.74,;6.72,-4.2,;5.49,-3.24,;6.01,-1.78,;4.65,-.75,;5.32,.63,;4.46,1.93,;5.13,3.32,;2.88,1.79,;2.04,3.08,;.46,2.96,;-.18,1.58,;.71,.29,;2.24,.42,;5.29,-6.49,;3.94,-5.72,;3.94,-4.17,;2.61,-6.48,;2.59,-8.01,;3.91,-8.8,;3.91,-10.33,;5.26,-11.12,;6.59,-10.36,;7.91,-11.14,;6.61,-8.81,;5.27,-8.04,;1.29,-5.69,;1.3,-4.14,;-.05,-6.45,;-.06,-8.01,;-1.38,-5.68,;-1.38,-4.14,;-.03,-3.39,;-2.73,-6.43,;-4.05,-5.65,;-4.03,-4.13,;-5.41,-6.42,;-5.41,-7.96,;-4.08,-8.75,;-2.67,-8.13,;-1.63,-9.27,;-2.42,-10.61,;-1.96,-12.07,;-2.99,-13.2,;-4.5,-12.88,;-4.97,-11.41,;-3.92,-10.29,;-6.73,-5.65,;-8.05,-6.42,;-8.08,-7.93,;-9.38,-5.62,;-10.86,-6.52,;-12.37,-5.69,;-13.83,-6.59,;-15.34,-5.77,;-15.4,-4.04,;-17.04,-3.56,;-13.92,-3.14,;-12.4,-3.98,)|
Show InChI InChI=1S/C64H85ClN14O11/c1-5-69-60(87)53-18-12-32-79(53)63(90)49(17-11-31-71-64(66)67)75-58(85)50(33-39(2)3)76-57(84)48(16-8-9-30-70-56(83)42-13-10-29-68-36-42)74-61(88)54(34-41-21-26-45(81)27-22-41)78(4)62(89)52(38-80)77-59(86)51(35-43-37-72-47-15-7-6-14-46(43)47)73-55(82)28-23-40-19-24-44(65)25-20-40/h6-7,10,13-15,19-22,24-27,29,36-37,39,48-54,72,80-81H,5,8-9,11-12,16-18,23,28,30-35,38H2,1-4H3,(H,69,87)(H,70,83)(H,73,82)(H,74,88)(H,75,85)(H,76,84)(H,77,86)(H4,66,67,71)/t48-,49+,50+,51+,52+,53-,54+/m1/s1
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UniChem
Article
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0.0200n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470106
PNG
(CHEMBL413660)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)CCc1ccc(F)cc1 |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.76,(28.79,-5.89,;28.8,-7.42,;27.48,-8.2,;26.14,-7.43,;24.85,-8.2,;26.1,-5.94,;27.32,-5.06,;26.81,-3.61,;25.29,-3.63,;24.85,-5.06,;23.53,-5.82,;23.52,-7.34,;22.2,-5.06,;22.21,-3.51,;23.55,-2.74,;23.56,-1.22,;24.9,-.46,;24.91,1.08,;26.23,1.83,;23.59,1.85,;20.87,-5.79,;19.55,-5.02,;19.55,-3.48,;18.2,-5.78,;18.2,-7.33,;19.52,-8.11,;19.5,-9.64,;20.85,-7.34,;16.88,-5.01,;15.55,-5.76,;15.53,-7.29,;14.24,-4.99,;14.25,-3.45,;13.76,-2,;12.32,-1.52,;12.32,.02,;13.79,.5,;14.41,1.89,;15.94,2.05,;16.84,.8,;16.21,-.61,;14.66,-.75,;12.9,-5.75,;11.57,-4.96,;11.57,-3.44,;10.23,-5.73,;10.23,-7.26,;11.55,-8.04,;12.89,-7.27,;14.21,-8.07,;14.2,-9.61,;15.52,-10.36,;12.86,-10.36,;11.54,-9.59,;8.91,-4.95,;7.58,-5.7,;7.56,-7.24,;6.24,-4.93,;6.27,-3.41,;7.59,-2.65,;4.92,-5.69,;3.58,-4.92,;3.61,-3.38,;2.25,-5.67,;2.25,-7.21,;3.57,-8.01,;4.93,-7.27,;6.24,-8.07,;6.18,-9.61,;7.52,-10.41,;4.83,-10.35,;3.53,-9.55,;.93,-4.9,;-.41,-5.63,;-.41,-7.17,;-1.76,-4.9,;-3.2,-5.83,;-4.74,-5.04,;-6.16,-5.98,;-7.7,-5.18,;-7.78,-3.47,;-9.28,-2.61,;-6.33,-2.54,;-4.81,-3.32,)|
Show InChI InChI=1S/C60H77FN12O11/c1-4-64-58(83)51-12-8-28-73(51)59(84)45(11-7-27-65-60(62)63)68-53(78)46(29-35(2)3)69-56(81)49(32-39-33-66-44-10-6-5-9-43(39)44)71-55(80)48(31-38-17-24-42(76)25-18-38)70-57(82)50(34-74)72-54(79)47(30-37-15-22-41(75)23-16-37)67-52(77)26-19-36-13-20-40(61)21-14-36/h5-6,9-10,13-18,20-25,33,35,45-51,66,74-76H,4,7-8,11-12,19,26-32,34H2,1-3H3,(H,64,83)(H,67,77)(H,68,78)(H,69,81)(H,70,82)(H,71,80)(H,72,79)(H4,62,63,65)/t45-,46-,47-,48-,49+,50-,51+/m0/s1
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Article
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0.0220n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470105
PNG
(CHEMBL405993)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CCCCNC(=O)c1cccnc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:60.65,12.20,wD:48.59,23.28,31.46,5.4,66.69,(29.35,-7.64,;29.38,-9.17,;28.05,-9.96,;26.71,-9.2,;25.41,-9.96,;26.68,-7.69,;27.89,-6.8,;27.38,-5.36,;25.84,-5.36,;25.42,-6.81,;24.09,-7.56,;24.07,-9.1,;22.74,-6.8,;22.77,-5.26,;24.1,-4.49,;24.12,-2.95,;25.45,-2.19,;25.47,-.66,;26.81,.12,;24.13,.13,;21.42,-7.56,;20.09,-6.78,;20.1,-5.23,;18.75,-7.52,;18.73,-9.07,;20.07,-9.87,;20.04,-11.39,;21.39,-9.09,;17.41,-6.75,;16.07,-7.51,;16.07,-9.04,;14.75,-6.74,;14.84,-5.2,;13.62,-4.24,;14.13,-2.78,;12.78,-1.75,;13.45,-.37,;12.59,.94,;13.25,2.32,;11.01,.8,;10.17,2.09,;8.59,1.96,;7.94,.58,;8.84,-.71,;10.36,-.56,;13.43,-7.49,;12.07,-6.72,;12.07,-5.17,;10.74,-7.48,;10.74,-9.01,;12.06,-9.8,;13.39,-9.04,;14.74,-9.81,;14.71,-11.36,;16.04,-12.14,;13.38,-12.12,;12.04,-11.35,;9.42,-6.69,;8.07,-7.45,;8.06,-9.01,;6.75,-6.67,;6.75,-5.14,;8.09,-4.39,;5.4,-7.43,;4.07,-6.65,;4.1,-5.13,;2.72,-7.42,;2.72,-8.96,;4.04,-9.75,;5.46,-9.13,;6.49,-10.26,;5.71,-11.61,;6.17,-13.07,;5.14,-14.2,;3.62,-13.88,;3.16,-12.41,;4.2,-11.29,;1.4,-6.65,;.06,-7.4,;.06,-8.93,;-1.28,-6.65,;-2.74,-7.58,;-4.28,-6.78,;-4.34,-5.06,;-5.87,-4.27,;-7.32,-5.19,;-8.82,-4.32,;-7.24,-6.91,;-5.71,-7.71,)|
Show InChI InChI=1S/C63H83FN14O11/c1-4-68-61(88)53-17-11-31-78(53)62(89)48(16-10-30-70-63(65)66)74-57(84)49(32-38(2)3)75-56(83)47(15-7-8-29-69-55(82)41-12-9-28-67-35-41)73-58(85)50(33-40-20-25-44(80)26-21-40)76-60(87)52(37-79)77-59(86)51(34-42-36-71-46-14-6-5-13-45(42)46)72-54(81)27-22-39-18-23-43(64)24-19-39/h5-6,9,12-14,18-21,23-26,28,35-36,38,47-53,71,79-80H,4,7-8,10-11,15-17,22,27,29-34,37H2,1-3H3,(H,68,88)(H,69,82)(H,72,81)(H,73,85)(H,74,84)(H,75,83)(H,76,87)(H,77,86)(H4,65,66,70)/t47-,48+,49+,50+,51+,52+,53-/m1/s1
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Article
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0.0230n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470132
PNG
(CHEMBL2370208)
Show SMILES CCNC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCC(=O)N1 |wU:88.94,63.67,31.32,45.48,23.24,wD:5.4,77.83,57.61,12.13,(36.44,8.14,;34.94,7.83,;34.46,6.38,;32.95,6.07,;31.92,7.22,;32.47,4.61,;33.37,3.36,;32.44,2.11,;30.99,2.61,;30.99,4.14,;29.68,4.91,;29.62,6.47,;28.37,4.08,;28.43,2.53,;29.81,1.83,;29.87,.29,;31.25,-.44,;31.32,-1.99,;32.69,-2.69,;30.02,-2.82,;26.99,4.81,;25.69,3.97,;25.76,2.41,;24.33,4.68,;24.25,6.23,;25.54,7.06,;26.92,6.35,;25.48,8.6,;23.01,3.84,;21.63,4.56,;21.57,6.12,;20.32,3.73,;20.41,2.18,;21.76,1.47,;23.3,1.54,;23.85,.09,;22.66,-.87,;22.56,-2.4,;21.21,-3.08,;19.9,-2.25,;20,-.71,;21.38,-.02,;18.96,4.45,;17.66,3.62,;17.72,2.06,;16.28,4.33,;16.22,5.86,;17.52,6.71,;18.9,5.99,;20.19,6.83,;20.13,8.36,;21.44,9.2,;18.75,9.08,;17.43,8.25,;14.97,3.49,;13.59,4.21,;13.52,5.75,;12.3,3.37,;12.37,1.83,;13.74,1.12,;10.92,4.1,;9.61,3.27,;9.68,1.71,;8.23,3.97,;8.17,5.51,;7.08,6.61,;5.53,6.54,;4.97,7.98,;6.17,8.95,;6.25,10.48,;7.62,11.19,;8.91,10.35,;8.83,8.81,;7.47,8.11,;6.94,3.14,;5.56,3.84,;5.48,5.38,;4.26,3.01,;4.32,1.47,;5.7,.77,;6.98,1.6,;8.35,.9,;8.43,-.64,;7.13,-1.48,;5.77,-.77,;2.88,3.73,;1.57,2.89,;1.63,1.34,;.22,3.62,;.21,5.16,;-1.26,5.62,;-2.16,4.37,;-3.7,4.36,;-1.25,3.14,)|
Show InChI InChI=1S/C67H85N15O12/c1-4-70-65(93)56-21-13-29-82(56)66(94)49(20-12-28-71-67(68)69)75-59(87)50(30-38(2)3)76-62(90)53(33-41-35-72-46-18-10-8-16-44(41)46)79-61(89)52(32-40-22-24-43(84)25-23-40)78-64(92)55(37-83)81-63(91)54(34-42-36-73-47-19-11-9-17-45(42)47)80-60(88)51(31-39-14-6-5-7-15-39)77-58(86)48-26-27-57(85)74-48/h5-11,14-19,22-25,35-36,38,48-56,72-73,83-84H,4,12-13,20-21,26-34,37H2,1-3H3,(H,70,93)(H,74,85)(H,75,87)(H,76,90)(H,77,86)(H,78,92)(H,79,89)(H,80,88)(H,81,91)(H4,68,69,71)/t48-,49-,50-,51-,52-,53+,54-,55-,56-/m0/s1
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UniChem
Article
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0.0250n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470101
PNG
(CHEMBL406887)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](CCCCNC(=O)c1cccnc1)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1cccc(F)c1 |wU:61.66,12.20,wD:23.28,31.46,5.4,67.70,48.50,(28.94,-13.15,;28.96,-14.67,;27.64,-15.47,;26.3,-14.7,;25,-15.47,;26.27,-13.19,;27.48,-12.31,;26.95,-10.87,;25.43,-10.87,;25.01,-12.32,;23.68,-13.06,;23.66,-14.61,;22.34,-12.31,;22.36,-10.76,;23.69,-10,;23.71,-8.45,;25.04,-7.7,;25.07,-6.16,;26.4,-5.39,;23.72,-5.38,;21.02,-13.06,;19.69,-12.29,;19.7,-10.74,;18.34,-13.03,;18.33,-14.57,;19.66,-15.37,;20.99,-14.6,;19.63,-16.89,;17.01,-12.25,;15.67,-13.02,;15.67,-14.54,;14.35,-12.24,;14.44,-10.71,;13.22,-9.74,;13.74,-8.29,;12.38,-7.26,;13.05,-5.87,;12.19,-4.58,;12.86,-3.19,;10.61,-4.71,;9.77,-3.43,;8.19,-3.55,;7.55,-4.93,;8.44,-6.22,;9.97,-6.09,;13.02,-13,;11.67,-12.22,;11.67,-10.68,;10.34,-12.98,;10.32,-14.51,;11.64,-15.3,;11.64,-16.85,;12.98,-17.62,;14.32,-16.86,;15.64,-17.63,;14.34,-15.31,;13,-14.54,;9.02,-12.19,;9.03,-10.64,;7.68,-12.95,;7.67,-14.51,;6.36,-12.18,;6.36,-10.64,;7.7,-9.89,;5,-12.93,;3.68,-12.16,;3.71,-10.63,;2.33,-12.92,;2.33,-14.47,;3.65,-15.25,;5.07,-14.63,;6.1,-15.77,;5.32,-17.11,;5.78,-18.57,;4.75,-19.7,;3.23,-19.37,;2.77,-17.91,;3.81,-16.79,;1.01,-12.16,;-.32,-12.9,;-.29,-14.43,;-1.7,-12.19,;-3.11,-13.15,;-4.66,-12.38,;-4.79,-10.64,;-6.31,-9.9,;-7.75,-10.87,;-7.63,-12.6,;-9.12,-13.5,;-6.08,-13.35,)|
Show InChI InChI=1S/C64H85FN14O11/c1-5-69-60(87)53-21-13-31-79(53)63(90)49(20-12-30-71-64(66)67)75-58(85)50(32-39(2)3)76-57(84)48(19-8-9-29-70-56(83)42-15-11-28-68-36-42)74-61(88)54(34-41-22-25-45(81)26-23-41)78(4)62(89)52(38-80)77-59(86)51(35-43-37-72-47-18-7-6-17-46(43)47)73-55(82)27-24-40-14-10-16-44(65)33-40/h6-7,10-11,14-18,22-23,25-26,28,33,36-37,39,48-54,72,80-81H,5,8-9,12-13,19-21,24,27,29-32,34-35,38H2,1-4H3,(H,69,87)(H,70,83)(H,73,82)(H,74,88)(H,75,85)(H,76,84)(H,77,86)(H4,66,67,71)/t48-,49+,50+,51+,52+,53-,54+/m1/s1
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Article
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0.0260n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470127
PNG
(CHEMBL2369141)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:57.63,12.20,63.67,wD:45.57,31.44,23.28,5.4,(37.09,-9.27,;37.09,-10.82,;35.77,-11.59,;34.44,-10.84,;33.14,-11.59,;34.41,-9.34,;35.61,-8.44,;35.1,-7.01,;33.59,-7.01,;33.16,-8.46,;31.82,-9.21,;31.82,-10.74,;30.5,-8.44,;30.5,-6.89,;31.85,-6.14,;31.85,-4.61,;33.2,-3.84,;33.2,-2.32,;34.54,-1.55,;31.88,-1.52,;29.17,-9.2,;27.83,-8.43,;27.85,-6.88,;26.5,-9.18,;26.48,-10.71,;27.82,-11.49,;27.8,-13.04,;29.15,-10.72,;25.16,-8.4,;23.84,-9.14,;23.83,-10.69,;22.52,-8.37,;22.52,-6.85,;22.06,-5.38,;20.59,-4.9,;20.59,-3.36,;22.07,-2.89,;22.68,-1.49,;24.23,-1.33,;25.13,-2.58,;24.48,-4,;22.96,-4.15,;21.19,-9.14,;19.85,-8.36,;19.85,-6.83,;18.5,-9.11,;18.5,-10.66,;19.82,-11.43,;19.82,-12.97,;21.14,-13.74,;22.49,-13,;23.81,-13.76,;22.49,-11.46,;21.17,-10.68,;17.18,-8.34,;15.87,-9.08,;15.83,-10.62,;14.54,-8.31,;14.55,-6.8,;15.87,-6.02,;13.2,-9.08,;11.87,-8.31,;11.88,-6.76,;10.53,-9.05,;10.52,-10.59,;11.85,-11.38,;13.26,-10.75,;14.28,-11.91,;13.49,-13.23,;13.96,-14.71,;12.93,-15.83,;11.43,-15.51,;10.95,-14.03,;12,-12.91,;9.21,-8.3,;7.86,-9.05,;7.89,-10.56,;6.51,-8.31,;5.08,-9.27,;3.54,-8.52,;3.42,-6.8,;1.88,-6.05,;.45,-7.01,;-1.05,-6.17,;.58,-8.73,;2.12,-9.47,)|
Show InChI InChI=1S/C62H78FN13O10/c1-4-66-60(85)53-16-10-28-76(53)61(86)47(15-9-27-67-62(64)65)71-55(80)48(29-36(2)3)72-58(83)51(32-40-34-69-46-14-8-6-12-44(40)46)74-56(81)49(30-38-19-24-42(78)25-20-38)73-59(84)52(35-77)75-57(82)50(31-39-33-68-45-13-7-5-11-43(39)45)70-54(79)26-21-37-17-22-41(63)23-18-37/h5-8,11-14,17-20,22-25,33-34,36,47-53,68-69,77-78H,4,9-10,15-16,21,26-32,35H2,1-3H3,(H,66,85)(H,70,79)(H,71,80)(H,72,83)(H,73,84)(H,74,81)(H,75,82)(H4,64,65,67)/t47-,48-,49-,50+,51+,52-,53+/m0/s1
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UniChem
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0.0290n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470121
