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Compile Data Set for Download or QSAR

Found 919 hits with Last Name = 'jenck' and Initial = 'f'   
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
Nociceptin receptor


(RAT)		BDBM50087691
PNG
(8-(4-Isopropyl-cyclohexyl)-1-phenyl-1,3,8-triaza-s...)
Show SMILES CC(C)[C@H]1CC[C@H](CC1)N1CCC2(CC1)N(CNC2=O)c1ccccc1 |wU:6.9,3.2,(2.69,-2.68,;3.46,-4.01,;2.69,-5.35,;5,-4.02,;5.77,-2.69,;7.31,-2.69,;8.06,-4.02,;7.31,-5.35,;5.77,-5.35,;9.6,-4.02,;10.37,-2.68,;11.91,-2.67,;12.68,-4.01,;11.91,-5.34,;10.37,-5.34,;13.56,-5.26,;15.03,-4.79,;15.03,-3.25,;13.59,-2.76,;13.1,-1.31,;13.1,-6.7,;11.58,-7.03,;11.11,-8.49,;12.14,-9.64,;13.66,-9.32,;14.12,-7.85,)|
Show InChI InChI=1S/C22H33N3O/c1-17(2)18-8-10-19(11-9-18)24-14-12-22(13-15-24)21(26)23-16-25(22)20-6-4-3-5-7-20/h3-7,17-19H,8-16H2,1-2H3,(H,23,26)/t18-,19+
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 0.0790n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [leucyl-3H]-OFQ to membrane of human embryonic kidney 293 cells overexpressing rat Opioid receptor like 1

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Nociceptin receptor


(RAT)		BDBM50087692
PNG
(8-Cyclodecyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCCCC1
Show InChI InChI=1S/C23H35N3O/c27-22-23(26(19-24-22)21-13-9-6-10-14-21)15-17-25(18-16-23)20-11-7-4-2-1-3-5-8-12-20/h6,9-10,13-14,20H,1-5,7-8,11-12,15-19H2,(H,24,27)
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 0.0820n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [leucyl-3H]-OFQ to membrane of human embryonic kidney 293 cells overexpressing rat Opioid receptor like 1

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))		BDBM50027473
PNG
(3-Methyl-1-phenethyl-4-(phenyl-propionyl-amino)-pi...)
Show SMILES CCC(=O)N(c1ccccc1)[C@]1(CCN(CCc2ccccc2)C[C@H]1C)C(=O)OC
Show InChI InChI=1S/C25H32N2O3/c1-4-23(28)27(22-13-9-6-10-14-22)25(24(29)30-3)16-18-26(19-20(25)2)17-15-21-11-7-5-8-12-21/h5-14,20H,4,15-19H2,1-3H3/t20-,25+/m1/s1
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 0.140n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Competitive binding displacement analyses was performed from permanently transfected HEK293 cells expressing Opioid receptor mu 1

J Med Chem 43: 1329-38 (2001)


BindingDB Entry DOI: 10.7270/Q2ZG6SZG
More data for this
Ligand-Target Pair		3D
3D Structure (crystal)
Delta-type opioid receptor


(Rattus norvegicus (rat))		BDBM50057010
PNG
((S)-4-((S)-2-{(R)-2-[(S)-2-Amino-3-(4-hydroxy-phen...)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)[C@@H](C)CC)C(=O)NCC(N)=O
Show InChI InChI=1S/C40H58N8O10/c1-6-22(3)33(39(57)43-21-31(42)50)48-40(58)34(23(4)7-2)47-37(55)29(17-18-32(51)52)45-38(56)30(20-25-11-9-8-10-12-25)46-35(53)24(5)44-36(54)28(41)19-26-13-15-27(49)16-14-26/h8-16,22-24,28-30,33-34,49H,6-7,17-21,41H2,1-5H3,(H2,42,50)(H,43,57)(H,44,54)(H,45,56)(H,46,53)(H,47,55)(H,48,58)(H,51,52)/t22-,23-,24+,28-,29-,30-,33-,34-/m0/s1
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 0.190n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [Ile5,6-3H]-deltorphin to membrane from baby hamster kidney cells infected with forest virus encoding the ...