PNG
(CHEMBL268173)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCCNC(=O)c1cccnc1)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccnc1)NC(=O)[C@H](Cc1ccc(Cl)cc1)NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(C)=O)C(=O)N[C@@H](CCCCNC(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@@H](C)C(N)=O
Show InChI InChI=1S/C80H104ClN15O14/c1-48(2)39-63(73(103)90-62(22-11-12-36-85-49(3)4)80(110)96-38-16-23-68(96)77(107)87-50(5)70(82)100)91-72(102)61(21-10-13-37-86-71(101)58-20-15-35-84-46-58)89-78(108)69(44-53-27-32-60(99)33-28-53)95(7)79(109)67(47-97)94-76(106)66(43-55-17-14-34-83-45-55)93-75(105)65(41-52-25-30-59(81)31-26-52)92-74(104)64(88-51(6)98)42-54-24-29-56-18-8-9-19-57(56)40-54/h8-9,14-15,17-20,24-35,40,45-46,48-50,61-69,85,97,99H,10-13,16,21-23,36-39,41-44,47H2,1-7H3,(H2,82,100)(H,86,101)(H,87,107)(H,88,98)(H,89,108)(H,90,103)(H,91,102)(H,92,104)(H,93,105)(H,94,106)/t50-,61-,62-,63-,64+,65-,66-,67-,68+,69-/m0/s1
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0.0320n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470079
PNG
(CHEMBL445681)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:58.64,12.20,wD:31.44,23.28,5.4,64.68,45.48,(26.52,-7.4,;26.53,-8.93,;25.21,-9.72,;23.86,-8.96,;22.57,-9.72,;23.83,-7.45,;25.05,-6.57,;24.54,-5.13,;23.01,-5.13,;22.57,-6.58,;21.25,-7.32,;21.24,-8.86,;19.92,-6.57,;19.93,-5.02,;21.28,-4.26,;21.29,-2.71,;22.63,-1.96,;22.64,-.43,;23.96,.34,;21.31,.35,;18.58,-7.32,;17.26,-6.54,;17.26,-5,;15.91,-7.28,;15.91,-8.83,;17.23,-9.62,;18.57,-8.85,;17.22,-11.15,;14.59,-6.51,;13.26,-7.27,;13.24,-8.8,;11.94,-6.5,;11.95,-4.97,;11.47,-3.51,;10.02,-3.03,;10.02,-1.48,;11.49,-1.01,;12.11,.39,;13.65,.55,;14.55,-.69,;13.92,-2.1,;12.37,-2.26,;10.6,-7.25,;9.27,-6.48,;9.27,-4.94,;7.93,-7.24,;7.92,-8.77,;9.24,-9.56,;10.59,-8.8,;11.92,-9.57,;11.91,-11.12,;13.23,-11.89,;10.57,-11.88,;9.24,-11.1,;6.61,-6.45,;6.61,-4.9,;5.28,-7.21,;5.26,-8.77,;3.94,-6.44,;3.96,-4.9,;5.29,-4.15,;2.61,-7.19,;1.27,-6.42,;1.3,-4.89,;-.06,-7.18,;-.09,-8.72,;1.26,-9.51,;2.67,-8.88,;3.68,-10.02,;2.91,-11.36,;3.36,-12.82,;2.33,-13.95,;.84,-13.63,;.36,-12.17,;1.39,-11.04,;-1.38,-6.42,;-2.73,-7.16,;-2.73,-8.69,;-4.08,-6.42,;-5.53,-7.35,;-7.05,-6.58,;-8.49,-7.51,;-10.03,-6.74,;-10.13,-5.02,;-11.64,-4.16,;-8.68,-4.09,;-7.15,-4.87,)|
Show InChI InChI=1S/C63H80FN13O10/c1-5-67-59(84)53-17-11-29-77(53)62(87)48(16-10-28-68-63(65)66)72-56(81)49(30-37(2)3)73-58(83)51(33-41-35-70-47-15-9-7-13-45(41)47)74-60(85)54(31-39-20-25-43(79)26-21-39)76(4)61(86)52(36-78)75-57(82)50(32-40-34-69-46-14-8-6-12-44(40)46)71-55(80)27-22-38-18-23-42(64)24-19-38/h6-9,12-15,18-21,23-26,34-35,37,48-54,69-70,78-79H,5,10-11,16-17,22,27-33,36H2,1-4H3,(H,67,84)(H,71,80)(H,72,81)(H,73,83)(H,74,85)(H,75,82)(H4,65,66,68)/t48-,49-,50-,51+,52-,53+,54-/m0/s1
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0.0330n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470124
PNG
(CHEMBL437632)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.67,(28.48,-7.02,;28.49,-8.55,;27.17,-9.33,;25.82,-8.56,;24.53,-9.33,;25.79,-7.07,;27.01,-6.18,;26.49,-4.74,;24.97,-4.76,;24.53,-6.18,;23.22,-6.94,;23.21,-8.46,;21.89,-6.18,;21.9,-4.64,;23.24,-3.87,;23.25,-2.35,;24.59,-1.59,;24.6,-.04,;25.92,.71,;23.27,.73,;20.55,-6.92,;19.23,-6.15,;19.23,-4.61,;17.88,-6.91,;17.88,-8.45,;19.2,-9.23,;19.19,-10.77,;20.54,-8.46,;16.56,-6.14,;15.23,-6.89,;15.21,-8.42,;13.92,-6.12,;13.93,-4.57,;13.45,-3.13,;12,-2.65,;12,-1.1,;13.47,-.62,;14.09,.76,;15.62,.92,;16.52,-.32,;15.89,-1.74,;14.35,-1.87,;12.58,-6.88,;11.25,-6.09,;11.25,-4.56,;9.91,-6.86,;9.9,-8.39,;11.22,-9.17,;11.22,-10.71,;12.55,-11.48,;13.88,-10.73,;15.2,-11.48,;13.9,-9.19,;12.57,-8.4,;8.59,-6.07,;7.26,-6.82,;7.24,-8.37,;5.92,-6.05,;5.95,-4.53,;7.27,-3.77,;4.6,-6.81,;3.26,-6.04,;3.29,-4.51,;1.93,-6.79,;1.91,-8.34,;3.25,-9.11,;4.66,-8.5,;5.67,-9.64,;4.9,-10.97,;5.35,-12.44,;4.32,-13.56,;2.83,-13.24,;2.36,-11.77,;3.39,-10.65,;.61,-6.02,;-.73,-6.76,;-.71,-8.29,;-2.09,-6.04,;-3.52,-6.99,;-5.07,-6.21,;-5.16,-4.51,;-6.71,-3.74,;-8.13,-4.7,;-9.64,-3.86,;-8.02,-6.41,;-6.48,-7.18,)|
Show InChI InChI=1S/C62H78FN13O10/c1-4-66-60(85)53-16-10-28-76(53)61(86)47(15-9-27-67-62(64)65)71-55(80)48(29-36(2)3)72-58(83)51(32-40-34-69-46-14-8-6-12-44(40)46)74-56(81)49(30-38-19-24-42(78)25-20-38)73-59(84)52(35-77)75-57(82)50(31-39-33-68-45-13-7-5-11-43(39)45)70-54(79)26-21-37-17-22-41(63)23-18-37/h5-8,11-14,17-20,22-25,33-34,36,47-53,68-69,77-78H,4,9-10,15-16,21,26-32,35H2,1-3H3,(H,66,85)(H,70,79)(H,71,80)(H,72,83)(H,73,84)(H,74,81)(H,75,82)(H4,64,65,67)/t47-,48-,49-,50-,51+,52-,53+/m0/s1
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0.0330n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470107
PNG
(CHEMBL2371292)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:55.60,43.54,12.20,61.64,wD:31.41,23.28,5.4,(-4.86,4.47,;-3.76,3.4,;-4.14,1.91,;-3.04,.83,;-1.56,1.25,;-3.42,-.66,;-4.85,-1.23,;-4.76,-2.77,;-3.26,-3.15,;-2.44,-1.85,;-.9,-1.75,;-.22,-.37,;-.05,-3.03,;-.73,-4.41,;-2.27,-4.51,;-2.95,-5.89,;-4.49,-5.99,;-5.17,-7.37,;-6.71,-7.47,;-4.32,-8.65,;1.49,-2.93,;2.34,-4.21,;1.66,-5.59,;3.88,-4.12,;4.56,-2.74,;3.71,-1.45,;2.17,-1.55,;4.39,-.07,;4.73,-5.4,;6.27,-5.3,;6.95,-3.92,;7.12,-6.58,;6.44,-7.96,;4.9,-8.06,;4.05,-6.78,;2.51,-6.88,;1.83,-8.26,;.29,-8.35,;2.68,-9.54,;4.22,-9.44,;8.66,-6.48,;9.51,-7.76,;8.83,-9.14,;11.05,-7.66,;11.73,-6.28,;10.88,-5,;11.56,-3.62,;10.71,-2.34,;9.17,-2.44,;8.32,-1.16,;8.49,-3.82,;9.34,-5.1,;11.9,-8.95,;13.44,-8.85,;14.12,-7.47,;14.29,-10.13,;13.61,-11.51,;12.07,-11.61,;15.83,-10.03,;16.69,-11.31,;16,-12.69,;18.22,-11.21,;19.08,-12.5,;20.61,-12.4,;21.6,-13.58,;23.03,-13.01,;22.93,-11.48,;24,-10.37,;23.59,-8.89,;22.1,-8.51,;21.02,-9.61,;21.44,-11.1,;18.91,-9.83,;18.05,-8.55,;16.51,-8.65,;18.73,-7.17,;17.88,-5.89,;18.56,-4.51,;17.71,-3.23,;18.39,-1.85,;19.93,-1.75,;20.61,-.37,;20.78,-3.03,;20.1,-4.41,)|
Show InChI InChI=1S/C60H77FN12O11/c1-4-64-58(83)51-12-8-28-73(51)59(84)45(11-7-27-65-60(62)63)68-53(78)46(29-35(2)3)69-54(79)47(30-37-15-22-41(75)23-16-37)70-55(80)48(31-38-17-24-42(76)25-18-38)71-57(82)50(34-74)72-56(81)49(32-39-33-66-44-10-6-5-9-43(39)44)67-52(77)26-19-36-13-20-40(61)21-14-36/h5-6,9-10,13-18,20-25,33,35,45-51,66,74-76H,4,7-8,11-12,19,26-32,34H2,1-3H3,(H,64,83)(H,67,77)(H,68,78)(H,69,79)(H,70,80)(H,71,82)(H,72,81)(H4,62,63,65)/t45-,46-,47+,48+,49-,50-,51+/m0/s1
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0.0380n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470122
PNG
(CHEMBL265538)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1F |wU:58.64,12.20,wD:31.44,23.28,5.4,64.68,45.48,(29.19,-5.42,;29.2,-6.96,;27.88,-7.74,;26.52,-6.97,;25.23,-7.74,;26.49,-5.48,;27.71,-4.59,;27.2,-3.14,;25.67,-3.16,;25.23,-4.59,;23.91,-5.35,;23.9,-6.87,;22.58,-4.59,;22.59,-3.04,;23.93,-2.27,;23.95,-.74,;25.29,.02,;25.3,1.57,;26.62,2.32,;23.97,2.34,;21.24,-5.33,;19.92,-4.55,;19.92,-3.01,;18.57,-5.32,;18.57,-6.86,;19.89,-7.65,;21.23,-6.87,;19.88,-9.18,;17.24,-4.54,;15.91,-5.29,;15.89,-6.83,;14.59,-4.52,;14.6,-2.97,;14.12,-1.52,;12.67,-1.04,;12.67,.5,;14.14,.99,;14.76,2.37,;16.3,2.53,;17.2,1.29,;16.56,-.13,;15.02,-.27,;13.25,-5.28,;11.92,-4.49,;11.92,-2.96,;10.58,-5.26,;10.57,-6.8,;11.89,-7.58,;13.24,-6.81,;14.57,-7.6,;14.54,-9.15,;15.88,-9.9,;13.22,-9.9,;11.89,-9.13,;9.26,-4.48,;9.26,-2.93,;7.9,-5.23,;7.9,-6.78,;6.58,-4.46,;6.6,-2.93,;7.94,-2.17,;5.25,-5.22,;3.91,-4.45,;3.94,-2.91,;2.58,-5.2,;2.56,-6.74,;3.9,-7.52,;5.32,-6.9,;6.32,-8.05,;5.55,-9.38,;6,-10.86,;4.97,-11.98,;3.48,-11.66,;3.01,-10.19,;4.04,-9.06,;1.26,-4.42,;-.09,-5.16,;-.12,-6.7,;-1.41,-4.39,;-2.89,-5.26,;-4.38,-4.42,;-4.41,-2.72,;-5.92,-1.88,;-7.4,-2.75,;-8.86,-1.85,;-7.37,-4.49,;-5.85,-5.33,;-5.48,-7,)|
Show InChI InChI=1S/C63H79F2N13O10/c1-5-68-59(85)53-17-11-27-78(53)62(88)48(16-10-26-69-63(66)67)73-56(82)49(28-36(2)3)74-58(84)51(31-40-34-71-47-15-9-7-13-44(40)47)75-60(86)54(29-37-18-23-42(80)24-19-37)77(4)61(87)52(35-79)76-57(83)50(30-39-33-70-46-14-8-6-12-43(39)46)72-55(81)25-21-38-20-22-41(64)32-45(38)65/h6-9,12-15,18-20,22-24,32-34,36,48-54,70-71,79-80H,5,10-11,16-17,21,25-31,35H2,1-4H3,(H,68,85)(H,72,81)(H,73,82)(H,74,84)(H,75,86)(H,76,83)(H4,66,67,69)/t48-,49-,50-,51+,52-,53+,54-/m0/s1
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0.0390n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470103
PNG
(CHEMBL384341)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1F |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.67,(23.78,-1.33,;23.78,-2.87,;22.46,-3.65,;21.13,-2.88,;19.82,-3.65,;21.1,-1.38,;22.3,-.49,;21.78,.96,;20.27,.96,;19.84,-.49,;18.5,-1.26,;18.5,-2.78,;17.18,-.49,;17.18,1.05,;18.53,1.82,;18.53,3.35,;19.88,4.12,;19.88,5.66,;21.22,6.41,;18.56,6.43,;15.85,-1.23,;14.5,-.46,;14.53,1.08,;13.17,-1.22,;13.15,-2.75,;14.49,-3.55,;14.47,-5.09,;15.82,-2.78,;11.83,-.45,;10.51,-1.2,;10.5,-2.74,;9.19,-.43,;9.19,1.12,;8.73,2.57,;7.26,3.05,;7.26,4.59,;8.74,5.08,;9.35,6.46,;10.9,6.62,;11.8,5.38,;11.15,3.96,;9.63,3.82,;7.86,-1.19,;6.52,-.4,;6.52,1.13,;5.16,-1.17,;5.16,-2.71,;6.48,-3.49,;6.48,-5.04,;7.8,-5.81,;9.16,-5.06,;10.48,-5.81,;9.16,-3.51,;7.84,-2.72,;3.84,-.39,;2.52,-1.14,;2.49,-2.68,;1.19,-.37,;1.2,1.16,;2.52,1.92,;-.15,-1.13,;-1.48,-.35,;-1.47,1.18,;-2.82,-1.11,;-2.83,-2.65,;-1.5,-3.42,;-.09,-2.81,;.93,-3.96,;.14,-5.29,;.61,-6.76,;-.42,-7.89,;-1.92,-7.57,;-2.4,-6.1,;-1.35,-4.97,;-4.14,-.33,;-5.5,-1.11,;-5.44,-2.62,;-6.85,-.39,;-8.28,-1.35,;-9.82,-.59,;-9.94,1.13,;-11.49,1.89,;-12.94,.92,;-14.43,1.76,;-12.81,-.81,;-11.24,-1.56,;-10.78,-3.22,)|
Show InChI InChI=1S/C62H77F2N13O10/c1-4-67-60(86)53-16-10-26-77(53)61(87)47(15-9-25-68-62(65)66)72-55(81)48(27-35(2)3)73-58(84)51(30-39-33-70-46-14-8-6-12-43(39)46)75-56(82)49(28-36-17-22-41(79)23-18-36)74-59(85)52(34-78)76-57(83)50(29-38-32-69-45-13-7-5-11-42(38)45)71-54(80)24-20-37-19-21-40(63)31-44(37)64/h5-8,11-14,17-19,21-23,31-33,35,47-53,69-70,78-79H,4,9-10,15-16,20,24-30,34H2,1-3H3,(H,67,86)(H,71,80)(H,72,81)(H,73,84)(H,74,85)(H,75,82)(H,76,83)(H4,65,66,68)/t47-,48-,49-,50-,51+,52-,53+/m0/s1
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0.0400n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470130
PNG
(CHEMBL217175)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:58.64,12.20,wD:31.44,23.28,5.4,64.81,45.48,(29.62,-3.96,;29.63,-5.48,;28.31,-6.27,;26.96,-5.51,;25.67,-6.27,;26.93,-4,;28.15,-3.12,;27.64,-1.68,;26.09,-1.68,;25.67,-3.13,;24.36,-3.87,;24.35,-5.41,;23.03,-3.12,;23.04,-1.58,;24.38,-.81,;24.39,.73,;25.73,1.48,;25.74,3.01,;27.06,3.78,;24.41,3.79,;21.69,-3.87,;20.37,-3.1,;20.37,-1.55,;19.02,-3.84,;19.02,-5.38,;20.34,-6.17,;21.68,-5.4,;20.33,-7.7,;17.7,-3.07,;16.37,-3.83,;16.35,-5.35,;15.05,-3.06,;15.06,-1.52,;14.58,-.06,;13.13,.42,;13.13,1.96,;14.6,2.43,;15.22,3.83,;16.76,3.99,;17.66,2.75,;17.02,1.34,;15.48,1.18,;13.71,-3.81,;12.38,-3.03,;12.38,-1.49,;11.04,-3.79,;11.04,-5.32,;12.36,-6.11,;13.7,-5.35,;15.03,-6.12,;15.02,-7.66,;16.34,-8.44,;13.68,-8.43,;12.35,-7.65,;9.72,-3,;9.72,-1.46,;8.39,-3.76,;8.37,-5.32,;7.05,-2.99,;7.08,-1.46,;8.4,-.71,;5.72,-3.74,;4.38,-2.97,;4.42,-1.45,;3.06,-3.73,;3.06,-5.27,;4.37,-6.08,;5.74,-5.34,;7.05,-6.12,;6.99,-7.66,;5.64,-8.4,;5.64,-9.95,;4.29,-10.69,;2.97,-9.91,;2.99,-8.36,;4.34,-7.62,;1.74,-2.97,;.4,-3.71,;.43,-5.24,;-.99,-3,;-2.4,-3.97,;-3.94,-3.23,;-5.36,-4.19,;-6.9,-3.45,;-7.03,-1.74,;-8.55,-.91,;-5.62,-.77,;-4.07,-1.51,)|
Show InChI InChI=1S/C65H81FN12O10/c1-5-69-61(85)55-20-12-32-78(55)64(88)50(19-11-31-70-65(67)68)73-58(82)51(33-39(2)3)74-60(84)53(36-44-37-71-49-18-9-8-17-48(44)49)75-62(86)56(34-41-23-28-46(80)29-24-41)77(4)63(87)54(38-79)76-59(83)52(35-43-15-10-14-42-13-6-7-16-47(42)43)72-57(81)30-25-40-21-26-45(66)27-22-40/h6-10,13-18,21-24,26-29,37,39,50-56,71,79-80H,5,11-12,19-20,25,30-36,38H2,1-4H3,(H,69,85)(H,72,81)(H,73,82)(H,74,84)(H,75,86)(H,76,83)(H4,67,68,70)/t50-,51-,52-,53+,54-,55+,56-/m0/s1
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0.0480n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470078
PNG
(CHEMBL413393)
Show SMILES [#6]-[#8]-c1ccc(cc1)-[#6](=O)-[#6]-[#6]-[#6@H](-[#7]-[#6](=O)-[#6@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#7]-[#6](=O)-[#6@H](-[#6]-[#8])-[#7]-[#6](=O)-[#6@H](-[#6]-c1cccnc1)-[#7]-[#6](=O)-[#6@H](-[#6]-c1ccc(Cl)cc1)-[#7]-[#6](=O)-[#6@@H](-[#6]-c1ccc2ccccc2c1)-[#7]-[#6](-[#6])=O)-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6](-[#6])-[#6])-[#6](=O)-[#7]-[#6@@H](-[#6]-[#6]-[#6]\[#7]=[#6](\[#7])-[#7])-[#6](=O)-[#7]-1-[#6]-[#6]-[#6]-[#6@@H]-1-[#6](=O)-[#7]-[#6@@H](-[#6])-[#6](-[#7])=O
Show InChI InChI=1S/C73H97ClN18O14/c1-41(2)34-55(65(99)87-54(16-10-32-82-73(78)79)71(105)92-33-11-17-60(92)70(104)83-42(3)62(75)96)88-64(98)53(28-29-61(95)48-22-26-51(106-5)27-23-48)86-63(97)52(15-9-31-81-72(76)77)85-69(103)59(40-93)91-68(102)58(38-46-12-8-30-80-39-46)90-67(101)57(36-44-19-24-50(74)25-20-44)89-66(100)56(84-43(4)94)37-45-18-21-47-13-6-7-14-49(47)35-45/h6-8,12-14,18-27,30,35,39,41-42,52-60,93H,9-11,15-17,28-29,31-34,36-38,40H2,1-5H3,(H2,75,96)(H,83,104)(H,84,94)(H,85,103)(H,86,97)(H,87,99)(H,88,98)(H,89,100)(H,90,101)(H,91,102)(H4,76,77,81)(H4,78,79,82)/t42-,52-,53-,54-,55-,56+,57-,58-,59-,60+/m0/s1
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0.0520n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470092
PNG
(CHEMBL428138)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)C(Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(Cl)cc1 |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,(33.55,-8.61,;33.56,-10.16,;32.24,-10.93,;30.9,-10.18,;29.61,-10.93,;30.86,-8.68,;32.08,-7.78,;31.57,-6.36,;30.05,-6.36,;29.61,-7.8,;28.3,-8.55,;28.28,-10.08,;26.97,-7.78,;26.98,-6.24,;28.3,-5.49,;28.33,-3.96,;29.66,-3.19,;29.68,-1.67,;30.99,-.91,;28.35,-.88,;25.63,-8.54,;24.31,-7.77,;24.31,-6.23,;22.97,-8.52,;22.97,-10.05,;24.28,-10.83,;24.27,-12.37,;25.62,-10.06,;21.65,-7.75,;20.32,-8.49,;20.3,-10.03,;19.01,-7.72,;19.02,-6.2,;18.54,-4.73,;17.09,-4.25,;17.09,-2.71,;18.56,-2.25,;19.18,-.85,;20.71,-.68,;21.61,-1.94,;20.98,-3.35,;19.43,-3.5,;17.67,-8.49,;16.34,-7.71,;16.34,-6.17,;15,-8.45,;14.99,-10,;16.31,-10.77,;16.31,-12.31,;17.64,-13.08,;18.97,-12.34,;20.29,-13.1,;18.98,-10.8,;17.66,-10.02,;13.69,-7.68,;12.36,-8.42,;12.34,-9.98,;11.02,-7.65,;11.04,-6.14,;12.37,-5.37,;9.7,-8.42,;8.36,-7.65,;8.39,-6.11,;7.03,-8.39,;7.01,-9.93,;8.35,-10.72,;9.76,-10.09,;10.77,-11.25,;10,-12.56,;10.44,-14.04,;9.42,-15.16,;7.93,-14.84,;7.46,-13.37,;8.49,-12.24,;5.71,-7.64,;4.38,-8.39,;4.34,-9.9,;3.03,-7.62,;1.58,-8.54,;.07,-7.72,;.01,-6.01,;-1.5,-5.21,;-2.95,-6.11,;-4.43,-5.24,;-2.89,-7.84,;-1.37,-8.64,)|
Show InChI InChI=1S/C62H78ClN13O10/c1-4-66-60(85)53-16-10-28-76(53)61(86)47(15-9-27-67-62(64)65)71-55(80)48(29-36(2)3)72-58(83)51(32-40-34-69-46-14-8-6-12-44(40)46)74-56(81)49(30-38-19-24-42(78)25-20-38)73-59(84)52(35-77)75-57(82)50(31-39-33-68-45-13-7-5-11-43(39)45)70-54(79)26-21-37-17-22-41(63)23-18-37/h5-8,11-14,17-20,22-25,33-34,36,47-53,68-69,77-78H,4,9-10,15-16,21,26-32,35H2,1-3H3,(H,66,85)(H,70,79)(H,71,80)(H,72,83)(H,73,84)(H,74,81)(H,75,82)(H4,64,65,67)/t47-,48-,49-,50?,51+,52-,53+/m0/s1
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0.0520n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470089
PNG
(CHEMBL429365)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)c(F)c1 |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.67,(30.24,-8.6,;30.26,-10.14,;28.94,-10.91,;27.6,-10.16,;26.31,-10.91,;27.57,-8.66,;28.78,-7.76,;28.27,-6.34,;26.73,-6.34,;26.32,-7.78,;24.99,-8.53,;24.97,-10.07,;23.65,-7.76,;23.67,-6.22,;25,-5.47,;25.02,-3.93,;26.35,-3.16,;26.37,-1.64,;27.7,-.88,;25.03,-.85,;22.33,-8.52,;21,-7.75,;21.01,-6.21,;19.66,-8.5,;19.65,-10.03,;20.98,-10.82,;20.95,-12.36,;22.3,-10.04,;18.33,-7.73,;16.99,-8.47,;16.99,-10.01,;15.67,-7.7,;15.69,-6.17,;15.22,-4.71,;13.76,-4.22,;13.76,-2.68,;15.22,-2.22,;15.85,-.81,;17.38,-.65,;18.28,-1.91,;17.66,-3.32,;16.12,-3.47,;14.35,-8.47,;13,-7.69,;13,-6.15,;11.67,-8.44,;11.67,-9.98,;12.99,-10.75,;12.97,-12.3,;14.31,-13.07,;15.64,-12.33,;16.96,-13.09,;15.66,-10.78,;14.32,-10,;10.36,-7.66,;9.02,-8.4,;9,-9.97,;7.7,-7.63,;7.7,-6.12,;9.04,-5.35,;6.35,-8.4,;5.03,-7.63,;5.05,-6.09,;3.68,-8.37,;3.68,-9.92,;5,-10.71,;6.41,-10.08,;7.44,-11.23,;6.66,-12.55,;7.12,-14.03,;6.09,-15.16,;4.58,-14.84,;4.12,-13.36,;5.16,-12.23,;2.36,-7.62,;1.03,-8.37,;1.09,-9.88,;-.34,-7.66,;-1.76,-8.66,;-3.31,-7.94,;-3.46,-6.24,;-5.02,-5.51,;-6.43,-6.51,;-7.96,-5.7,;-6.26,-8.21,;-7.74,-9.14,;-4.72,-8.94,)|
Show InChI InChI=1S/C62H77F2N13O10/c1-4-67-60(86)53-16-10-26-77(53)61(87)47(15-9-25-68-62(65)66)72-55(81)48(27-35(2)3)73-58(84)51(31-39-33-70-46-14-8-6-12-42(39)46)75-56(82)49(29-37-17-21-40(79)22-18-37)74-59(85)52(34-78)76-57(83)50(30-38-32-69-45-13-7-5-11-41(38)45)71-54(80)24-20-36-19-23-43(63)44(64)28-36/h5-8,11-14,17-19,21-23,28,32-33,35,47-53,69-70,78-79H,4,9-10,15-16,20,24-27,29-31,34H2,1-3H3,(H,67,86)(H,71,80)(H,72,81)(H,73,84)(H,74,85)(H,75,82)(H,76,83)(H4,65,66,68)/t47-,48-,49-,50-,51+,52-,53+/m0/s1
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UniChem
Article
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0.0520n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470081
PNG
(CHEMBL267843)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccc2ccccc12)NC(=O)CCc1ccc(Br)cc1 |wU:58.64,12.20,wD:31.44,23.28,5.4,64.81,45.48,(26.5,-8.03,;26.51,-9.57,;25.2,-10.34,;23.85,-9.59,;22.57,-10.34,;23.82,-8.1,;25.04,-7.2,;24.52,-5.77,;23,-5.79,;22.57,-7.22,;21.25,-7.97,;21.24,-9.5,;19.92,-7.2,;19.93,-5.66,;21.27,-4.91,;21.28,-3.38,;22.62,-2.61,;22.63,-1.09,;23.94,-.33,;21.3,-.3,;18.59,-7.96,;17.27,-7.19,;17.27,-5.65,;15.92,-7.94,;15.92,-9.48,;17.24,-10.25,;18.58,-9.48,;17.23,-11.79,;14.61,-7.17,;13.28,-7.9,;13.26,-9.44,;11.97,-7.13,;11.98,-5.61,;11.5,-4.15,;10.05,-3.67,;10.05,-2.13,;11.52,-1.67,;12.14,-.27,;13.67,-.11,;14.57,-1.36,;13.93,-2.77,;12.39,-2.92,;10.63,-7.9,;9.3,-7.12,;9.3,-5.59,;7.97,-7.87,;7.97,-9.41,;9.28,-10.18,;10.62,-9.43,;11.95,-10.21,;11.94,-11.75,;13.25,-12.51,;10.6,-12.49,;9.27,-11.72,;6.65,-7.1,;6.65,-5.56,;5.3,-7.84,;5.3,-9.4,;3.99,-7.07,;4.01,-5.56,;5.34,-4.79,;2.66,-7.84,;1.33,-7.07,;1.36,-5.53,;,-7.81,;,-9.35,;1.32,-10.15,;2.67,-9.41,;3.99,-10.21,;3.92,-11.75,;2.6,-12.49,;2.58,-14.02,;1.23,-14.77,;-.09,-13.97,;-.06,-12.43,;1.28,-11.69,;-1.32,-7.06,;-2.66,-7.81,;-2.66,-9.31,;-4,-7.04,;-5.44,-7.97,;-6.96,-7.17,;-8.41,-8.08,;-9.91,-7.28,;-10,-5.56,;-11.48,-4.69,;-8.53,-4.65,;-7.03,-5.45,)|
Show InChI InChI=1S/C65H81BrN12O10/c1-5-69-61(85)55-20-12-32-78(55)64(88)50(19-11-31-70-65(67)68)73-58(82)51(33-39(2)3)74-60(84)53(36-44-37-71-49-18-9-8-17-48(44)49)75-62(86)56(34-41-23-28-46(80)29-24-41)77(4)63(87)54(38-79)76-59(83)52(35-43-15-10-14-42-13-6-7-16-47(42)43)72-57(81)30-25-40-21-26-45(66)27-22-40/h6-10,13-18,21-24,26-29,37,39,50-56,71,79-80H,5,11-12,19-20,25,30-36,38H2,1-4H3,(H,69,85)(H,72,81)(H,73,82)(H,74,84)(H,75,86)(H,76,83)(H4,67,68,70)/t50-,51-,52-,53+,54-,55+,56-/m0/s1
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Article
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0.0560n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470120
PNG
(CHEMBL405994)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccccc1F |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.67,(29.72,-9.04,;29.72,-10.57,;28.4,-11.36,;27.07,-10.6,;25.76,-11.36,;27.03,-9.09,;28.24,-8.21,;27.72,-6.77,;26.21,-6.77,;25.78,-8.22,;24.44,-8.96,;24.44,-10.5,;23.12,-8.21,;23.12,-6.66,;24.47,-5.9,;24.47,-4.36,;25.82,-3.6,;25.82,-2.07,;27.16,-1.3,;24.5,-1.29,;21.79,-8.96,;20.45,-8.19,;20.47,-6.64,;19.12,-8.93,;19.1,-10.47,;20.44,-11.26,;20.42,-12.79,;21.77,-10.47,;17.78,-8.15,;16.46,-8.91,;16.45,-10.44,;15.14,-8.14,;15.14,-6.61,;14.68,-5.15,;13.21,-4.67,;13.21,-3.12,;14.69,-2.65,;15.3,-1.26,;16.84,-1.09,;17.74,-2.33,;17.1,-3.74,;15.58,-3.91,;13.81,-8.89,;12.47,-8.12,;12.47,-6.58,;11.11,-8.88,;11.11,-10.41,;12.43,-11.2,;12.43,-12.74,;13.75,-13.52,;15.09,-12.76,;16.42,-13.53,;15.1,-11.21,;13.79,-10.44,;9.79,-8.09,;8.46,-8.85,;8.44,-10.41,;7.14,-8.08,;7.16,-6.54,;8.48,-5.79,;5.8,-8.83,;4.47,-8.06,;4.48,-6.53,;3.13,-8.82,;3.12,-10.36,;4.45,-11.15,;5.87,-10.52,;6.89,-11.66,;6.09,-13,;6.57,-14.46,;5.54,-15.59,;4.03,-15.27,;3.55,-13.81,;4.6,-12.68,;1.81,-8.06,;.46,-8.8,;.56,-10.31,;-.92,-8.12,;-2.31,-9.14,;-3.88,-8.43,;-4.06,-6.73,;-5.62,-6.02,;-7.02,-7.03,;-6.84,-8.73,;-5.27,-9.44,;-5.18,-11.17,)|
Show InChI InChI=1S/C62H78FN13O10/c1-4-66-60(85)53-20-12-28-76(53)61(86)47(19-11-27-67-62(64)65)71-55(80)48(29-36(2)3)72-58(83)51(32-40-34-69-46-18-10-7-15-43(40)46)74-56(81)49(30-37-21-24-41(78)25-22-37)73-59(84)52(35-77)75-57(82)50(31-39-33-68-45-17-9-6-14-42(39)45)70-54(79)26-23-38-13-5-8-16-44(38)63/h5-10,13-18,21-22,24-25,33-34,36,47-53,68-69,77-78H,4,11-12,19-20,23,26-32,35H2,1-3H3,(H,66,85)(H,70,79)(H,71,80)(H,72,83)(H,73,84)(H,74,81)(H,75,82)(H4,64,65,67)/t47-,48-,49-,50-,51+,52-,53+/m0/s1
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0.0580n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470119
PNG
(CHEMBL383952)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)N(C)C(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(Cl)cc1 |wU:58.64,12.20,wD:31.44,23.28,5.4,64.68,45.48,(20.14,-1.88,;20.14,-3.42,;18.82,-4.19,;17.5,-3.44,;16.19,-4.19,;17.46,-1.94,;18.66,-1.04,;18.15,.39,;16.64,.38,;16.21,-1.06,;14.87,-1.81,;14.87,-3.34,;13.55,-1.04,;13.55,.5,;14.9,1.25,;14.9,2.79,;16.25,3.56,;16.25,5.08,;17.59,5.84,;14.93,5.87,;12.22,-1.8,;10.88,-1.03,;10.9,.51,;9.55,-1.78,;9.53,-3.32,;10.87,-4.1,;12.2,-3.32,;10.85,-5.64,;8.21,-1.01,;6.89,-1.75,;6.88,-3.29,;5.57,-.98,;5.57,.55,;5.11,2.02,;3.64,2.5,;3.64,4.04,;5.12,4.5,;5.74,5.91,;7.28,6.07,;8.18,4.81,;7.54,3.4,;6.01,3.25,;4.22,-1.75,;2.91,-.96,;2.91,.57,;1.55,-1.72,;1.55,-3.26,;2.87,-4.03,;4.22,-3.28,;5.54,-4.06,;5.53,-5.61,;6.86,-6.37,;4.19,-6.35,;2.87,-5.57,;.24,-.94,;.26,.6,;-1.09,-1.68,;-1.11,-3.25,;-2.41,-.91,;-2.4,.6,;-1.08,1.37,;-3.75,-1.68,;-5.08,-.91,;-5.07,.63,;-6.42,-1.65,;-6.43,-3.19,;-5.1,-3.99,;-3.69,-3.36,;-2.67,-4.51,;-3.46,-5.83,;-2.99,-7.31,;-4.02,-8.44,;-5.52,-8.12,;-6,-6.64,;-4.95,-5.51,;-7.74,-.9,;-9.09,-1.65,;-9.07,-3.16,;-10.44,-.91,;-11.89,-1.84,;-13.4,-1.07,;-14.85,-2.03,;-16.35,-1.25,;-16.47,.47,;-17.96,1.32,;-15.04,1.42,;-13.5,.63,)|
Show InChI InChI=1S/C63H80ClN13O10/c1-5-67-59(84)53-17-11-29-77(53)62(87)48(16-10-28-68-63(65)66)72-56(81)49(30-37(2)3)73-58(83)51(33-41-35-70-47-15-9-7-13-45(41)47)74-60(85)54(31-39-20-25-43(79)26-21-39)76(4)61(86)52(36-78)75-57(82)50(32-40-34-69-46-14-8-6-12-44(40)46)71-55(80)27-22-38-18-23-42(64)24-19-38/h6-9,12-15,18-21,23-26,34-35,37,48-54,69-70,78-79H,5,10-11,16-17,22,27-33,36H2,1-4H3,(H,67,84)(H,71,80)(H,72,81)(H,73,83)(H,74,85)(H,75,82)(H4,65,66,68)/t48-,49-,50-,51+,52-,53+,54-/m0/s1