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Rattus norvegicus (rat))		BDBM50087697
PNG
(8-Cycloundecyl-1-phenyl-1,3,8-triaza-spiro[4.5]dec...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCCCCC1
Show InChI InChI=1S/C24H37N3O/c28-23-24(27(20-25-23)22-14-10-7-11-15-22)16-18-26(19-17-24)21-12-8-5-3-1-2-4-6-9-13-21/h7,10-11,14-15,21H,1-6,8-9,12-13,16-20H2,(H,25,28)
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 0.210n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [N-allyl-2-3-3H]-naloxone to membrane of baby hamster kidney cells infected with forest virus encoding the...

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Nociceptin receptor


(RAT)		BDBM50087687
PNG
(8-Cyclononyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCCC1
Show InChI InChI=1S/C22H33N3O/c26-21-22(25(18-23-21)20-12-8-5-9-13-20)14-16-24(17-15-22)19-10-6-3-1-2-4-7-11-19/h5,8-9,12-13,19H,1-4,6-7,10-11,14-18H2,(H,23,26)
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 0.240n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [leucyl-3H]-OFQ to membrane of human embryonic kidney 293 cells overexpressing rat Opioid receptor like 1

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Rattus norvegicus (rat))		BDBM50087685
PNG
(8-Cyclododecyl-1-phenyl-1,3,8-triaza-spiro[4.5]dec...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCCCCCC1
Show InChI InChI=1S/C25H39N3O/c29-24-25(28(21-26-24)23-15-11-8-12-16-23)17-19-27(20-18-25)22-13-9-6-4-2-1-3-5-7-10-14-22/h8,11-12,15-16,22H,1-7,9-10,13-14,17-21H2,(H,26,29)
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 0.280n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [N-allyl-2-3-3H]-naloxone to membrane of baby hamster kidney cells infected with forest virus encoding the...

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Homo sapiens (Human))		BDBM50471324
PNG
(CHEMBL318639)
Show SMILES COc1ccc2c(c1)-c1c(ccn1CC(C)N)C2(C)C
Show InChI InChI=1S/C17H22N2O/c1-11(18)10-19-8-7-15-16(19)13-9-12(20-4)5-6-14(13)17(15,2)3/h5-9,11H,10,18H2,1-4H3
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 0.398n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Inc

Curated by ChEMBL


Assay Description
Binding affinity against human 5-hydroxytryptamine 2C receptor using displacement of [3H]DOB

J Med Chem 40: 2762-9 (1997)


Article DOI: 10.1021/jm970030l
BindingDB Entry DOI: 10.7270/Q270845Q
More data for this
Ligand-Target Pair
Nociceptin receptor


(RAT)		BDBM50087698
PNG
(8-(R)-Acenaphthen-1-yl-1-phenyl-1,3,8-triaza-spiro...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)[C@@H]1Cc2cccc3cccc1c23
Show InChI InChI=1S/C25H25N3O/c29-24-25(28(17-26-24)20-9-2-1-3-10-20)12-14-27(15-13-25)22-16-19-8-4-6-18-7-5-11-21(22)23(18)19/h1-11,22H,12-17H2,(H,26,29)/t22-/m1/s1
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 0.410n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [leucyl-3H]-OFQ to membrane of human embryonic kidney 293 cells overexpressing rat Opioid receptor like 1

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474329
PNG
(CHEMBL315551)
Show SMILES [H][C@]12CN(C)C[C@@]1([H])C1(CCN(CC1)C1CCCCCCCCC1)N(C2)c1ccccc1
Show InChI InChI=1S/C27H43N3/c1-28-20-23-21-30(25-14-10-7-11-15-25)27(26(23)22-28)16-18-29(19-17-27)24-12-8-5-3-2-4-6-9-13-24/h7,10-11,14-15,23-24,26H,2-6,8-9,12-13,16-22H2,1H3/t23-,26-/m1/s1
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 0.447n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
Nociceptin receptor


(RAT)		BDBM50087697
PNG
(8-Cycloundecyl-1-phenyl-1,3,8-triaza-spiro[4.5]dec...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCCCCC1
Show InChI InChI=1S/C24H37N3O/c28-23-24(27(20-25-23)22-14-10-7-11-15-22)16-18-26(19-17-24)21-12-8-5-3-1-2-4-6-9-13-21/h7,10-11,14-15,21H,1-6,8-9,12-13,16-20H2,(H,25,28)
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 0.490n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [leucyl-3H]-OFQ to membrane of human embryonic kidney 293 cells overexpressing rat Opioid receptor like 1