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0.0710n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470114
PNG
(CHEMBL268620)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)CCc1ccc(Cl)cc1 |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.76,(26.47,-8.93,;26.47,-10.46,;25.15,-11.24,;23.82,-10.47,;22.51,-11.24,;23.79,-8.98,;24.99,-8.09,;24.47,-6.64,;22.96,-6.64,;22.53,-8.09,;21.19,-8.85,;21.19,-10.37,;19.87,-8.09,;19.87,-6.54,;21.22,-5.77,;21.22,-4.25,;22.57,-3.48,;22.57,-1.94,;23.91,-1.19,;21.25,-1.17,;18.54,-8.83,;17.2,-8.06,;17.22,-6.51,;15.87,-8.82,;15.85,-10.34,;17.19,-11.15,;17.17,-12.68,;18.52,-10.37,;14.53,-8.05,;13.21,-8.8,;13.2,-10.31,;11.89,-8.03,;11.89,-6.48,;11.43,-5.03,;9.96,-4.55,;9.96,-3,;11.44,-2.52,;12.05,-1.14,;13.59,-.98,;14.49,-2.22,;13.85,-3.64,;12.33,-3.78,;10.56,-8.79,;9.22,-7.99,;9.22,-6.47,;7.86,-8.77,;7.86,-10.3,;9.18,-11.08,;10.54,-10.31,;11.86,-11.1,;11.86,-12.65,;13.17,-13.4,;10.5,-13.4,;9.18,-12.63,;6.54,-7.98,;5.22,-8.73,;5.19,-10.28,;3.89,-7.96,;3.91,-6.44,;5.22,-5.68,;2.55,-8.72,;1.22,-7.95,;1.23,-6.42,;-.12,-8.7,;-.12,-10.25,;1.2,-11.05,;2.55,-10.31,;3.87,-11.1,;3.83,-12.65,;5.16,-13.45,;2.48,-13.39,;1.17,-12.6,;-1.44,-7.93,;-2.79,-8.69,;-2.74,-10.21,;-4.14,-7.96,;-5.57,-8.95,;-7.11,-8.19,;-8.53,-9.15,;-10.07,-8.41,;-10.22,-6.69,;-11.74,-5.87,;-8.79,-5.73,;-7.24,-6.48,)|
Show InChI InChI=1S/C60H77ClN12O11/c1-4-64-58(83)51-12-8-28-73(51)59(84)45(11-7-27-65-60(62)63)68-53(78)46(29-35(2)3)69-56(81)49(32-39-33-66-44-10-6-5-9-43(39)44)71-55(80)48(31-38-17-24-42(76)25-18-38)70-57(82)50(34-74)72-54(79)47(30-37-15-22-41(75)23-16-37)67-52(77)26-19-36-13-20-40(61)21-14-36/h5-6,9-10,13-18,20-25,33,35,45-51,66,74-76H,4,7-8,11-12,19,26-32,34H2,1-3H3,(H,64,83)(H,67,77)(H,68,78)(H,69,81)(H,70,82)(H,71,80)(H,72,79)(H4,62,63,65)/t45-,46-,47-,48-,49+,50-,51+/m0/s1
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Article
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0.0760n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470087
PNG
(CHEMBL428093)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(Cl)cc1 |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.67,(30.68,-5.02,;30.68,-6.54,;29.36,-7.34,;28.03,-6.58,;26.73,-7.34,;28,-5.06,;29.2,-4.18,;28.69,-2.75,;27.18,-2.75,;26.75,-4.2,;25.41,-4.94,;25.41,-6.48,;24.09,-4.18,;24.09,-2.64,;25.44,-1.88,;25.44,-.33,;26.79,.42,;26.79,1.95,;28.13,2.73,;25.47,2.74,;22.76,-4.94,;21.41,-4.16,;21.44,-2.62,;20.08,-4.9,;20.06,-6.45,;21.4,-7.24,;21.38,-8.77,;22.73,-6.47,;18.74,-4.13,;17.42,-4.89,;17.41,-6.42,;16.1,-4.12,;16.1,-2.59,;15.64,-1.13,;14.17,-.64,;14.17,.9,;15.65,1.37,;16.26,2.77,;17.81,2.93,;18.71,1.7,;18.07,.28,;16.54,.12,;14.77,-4.87,;13.43,-4.1,;13.43,-2.55,;12.08,-4.86,;12.08,-6.38,;13.4,-7.18,;13.4,-8.72,;14.72,-9.49,;16.07,-8.73,;17.39,-9.51,;16.07,-7.19,;14.75,-6.42,;10.76,-4.07,;9.44,-4.83,;9.41,-6.38,;8.11,-4.06,;8.12,-2.52,;9.44,-1.77,;6.77,-4.81,;5.44,-4.03,;5.45,-2.51,;4.1,-4.8,;4.09,-6.34,;5.42,-7.12,;6.83,-6.5,;7.85,-7.64,;7.06,-8.98,;7.53,-10.44,;6.5,-11.57,;5,-11.24,;4.52,-9.78,;5.57,-8.66,;2.78,-4.03,;1.43,-4.77,;1.45,-6.31,;.08,-4.03,;-1.37,-4.99,;-2.89,-4.2,;-2.98,-2.49,;-4.53,-1.72,;-5.95,-2.65,;-7.46,-1.8,;-5.86,-4.38,;-4.33,-5.15,)|
Show InChI InChI=1S/C62H78ClN13O10/c1-4-66-60(85)53-16-10-28-76(53)61(86)47(15-9-27-67-62(64)65)71-55(80)48(29-36(2)3)72-58(83)51(32-40-34-69-46-14-8-6-12-44(40)46)74-56(81)49(30-38-19-24-42(78)25-20-38)73-59(84)52(35-77)75-57(82)50(31-39-33-68-45-13-7-5-11-43(39)45)70-54(79)26-21-37-17-22-41(63)23-18-37/h5-8,11-14,17-20,22-25,33-34,36,47-53,68-69,77-78H,4,9-10,15-16,21,26-32,35H2,1-3H3,(H,66,85)(H,70,79)(H,71,80)(H,72,83)(H,73,84)(H,74,81)(H,75,82)(H4,64,65,67)/t47-,48-,49-,50-,51+,52-,53+/m0/s1
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0.0760n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470096
PNG
(CHEMBL2369142)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)c1cc2ccccc2[nH]1 |wU:45.57,23.28,5.4,wD:57.63,63.79,31.44,12.20,(20.03,-20.2,;19.55,-18.73,;18.05,-18.41,;17.57,-16.95,;18.6,-15.8,;16.06,-16.63,;14.92,-17.66,;13.58,-16.89,;13.9,-15.38,;15.44,-15.22,;16.21,-13.89,;17.75,-13.89,;15.44,-12.55,;13.9,-12.55,;13.13,-11.22,;11.59,-11.22,;10.82,-12.55,;11.59,-13.89,;10.82,-15.22,;13.13,-13.89,;16.21,-11.22,;15.44,-9.89,;13.9,-9.89,;16.21,-8.55,;17.75,-8.55,;18.52,-9.89,;20.06,-9.89,;17.75,-11.22,;15.44,-7.22,;16.21,-5.88,;17.75,-5.88,;15.44,-4.55,;16.21,-3.22,;17.75,-3.22,;18.65,-4.46,;20.12,-3.99,;20.12,-2.45,;21.26,-1.42,;20.94,.09,;19.48,.57,;18.33,-.46,;18.65,-1.97,;13.9,-4.55,;13.13,-5.88,;13.9,-7.22,;11.59,-5.88,;10.82,-4.55,;11.59,-3.22,;13.13,-3.22,;13.9,-1.88,;13.13,-.55,;13.9,.78,;11.59,-.55,;10.82,-1.88,;10.82,-7.22,;9.28,-7.22,;8.51,-5.88,;8.51,-8.55,;9.28,-9.89,;8.51,-11.22,;6.97,-8.55,;6.2,-9.89,;6.97,-11.22,;4.66,-9.89,;3.89,-8.55,;4.66,-7.22,;6.19,-7.06,;6.51,-5.55,;5.17,-4.78,;4.85,-3.27,;3.39,-2.8,;2.25,-3.83,;2.57,-5.34,;4.03,-5.81,;3.89,-11.22,;2.35,-11.22,;1.58,-9.89,;1.58,-12.55,;2.2,-13.96,;1.06,-14.99,;1.06,-16.53,;-.28,-17.3,;-1.61,-16.53,;-1.61,-14.99,;-.28,-14.22,;.04,-12.71,)|
Show InChI InChI=1S/C62H76N14O10/c1-4-65-60(85)53-20-12-26-76(53)61(86)46(19-11-25-66-62(63)64)70-54(79)47(27-35(2)3)71-57(82)50(30-38-32-67-44-17-9-6-14-41(38)44)73-55(80)48(28-36-21-23-40(78)24-22-36)72-59(84)52(34-77)75-58(83)51(31-39-33-68-45-18-10-7-15-42(39)45)74-56(81)49-29-37-13-5-8-16-43(37)69-49/h5-10,13-18,21-24,29,32-33,35,46-48,50-53,67-69,77-78H,4,11-12,19-20,25-28,30-31,34H2,1-3H3,(H,65,85)(H,70,79)(H,71,82)(H,72,84)(H,73,80)(H,74,81)(H,75,83)(H4,63,64,66)/t46-,47-,48-,50+,51+,52-,53+/m0/s1
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0.0760n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470088
PNG
(CHEMBL278704)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(OC)cc1 |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.67,(25.49,-8.55,;25.49,-10.08,;24.17,-10.86,;22.83,-10.09,;21.53,-10.86,;22.8,-8.6,;24.01,-7.71,;23.49,-6.26,;21.98,-6.26,;21.55,-7.71,;20.2,-8.47,;20.2,-10,;18.88,-7.71,;18.88,-6.16,;20.24,-5.39,;20.24,-3.86,;21.59,-3.09,;21.59,-1.56,;22.93,-.81,;20.27,-.78,;17.55,-8.45,;16.21,-7.68,;16.23,-6.13,;14.88,-8.44,;14.86,-9.96,;16.2,-10.77,;16.18,-12.3,;17.53,-10,;13.54,-7.67,;12.22,-8.42,;12.21,-9.95,;10.9,-7.64,;10.9,-6.1,;10.44,-4.65,;8.96,-4.17,;8.96,-2.62,;10.45,-2.14,;11.06,-.75,;12.6,-.59,;13.51,-1.84,;12.86,-3.25,;11.34,-3.39,;9.57,-8.41,;8.22,-7.61,;8.22,-6.09,;6.87,-8.38,;6.87,-9.92,;8.19,-10.7,;8.19,-12.25,;9.51,-13.02,;10.86,-12.27,;12.19,-13.02,;10.86,-10.73,;9.54,-9.93,;5.55,-7.6,;4.23,-8.35,;4.2,-9.9,;2.9,-7.58,;2.91,-6.05,;4.23,-5.29,;1.56,-8.34,;.23,-7.57,;.24,-6.03,;-1.12,-8.32,;-1.13,-9.87,;.2,-10.64,;1.62,-10.03,;2.64,-11.18,;1.85,-12.51,;2.32,-13.98,;1.29,-15.11,;-.21,-14.78,;-.7,-13.31,;.35,-12.19,;-2.44,-7.55,;-3.79,-8.31,;-3.77,-9.83,;-5.14,-7.57,;-6.59,-8.5,;-8.11,-7.73,;-9.55,-8.66,;-11.07,-7.89,;-11.2,-6.16,;-12.68,-5.31,;-14.16,-6.18,;-9.73,-5.23,;-8.2,-6,)|
Show InChI InChI=1S/C63H81N13O11/c1-5-66-61(85)54-17-11-29-76(54)62(86)48(16-10-28-67-63(64)65)71-56(80)49(30-37(2)3)72-59(83)52(33-41-35-69-47-15-9-7-13-45(41)47)74-57(81)50(31-39-18-23-42(78)24-19-39)73-60(84)53(36-77)75-58(82)51(32-40-34-68-46-14-8-6-12-44(40)46)70-55(79)27-22-38-20-25-43(87-4)26-21-38/h6-9,12-15,18-21,23-26,34-35,37,48-54,68-69,77-78H,5,10-11,16-17,22,27-33,36H2,1-4H3,(H,66,85)(H,70,79)(H,71,80)(H,72,83)(H,73,84)(H,74,81)(H,75,82)(H4,64,65,67)/t48-,49-,50-,51-,52+,53-,54+/m0/s1
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0.0780n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470123
PNG
(CHEMBL415643)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(O)cc1 |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.67,(27.17,-9.81,;27.19,-11.34,;25.87,-12.13,;24.53,-11.35,;23.23,-12.13,;24.5,-9.86,;25.71,-8.97,;25.2,-7.52,;23.66,-7.52,;23.24,-8.97,;21.91,-9.73,;21.89,-11.26,;20.57,-8.97,;20.59,-7.42,;21.92,-6.65,;21.94,-5.12,;23.27,-4.35,;23.29,-2.81,;24.63,-2.06,;21.95,-2.04,;19.25,-9.71,;17.91,-8.94,;17.92,-7.39,;16.57,-9.7,;16.56,-11.22,;17.89,-12.03,;17.86,-13.56,;19.21,-11.26,;15.24,-8.92,;13.9,-9.68,;13.9,-11.21,;12.58,-8.9,;12.6,-7.36,;12.13,-5.91,;10.66,-5.42,;10.66,-3.88,;12.13,-3.39,;12.76,-2.01,;14.28,-1.85,;15.19,-3.09,;14.56,-4.51,;13.03,-4.65,;11.26,-9.67,;9.9,-8.87,;9.9,-7.35,;8.57,-9.64,;8.57,-11.18,;9.89,-11.96,;11.22,-11.19,;12.57,-11.99,;12.54,-13.53,;13.86,-14.28,;11.21,-14.28,;9.87,-13.51,;7.25,-8.86,;5.91,-9.61,;5.9,-11.16,;4.59,-8.84,;4.59,-7.31,;5.93,-6.55,;3.23,-9.6,;1.91,-8.83,;1.93,-7.29,;.56,-9.58,;.56,-11.13,;1.88,-11.9,;3.3,-11.29,;4.33,-12.44,;3.54,-13.77,;4.01,-15.24,;2.97,-16.37,;1.46,-16.04,;1,-14.57,;2.04,-13.45,;-.76,-8.81,;-2.09,-9.58,;-2.08,-11.09,;-3.45,-8.83,;-4.89,-9.76,;-6.43,-8.97,;-7.86,-9.9,;-9.4,-9.13,;-9.49,-7.41,;-11.01,-6.55,;-8.04,-6.48,;-6.51,-7.26,)|
Show InChI InChI=1S/C62H79N13O11/c1-4-65-60(85)53-16-10-28-75(53)61(86)47(15-9-27-66-62(63)64)70-55(80)48(29-36(2)3)71-58(83)51(32-40-34-68-46-14-8-6-12-44(40)46)73-56(81)49(30-38-19-24-42(78)25-20-38)72-59(84)52(35-76)74-57(82)50(31-39-33-67-45-13-7-5-11-43(39)45)69-54(79)26-21-37-17-22-41(77)23-18-37/h5-8,11-14,17-20,22-25,33-34,36,47-53,67-68,76-78H,4,9-10,15-16,21,26-32,35H2,1-3H3,(H,65,85)(H,69,79)(H,70,80)(H,71,83)(H,72,84)(H,73,81)(H,74,82)(H4,63,64,66)/t47-,48-,49-,50-,51+,52-,53+/m0/s1
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0.0850n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470095
PNG
(CHEMBL216589)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(Cl)cc1)NC(=O)CCc1ccc(F)cc1 |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.76,(21.37,-6.49,;21.39,-8.02,;20.07,-8.81,;18.73,-8.03,;17.43,-8.81,;18.7,-6.54,;19.91,-5.65,;19.4,-4.2,;17.86,-4.2,;17.44,-5.65,;16.11,-6.41,;16.09,-7.94,;14.77,-5.65,;14.79,-4.1,;16.12,-3.33,;16.14,-1.8,;17.47,-1.03,;17.49,.5,;18.83,1.26,;16.15,1.28,;13.45,-6.39,;12.11,-5.62,;12.13,-4.07,;10.77,-6.38,;10.76,-7.9,;12.09,-8.71,;13.41,-7.94,;12.06,-10.25,;9.44,-5.61,;8.1,-6.36,;8.1,-7.89,;6.78,-5.58,;6.8,-4.04,;6.33,-2.59,;4.87,-2.11,;4.87,-.56,;6.33,-.08,;6.96,1.31,;8.48,1.47,;9.39,.23,;8.76,-1.19,;7.23,-1.33,;5.46,-6.35,;4.1,-5.55,;4.1,-4.03,;2.77,-6.33,;2.77,-7.86,;4.09,-8.65,;5.42,-7.87,;6.77,-8.67,;6.74,-10.21,;8.07,-10.97,;5.41,-10.97,;4.07,-10.19,;1.45,-5.54,;.11,-6.29,;.1,-7.84,;-1.21,-5.52,;-1.21,-4,;.13,-3.23,;-2.57,-6.28,;-3.89,-5.51,;-3.87,-3.97,;-5.24,-6.26,;-5.24,-7.81,;-3.92,-8.58,;-4.02,-10.13,;-2.73,-10.97,;-1.34,-10.31,;-.02,-11.08,;-1.25,-8.77,;-2.53,-7.9,;-6.56,-5.49,;-7.89,-6.25,;-7.85,-7.76,;-9.27,-5.55,;-10.69,-6.52,;-12.24,-5.8,;-13.65,-6.78,;-15.2,-6.04,;-15.36,-4.33,;-16.86,-3.52,;-13.94,-3.33,;-12.39,-4.07,)|
Show InChI InChI=1S/C60H76ClFN12O10/c1-4-65-58(83)51-12-8-28-74(51)59(84)45(11-7-27-66-60(63)64)69-53(78)46(29-35(2)3)70-56(81)49(32-39-33-67-44-10-6-5-9-43(39)44)72-55(80)48(31-38-17-24-42(76)25-18-38)71-57(82)50(34-75)73-54(79)47(30-37-13-20-40(61)21-14-37)68-52(77)26-19-36-15-22-41(62)23-16-36/h5-6,9-10,13-18,20-25,33,35,45-51,67,75-76H,4,7-8,11-12,19,26-32,34H2,1-3H3,(H,65,83)(H,68,77)(H,69,78)(H,70,81)(H,71,82)(H,72,80)(H,73,79)(H4,63,64,66)/t45-,46-,47-,48-,49+,50-,51+/m0/s1
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0.0890n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Gag-Pol polyprotein [489-587]


(Human immunodeficiency virus type 1)
BDBM50041043
PNG
((1-{(1S,2S,3R,4S)-1-Benzyl-2,3-dihydroxy-4-[3-meth...)
Show SMILES CC(C)C(NC(=O)OCc1ccccn1)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)C(NC(=O)OCc1ccccn1)C(C)C
Show InChI InChI=1S/C42H52N6O8/c1-27(2)35(47-41(53)55-25-31-19-11-13-21-43-31)39(51)45-33(23-29-15-7-5-8-16-29)37(49)38(50)34(24-30-17-9-6-10-18-30)46-40(52)36(28(3)4)48-42(54)56-26-32-20-12-14-22-44-32/h5-22,27-28,33-38,49-50H,23-26H2,1-4H3,(H,45,51)(H,46,52)(H,47,53)(H,48,54)/t33-,34-,35?,36?,37-,38+/m0/s1
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PubMed
0.0900n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibitory activity against HIV-1 protease


J Med Chem 37: 1035-54 (1994)


BindingDB Entry DOI: 10.7270/Q26Q1XWX
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50409919
PNG
(CHEMBL12282)
Show SMILES CC[C@H]1OC(=O)[C@H](C)[C@@H](OC(=O)N2[C@@H](C)COC2=O)[C@H](C)[C@@H](OC2O[C@H](C)C[C@@H]([C@H]2O)N(C)CC2CC2)[C@](C)(C[C@@H](C)C(=O)[C@H](C)[C@H]2N(CCc3ccc(F)c(Cl)c3)C(=O)O[C@]12C)OC
Show InChI InChI=1S/C47H69ClFN3O13/c1-12-35-47(9)39(51(43(56)65-47)18-17-30-15-16-33(49)32(48)20-30)27(5)36(53)24(2)21-46(8,59-11)40(64-42-37(54)34(19-26(4)61-42)50(10)22-31-13-14-31)28(6)38(29(7)41(55)62-35)63-45(58)52-25(3)23-60-44(52)57/h15-16,20,24-29,31,34-35,37-40,42,54H,12-14,17-19,21-23H2,1-11H3/t24-,25+,26-,27+,28+,29-,34+,35-,37-,38+,39-,40-,42?,46+,47-/m1/s1
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0.110n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
In vitro binding affinity to rat luteinizing hormone-releasing hormone (LHRH) receptor cloned in CHO cells