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50087016
PNG
(8-Acenaphthen-1-yl-1-phenyl-1,3,8-triaza-spiro[4.5...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1Cc2cccc3cccc1c23
Show InChI InChI=1S/C25H25N3O/c29-24-25(28(17-26-24)20-9-2-1-3-10-20)12-14-27(15-13-25)22-16-19-8-4-6-18-7-5-11-21(22)23(18)19/h1-11,22H,12-17H2,(H,26,29)
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 0.520n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Competitive binding affinity against transfected HEK293 cells expressing human Opioid receptor like 1

J Med Chem 43: 1329-38 (2001)


BindingDB Entry DOI: 10.7270/Q2ZG6SZG
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474331
PNG
(CHEMBL316086)
Show SMILES [H][C@]12CN(C)C[C@@]1([H])C1(CCN(CC1)[C@H]1CC[C@]3([H])CCCC[C@]3([H])C1)N(C2)c1ccccc1
Show InChI InChI=1S/C27H41N3/c1-28-18-23-19-30(24-9-3-2-4-10-24)27(26(23)20-28)13-15-29(16-14-27)25-12-11-21-7-5-6-8-22(21)17-25/h2-4,9-10,21-23,25-26H,5-8,11-20H2,1H3/t21-,22+,23+,25-,26+/m0/s1
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 0.525n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474328
PNG
(CHEMBL330291)
Show SMILES [H][C@]12CN(C)C[C@@]1([H])C1(CCN(CC1)C1CCCCCCCC1)N(C2)c1ccccc1
Show InChI InChI=1S/C26H41N3/c1-27-19-22-20-29(24-13-9-6-10-14-24)26(25(22)21-27)15-17-28(18-16-26)23-11-7-4-2-3-5-8-12-23/h6,9-10,13-14,22-23,25H,2-5,7-8,11-12,15-21H2,1H3/t22-,25-/m1/s1
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 0.646n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Rattus norvegicus (rat))		BDBM50087692
PNG
(8-Cyclodecyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCCCC1
Show InChI InChI=1S/C23H35N3O/c27-22-23(26(19-24-22)21-13-9-6-10-14-21)15-17-25(18-16-23)20-11-7-4-2-1-3-5-8-12-20/h6,9-10,13-14,20H,1-5,7-8,11-12,15-19H2,(H,24,27)
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 0.660n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [N-allyl-2-3-3H]-naloxone to membrane of baby hamster kidney cells infected with forest virus encoding the...

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474330
PNG
(CHEMBL2112342)
Show SMILES [H][C@]12CN(CCCC)C[C@@]1([H])C1(CCN(CC1)[C@@H]1CC[C@@H](CC1)C(C)C)N(C2)c1ccccc1 |wU:17.18,20.25,1.0,9.10,(8.36,-6.3,;7.25,-5.22,;8.5,-4.32,;8.04,-2.86,;8.95,-1.61,;10.48,-1.78,;11.39,-.54,;12.91,-.71,;6.5,-2.85,;6.01,-4.32,;4.98,-3.18,;4.76,-5.22,;4.13,-6.62,;2.61,-6.79,;1.7,-5.54,;2.33,-4.13,;3.85,-3.97,;.17,-5.71,;-.74,-4.46,;-2.27,-4.62,;-2.9,-6.02,;-2,-7.27,;-.46,-7.11,;-4.44,-6.18,;-5.07,-7.58,;-5.33,-4.92,;5.25,-6.69,;6.79,-6.69,;4.4,-7.97,;2.86,-7.88,;2.01,-9.16,;2.7,-10.55,;4.24,-10.64,;5.09,-9.35,)|
Show InChI InChI=1S/C29H47N3/c1-4-5-17-30-20-25-21-32(27-9-7-6-8-10-27)29(28(25)22-30)15-18-31(19-16-29)26-13-11-24(12-14-26)23(2)3/h6-10,23-26,28H,4-5,11-22H2,1-3H3/t24-,25-,26+,28-/m1/s1
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 0.661n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50087008
PNG
(8-indan-1-yl-1-phenyl-1,3,8-triaza-spiro[4.5]decan...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCc2ccccc12
Show InChI InChI=1S/C22H25N3O/c26-21-22(25(16-23-21)18-7-2-1-3-8-18)12-14-24(15-13-22)20-11-10-17-6-4-5-9-19(17)20/h1-9,20H,10-16H2,(H,23,26)
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 0.700n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Competitive binding affinity against transfected HEK293 cells expressing Opioid receptor like 1