J Med Chem 47: 1085-97 (2004)

Checked by Author
Article DOI: 10.1021/jm030418i
BindingDB Entry DOI: 10.7270/Q2ZG6TF5
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470100
PNG
(CHEMBL415562)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)N(C)C(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(F)cc1 |wU:12.20,57.61,wD:45.57,31.44,23.28,5.4,64.68,(26.08,-8.88,;26.08,-10.41,;24.76,-11.2,;23.43,-10.44,;22.12,-11.2,;23.4,-8.93,;24.6,-8.05,;24.09,-6.61,;22.57,-6.61,;22.14,-8.06,;20.8,-8.8,;20.8,-10.34,;19.48,-8.05,;19.48,-6.5,;20.84,-5.74,;20.84,-4.2,;22.19,-3.44,;22.19,-1.91,;23.53,-1.14,;20.87,-1.13,;18.15,-8.8,;16.81,-8.03,;16.83,-6.48,;15.48,-8.77,;15.46,-10.31,;16.8,-11.1,;18.13,-10.31,;16.78,-12.63,;14.14,-7.99,;12.82,-8.75,;12.81,-10.28,;11.5,-7.98,;11.5,-6.45,;11.04,-4.99,;9.57,-4.51,;9.57,-2.96,;11.05,-2.49,;11.66,-1.09,;13.21,-.93,;14.11,-2.17,;13.46,-3.58,;11.94,-3.74,;10.17,-8.73,;8.83,-7.96,;8.83,-6.42,;7.48,-8.72,;7.48,-10.25,;8.8,-11.04,;10.15,-10.28,;11.47,-11.05,;11.47,-12.6,;12.79,-13.37,;10.12,-13.36,;8.8,-12.58,;6.16,-7.93,;4.84,-8.69,;4.81,-10.25,;3.51,-7.92,;3.52,-6.38,;4.84,-5.63,;2.17,-8.67,;.82,-9.44,;.84,-7.9,;.85,-6.37,;-.5,-8.66,;-.51,-10.2,;.82,-10.99,;2.23,-10.36,;3.25,-11.5,;2.46,-12.84,;2.93,-14.3,;1.9,-15.43,;.4,-15.11,;-.09,-13.65,;.97,-12.52,;-1.82,-7.9,;-3.18,-8.64,;-3.14,-10.17,;-4.53,-7.92,;-5.95,-8.86,;-7.5,-8.09,;-8.94,-9.04,;-10.46,-8.28,;-10.58,-6.57,;-12.09,-5.71,;-9.13,-5.61,;-7.6,-6.38,)|
Show InChI InChI=1S/C63H80FN13O10/c1-5-67-59(84)53-17-11-29-77(53)62(87)48(16-10-28-68-63(65)66)72-56(81)49(30-37(2)3)73-58(83)51(32-40-34-69-46-14-8-6-12-44(40)46)74-57(82)50(31-39-20-25-43(79)26-21-39)75-60(85)54(36-78)76(4)61(86)52(33-41-35-70-47-15-9-7-13-45(41)47)71-55(80)27-22-38-18-23-42(64)24-19-38/h6-9,12-15,18-21,23-26,34-35,37,48-54,69-70,78-79H,5,10-11,16-17,22,27-33,36H2,1-4H3,(H,67,84)(H,71,80)(H,72,81)(H,73,83)(H,74,82)(H,75,85)(H4,65,66,68)/t48-,49-,50-,51+,52-,53+,54-/m0/s1
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0.135n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50041045
PNG
((4S,6S)-4-Ethylamino-7,7-dioxo-6-propyl-4,5,6,7-te...)
Show SMILES CCC[C@H]1C[C@H](NCC)c2cc(sc2S1(=O)=O)S(N)(=O)=O
Show InChI InChI=1S/C12H20N2O4S3/c1-3-5-8-6-10(14-4-2)9-7-11(21(13,17)18)19-12(9)20(8,15)16/h7-8,10,14H,3-6H2,1-2H3,(H2,13,17,18)/t8-,10-/m0/s1
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0.140n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibitory constant towards Human Carbonic anhydrase II (HCA II)