J Med Chem 43: 1329-38 (2001)


BindingDB Entry DOI: 10.7270/Q2ZG6SZG
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474321
PNG
(CHEMBL2112348)
Show SMILES [H][C@]12CN(CCO)C[C@@]1([H])C1(CCN(CC1)[C@@H]1CC[C@@H](CC1)C(C)C)N(C2)c1ccccc1 |wU:16.17,19.24,8.9,1.0,(13.25,-6.15,;12.15,-5.08,;13.39,-4.17,;12.92,-2.72,;13.84,-1.47,;15.36,-1.64,;16.27,-.4,;11.39,-2.71,;10.9,-4.17,;9.87,-3.03,;9.66,-5.08,;9.04,-6.48,;7.5,-6.64,;6.59,-5.4,;7.22,-3.99,;8.76,-3.82,;5.07,-5.56,;4.16,-4.31,;2.64,-4.47,;2.01,-5.87,;2.92,-7.13,;4.43,-6.96,;.47,-6.03,;-.16,-7.45,;-.43,-4.78,;10.14,-6.55,;11.68,-6.55,;9.29,-7.83,;9.99,-9.2,;9.13,-10.49,;7.59,-10.4,;6.92,-9.01,;7.76,-7.73,)|
Show InChI InChI=1S/C27H43N3O/c1-21(2)22-8-10-24(11-9-22)29-14-12-27(13-15-29)26-20-28(16-17-31)18-23(26)19-30(27)25-6-4-3-5-7-25/h3-7,21-24,26,31H,8-20H2,1-2H3/t22-,23-,24+,26-/m1/s1
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 0.776n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Rattus norvegicus (rat))		BDBM50087697
PNG
(8-Cycloundecyl-1-phenyl-1,3,8-triaza-spiro[4.5]dec...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCCCCC1
Show InChI InChI=1S/C24H37N3O/c28-23-24(27(20-25-23)22-14-10-7-11-15-22)16-18-26(19-17-24)21-12-8-5-3-1-2-4-6-9-13-21/h7,10-11,14-15,21H,1-6,8-9,12-13,16-20H2,(H,25,28)
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 0.820n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [N-allyl-2-3-3H]-naloxone to membrane of baby hamster kidney cells infected with forest virus encoding the...

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Nociceptin receptor


(RAT)		BDBM50087685
PNG
(8-Cyclododecyl-1-phenyl-1,3,8-triaza-spiro[4.5]dec...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCCCCCC1
Show InChI InChI=1S/C25H39N3O/c29-24-25(28(21-26-24)23-15-11-8-12-16-23)17-19-27(20-18-25)22-13-9-6-4-2-1-3-5-7-10-14-22/h8,11-12,15-16,22H,1-7,9-10,13-14,17-21H2,(H,26,29)
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 0.950n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [leucyl-3H]-OFQ to membrane of human embryonic kidney 293 cells overexpressing rat Opioid receptor like 1

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Homo sapiens (Human))		BDBM50108306
PNG
((S)-1-(5,6-difluoro-1H-indol-1-yl)propan-2-amine |...)
Show SMILES C[C@H](N)Cn1ccc2cc(F)c(F)cc12
Show InChI InChI=1S/C11H12F2N2/c1-7(14)6-15-3-2-8-4-9(12)10(13)5-11(8)15/h2-5,7H,6,14H2,1H3/t7-/m0/s1
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 1n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Inc

Curated by ChEMBL


Assay Description
Binding affinity against human 5-hydroxytryptamine 2C receptor using displacement of [3H]DOB

J Med Chem 40: 2762-9 (1997)