J Med Chem 37: 1035-54 (1994)


BindingDB Entry DOI: 10.7270/Q26Q1XWX
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Gag-Pol polyprotein [489-587]


(Human immunodeficiency virus type 1)
BDBM197
PNG
((2S)-N-[(2S,3R,4R,5S)-3,4-dihydroxy-5-[(2S)-3-meth...)
Show SMILES CC(C)[C@H](NC(=O)N(C)Cc1ccccn1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)N(C)Cc1ccccn1)C(C)C |r|
Show InChI InChI=1S/C44H58N8O6/c1-29(2)37(49-43(57)51(5)27-33-21-13-15-23-45-33)41(55)47-35(25-31-17-9-7-10-18-31)39(53)40(54)36(26-32-19-11-8-12-20-32)48-42(56)38(30(3)4)50-44(58)52(6)28-34-22-14-16-24-46-34/h7-24,29-30,35-40,53-54H,25-28H2,1-6H3,(H,47,55)(H,48,56)(H,49,57)(H,50,58)/t35-,36-,37-,38-,39+,40+/m0/s1
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0.150n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibitory activity against HIV-1 protease


J Med Chem 37: 1035-54 (1994)


BindingDB Entry DOI: 10.7270/Q26Q1XWX
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Gag-Pol polyprotein [489-587]


(Human immunodeficiency virus type 1)
BDBM50041023
PNG
((1-{(1S,2S,3S,4S)-1-Benzyl-2,3-dihydroxy-4-[3-meth...)
Show SMILES CC(C)C(NC(=O)OCc1ccccn1)C(=O)N[C@@H](Cc1ccccc1)[C@H](O)[C@@H](O)[C@H](Cc1ccccc1)NC(=O)C(NC(=O)OCc1ccccn1)C(C)C
Show InChI InChI=1S/C42H52N6O8/c1-27(2)35(47-41(53)55-25-31-19-11-13-21-43-31)39(51)45-33(23-29-15-7-5-8-16-29)37(49)38(50)34(24-30-17-9-6-10-18-30)46-40(52)36(28(3)4)48-42(54)56-26-32-20-12-14-22-44-32/h5-22,27-28,33-38,49-50H,23-26H2,1-4H3,(H,45,51)(H,46,52)(H,47,53)(H,48,54)/t33-,34-,35?,36?,37-,38-/m0/s1
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0.160n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibitory activity against HIV-1 protease


J Med Chem 37: 1035-54 (1994)


BindingDB Entry DOI: 10.7270/Q26Q1XWX
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470126
PNG
(CHEMBL266032)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccccc1)NC(C)=O |wU:57.63,12.20,77.91,wD:45.57,31.44,63.79,23.28,5.4,(17.4,.92,;17.4,-.62,;16.08,-1.39,;14.73,-.64,;13.42,-1.39,;14.7,.87,;15.92,1.76,;15.41,3.21,;13.87,3.21,;13.44,1.75,;12.1,.99,;12.09,-.55,;10.78,1.76,;10.79,3.33,;12.12,4.07,;12.14,5.61,;13.48,6.4,;13.48,7.92,;14.83,8.68,;12.16,8.71,;9.44,1.02,;8.09,1.79,;8.12,3.34,;6.75,1.03,;6.75,-.51,;8.08,-1.29,;9.41,-.52,;8.06,-2.83,;5.42,1.82,;4.08,1.05,;4.07,-.49,;2.76,1.83,;2.77,3.37,;2.29,4.83,;.83,5.31,;.83,6.86,;2.31,7.33,;2.93,8.75,;4.47,8.91,;5.37,7.66,;4.75,6.24,;3.21,6.08,;1.42,1.06,;.07,1.85,;.07,3.39,;-1.27,1.08,;-1.27,-.46,;.06,-1.23,;.04,-2.79,;1.38,-3.57,;2.73,-2.8,;4.05,-3.57,;2.74,-1.26,;1.39,-.48,;-2.59,1.88,;-3.93,1.11,;-3.95,-.45,;-5.26,1.89,;-5.25,3.42,;-3.91,4.19,;-6.61,1.12,;-7.94,1.91,;-7.92,3.45,;-9.29,1.14,;-9.29,-.4,;-7.98,-1.19,;-6.54,-.56,;-5.52,-1.71,;-6.31,-3.05,;-5.84,-4.52,;-6.89,-5.66,;-8.39,-5.34,;-8.85,-3.86,;-7.82,-2.73,;-10.61,1.91,;-11.95,1.15,;-11.99,-.38,;-13.28,1.95,;-13.27,3.49,;-11.92,4.26,;-11.95,5.8,;-10.57,6.54,;-9.26,5.77,;-9.26,4.23,;-10.61,3.46,;-14.62,1.18,;-15.82,2.14,;-17.24,1.56,;-15.6,3.65,)|
Show InChI InChI=1S/C64H82N14O11/c1-5-67-62(88)55-22-14-28-78(55)63(89)48(21-13-27-68-64(65)66)72-56(82)49(29-37(2)3)73-59(85)52(32-41-34-69-46-19-11-9-17-44(41)46)76-58(84)51(31-40-23-25-43(81)26-24-40)74-61(87)54(36-79)77-60(86)53(33-42-35-70-47-20-12-10-18-45(42)47)75-57(83)50(71-38(4)80)30-39-15-7-6-8-16-39/h6-12,15-20,23-26,34-35,37,48-55,69-70,79,81H,5,13-14,21-22,27-33,36H2,1-4H3,(H,67,88)(H,71,80)(H,72,82)(H,73,85)(H,74,87)(H,75,83)(H,76,84)(H,77,86)(H4,65,66,68)/t48-,49-,50-,51-,52+,53-,54-,55+/m0/s1
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0.166n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Carbonic anhydrase 2


(Homo sapiens (Human))
BDBM50041037
PNG
((4S,6R)-4-Ethylamino-7,7-dioxo-6-propyl-4,5,6,7-te...)
Show SMILES CCC[C@@H]1C[C@H](NCC)c2cc(sc2S1(=O)=O)S(N)(=O)=O
Show InChI InChI=1S/C12H20N2O4S3/c1-3-5-8-6-10(14-4-2)9-7-11(21(13,17)18)19-12(9)20(8,15)16/h7-8,10,14H,3-6H2,1-2H3,(H2,13,17,18)/t8-,10+/m1/s1
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0.170n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibitory constant towards Human Carbonic anhydrase II (HCA II)


J Med Chem 37: 1035-54 (1994)


BindingDB Entry DOI: 10.7270/Q26Q1XWX
More data for this
Ligand-Target Pair
3D
3D Structure (docked)
Gag-Pol polyprotein [489-587]


(Human immunodeficiency virus type 1)
BDBM50041035
PNG
(CHEMBL269401 | N-{(1S,2R,3R,4S)-1-Benzyl-2,3-dihyd...)
Show SMILES CC(C)C(NC(=O)N(C)Cc1ccccn1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)C(NC(=O)N(C)Cc1ccccn1)C(C)C
Show InChI InChI=1S/C44H58N8O6/c1-29(2)37(49-43(57)51(5)27-33-21-13-15-23-45-33)41(55)47-35(25-31-17-9-7-10-18-31)39(53)40(54)36(26-32-19-11-8-12-20-32)48-42(56)38(30(3)4)50-44(58)52(6)28-34-22-14-16-24-46-34/h7-24,29-30,35-40,53-54H,25-28H2,1-6H3,(H,47,55)(H,48,56)(H,49,57)(H,50,58)/t35-,36-,37?,38?,39+,40+/m0/s1
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0.180n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibitory activity against HIV-1 protease


J Med Chem 37: 1035-54 (1994)


BindingDB Entry DOI: 10.7270/Q26Q1XWX
More data for this
Ligand-Target Pair
Gag-Pol polyprotein [489-587]


(Human immunodeficiency virus type 1)
BDBM50041032
PNG
((1-{(1S,2R,3R,4S)-1-Benzyl-2,3-dihydroxy-4-[3-meth...)
Show SMILES CC(C)C(NC(=O)OCc1ccccn1)C(=O)N[C@@H](Cc1ccccc1)[C@@H](O)[C@H](O)[C@H](Cc1ccccc1)NC(=O)C(NC(=O)OCc1ccccn1)C(C)C
Show InChI InChI=1S/C42H52N6O8/c1-27(2)35(47-41(53)55-25-31-19-11-13-21-43-31)39(51)45-33(23-29-15-7-5-8-16-29)37(49)38(50)34(24-30-17-9-6-10-18-30)46-40(52)36(28(3)4)48-42(54)56-26-32-20-12-14-22-44-32/h5-22,27-28,33-38,49-50H,23-26H2,1-4H3,(H,45,51)(H,46,52)(H,47,53)(H,48,54)/t33-,34-,35?,36?,37+,38+/m0/s1
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0.190n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Compound was evaluated for the inhibitory activity against HIV-1 protease


J Med Chem 37: 1035-54 (1994)


BindingDB Entry DOI: 10.7270/Q26Q1XWX
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50409920
PNG
(CHEMBL273440)
Show SMILES CC[C@H]1OC(=O)[C@H](C)[C@@H](OC(=O)N2[C@@H](C)COC2=O)[C@H](C)[C@@H](OC2O[C@H](C)C[C@@H]([C@H]2O)N(C)C(C)C)[C@](C)(C[C@@H](C)C(=O)[C@H](C)[C@H]2N(CCc3ccc(Cl)c(Cl)c3)C(=O)O[C@]12C)OC
Show InChI InChI=1S/C46H69Cl2N3O13/c1-14-34-46(11)38(50(42(55)64-46)18-17-30-15-16-31(47)32(48)20-30)27(7)35(52)24(4)21-45(10,58-13)39(63-41-36(53)33(19-26(6)60-41)49(12)23(2)3)28(8)37(29(9)40(54)61-34)62-44(57)51-25(5)22-59-43(51)56/h15-16,20,23-29,33-34,36-39,41,53H,14,17-19,21-22H2,1-13H3/t24-,25+,26-,27+,28+,29-,33+,34-,36-,37+,38-,39-,41?,45+,46-/m1/s1
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0.230n/an/an/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
In vitro binding affinity to rat luteinizing hormone-releasing hormone (LHRH) receptor cloned in CHO cells


J Med Chem 47: 1085-97 (2004)

Checked by Author
Article DOI: 10.1021/jm030418i
BindingDB Entry DOI: 10.7270/Q2ZG6TF5
More data for this
Ligand-Target Pair
Gonadotropin-releasing hormone receptor


(Rattus norvegicus)
BDBM50470090
PNG
(CHEMBL263315)
Show SMILES CCNC(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CCc1ccc(cc1)C(F)(F)F |wU:57.63,12.20,wD:45.57,31.44,23.28,5.4,63.67,(25.27,-10.18,;25.29,-11.71,;23.97,-12.5,;22.63,-11.72,;21.33,-12.5,;22.6,-10.23,;23.81,-9.34,;23.3,-7.89,;21.76,-7.92,;21.34,-9.34,;20.01,-10.1,;19.99,-11.63,;18.67,-9.34,;18.69,-7.8,;20.02,-7.03,;20.05,-5.5,;21.38,-4.73,;21.4,-3.2,;22.73,-2.45,;20.06,-2.42,;17.35,-10.08,;16.02,-9.31,;16.03,-7.77,;14.68,-10.07,;14.67,-11.59,;16,-12.4,;15.97,-13.93,;17.32,-11.63,;13.35,-9.3,;12.01,-10.05,;12.01,-11.58,;10.69,-9.28,;10.71,-7.73,;10.24,-6.29,;8.78,-5.8,;8.78,-4.26,;10.24,-3.78,;10.88,-2.39,;12.4,-2.23,;13.3,-3.48,;12.68,-4.89,;11.14,-5.03,;9.36,-10.04,;8.02,-9.25,;8.02,-7.72,;6.69,-10.02,;6.67,-11.55,;8.01,-12.33,;7.99,-13.88,;9.33,-14.65,;10.66,-13.9,;11.98,-14.65,;10.68,-12.36,;9.34,-11.56,;5.37,-9.23,;4.03,-9.99,;4.02,-11.53,;2.71,-9.21,;2.71,-7.69,;4.05,-6.93,;1.36,-9.97,;.04,-9.2,;.06,-7.67,;-1.31,-9.95,;-1.31,-11.5,;.01,-12.27,;1.43,-11.66,;2.46,-12.81,;1.67,-14.14,;2.13,-15.61,;1.1,-16.73,;-.41,-16.41,;-.87,-14.94,;.17,-13.81,;-2.63,-9.18,;-3.96,-9.94,;-3.95,-11.47,;-5.33,-9.21,;-6.75,-10.15,;-8.29,-9.37,;-8.39,-7.67,;-9.93,-6.9,;-11.36,-7.85,;-11.25,-9.57,;-9.72,-10.34,;-12.92,-7.09,;-14.57,-7.83,;-14.31,-6.38,;-13.31,-5.32,)|
Show InChI InChI=1S/C63H78F3N13O10/c1-4-69-60(88)53-16-10-28-79(53)61(89)47(15-9-27-70-62(67)68)74-55(83)48(29-36(2)3)75-58(86)51(32-40-34-72-46-14-8-6-12-44(40)46)77-56(84)49(30-38-19-24-42(81)25-20-38)76-59(87)52(35-80)78-57(85)50(31-39-33-71-45-13-7-5-11-43(39)45)73-54(82)26-21-37-17-22-41(23-18-37)63(64,65)66/h5-8,11-14,17-20,22-25,33-34,36,47-53,71-72,80-81H,4,9-10,15-16,21,26-32,35H2,1-3H3,(H,69,88)(H,73,82)(H,74,83)(H,75,86)(H,76,87)(H,77,84)(H,78,85)(H4,67,68,70)/t47-,48-,49-,50-,51+,52-,53+/m0/s1
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0.275n/an/an/an/an/an/an/an/a



TAP Pharmaceuticals, Inc.

Curated by ChEMBL


Assay Description
Inhibition of the in vitro binding of [125I]-labeled leuprolide to the rat pituitary luteinizing hormone releasing hormone (LHRH) receptor.


J Med Chem 37: 701-5 (1994)


Article DOI: 10.1021/jm00031a021
BindingDB Entry DOI: 10.7270/Q2MG7S7B
More data for this
Ligand-Target Pair
Lutropin-choriogonadotropic hormone receptor


(Rattus norvegicus)
BDBM50405770
PNG
(CHEMBL216617)
Show SMILES CCNC(=O)C1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)CCc1cccc2ccccc12
Show InChI InChI=1S/C57H72N10O9/c1-4-60-55(75)49-19-11-29-67(49)56(76)44(18-10-28-61-57(58)59)63-51(71)45(30-35(2)3)64-53(73)47(33-37-20-23-38-12-5-6-14-41(38)31-37)65-52(72)46(32-36-21-25-42(69)26-22-36)66-54(74)48(34-68)62-50(70)27-24-40-16-9-15-39-13-7-8-17-43(39)40/h5-9,12-17,20-23,25-26,31,35,44-49,68-69H,4,10-11,18-19,24,27-30,32-34H2,1-3H3,(H,60,75)(H,62,70)(H,63,71)(H,64,73)(H,65,72)(H,66,74)(H4,58,59,61)/t44-,45-,46-,47+,48-,49?/m0/s1
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PubMed
0.282n/an/an/an/an/an/an/an/a



Abbott Laboratory

Curated by ChEMBL


Assay Description
In vitro binding affinity for Luteinizing hormone releasing hormone receptor from rat pituitary cells, expressed as negative logarithm of the equilib...


J Med Chem 32: 2340-4 (1989)


BindingDB Entry DOI: 10.7270/Q2H70H1B
More data for this
Ligand-Target Pair
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