Article DOI: 10.1021/jm970030l
BindingDB Entry DOI: 10.7270/Q270845Q
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Homo sapiens (Human))		BDBM50471326
PNG
(CHEMBL2114265)
Show SMILES COc1ccc2Cc3ccn(C[C@H](C)N)c3-c2c1 |r|
Show InChI InChI=1S/C15H18N2O/c1-10(16)9-17-6-5-12-7-11-3-4-13(18-2)8-14(11)15(12)17/h3-6,8,10H,7,9,16H2,1-2H3/t10-/m0/s1
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 1n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Inc

Curated by ChEMBL


Assay Description
Binding affinity against human 5-hydroxytryptamine 2C receptor using displacement of [3H]DOB

J Med Chem 40: 2762-9 (1997)


Article DOI: 10.1021/jm970030l
BindingDB Entry DOI: 10.7270/Q270845Q
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Homo sapiens (Human))		BDBM50471314
PNG
(CHEMBL414163)
Show SMILES COc1ccc2Cc3ccn(CC(C)N)c3-c2c1
Show InChI InChI=1S/C15H18N2O/c1-10(16)9-17-6-5-12-7-11-3-4-13(18-2)8-14(11)15(12)17/h3-6,8,10H,7,9,16H2,1-2H3
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 1n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Inc

Curated by ChEMBL


Assay Description
Binding affinity against human 5-hydroxytryptamine 2C receptor using displacement of [3H]DOB

J Med Chem 40: 2762-9 (1997)


Article DOI: 10.1021/jm970030l
BindingDB Entry DOI: 10.7270/Q270845Q
More data for this
Ligand-Target Pair
Orexin receptor type 2


(Homo sapiens (Human))		BDBM50232703
PNG
((S)-1-(2-(1H-benzo[d]imidazol-2-ylthio)acetyl)-N-(...)
Show SMILES O=C(CSc1nc2ccccc2[nH]1)N1CCC[C@H]1C(=O)Nc1ccccc1-n1cccc1 |r|
Show InChI InChI=1S/C24H23N5O2S/c30-22(16-32-24-26-17-8-1-2-9-18(17)27-24)29-15-7-12-21(29)23(31)25-19-10-3-4-11-20(19)28-13-5-6-14-28/h1-6,8-11,13-14,21H,7,12,15-16H2,(H,25,31)(H,26,27)/t21-/m0/s1
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 1n/an/an/an/an/an/an/an/a



Actelion Pharmaceuticals Ltd.

Curated by ChEMBL


Assay Description
Antagonist activity at human OX2 receptor

J Med Chem 52: 891-903 (2009)


Article DOI: 10.1021/jm801296d
BindingDB Entry DOI: 10.7270/Q2TM7B3D
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474322
PNG
(CHEMBL2112345)
Show SMILES [H][C@]12CN(C)C[C@@]1([H])C1(CCN(CC1)[C@@H]1CC[C@@H](CC1)C(C)C)N(C2)c1ccccc1 |wU:14.15,17.22,6.7,1.0,(17.01,-3.4,;15.89,-2.33,;17.15,-1.42,;16.68,.04,;17.59,1.28,;15.15,.05,;14.66,-1.42,;13.63,-.28,;13.4,-2.33,;12.77,-3.73,;11.26,-3.89,;10.35,-2.64,;10.98,-1.23,;12.49,-1.07,;8.81,-2.8,;7.9,-1.56,;6.37,-1.72,;5.74,-3.12,;6.65,-4.38,;8.18,-4.22,;4.2,-3.28,;3.57,-4.69,;3.32,-2.03,;13.89,-3.8,;15.43,-3.8,;13.05,-5.08,;13.73,-6.45,;12.89,-7.74,;11.35,-7.65,;10.65,-6.27,;11.51,-4.98,)|
Show InChI InChI=1S/C26H41N3/c1-20(2)21-9-11-23(12-10-21)28-15-13-26(14-16-28)25-19-27(3)17-22(25)18-29(26)24-7-5-4-6-8-24/h4-8,20-23,25H,9-19H2,1-3H3/t21-,22-,23+,25-/m1/s1
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 1.20n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474322
PNG
(CHEMBL2112345)
Show SMILES [H][C@]12CN(C)C[C@@]1([H])C1(CCN(CC1)[C@@H]1CC[C@@H](CC1)C(C)C)N(C2)c1ccccc1 |wU:14.15,17.22,6.7,1.0,(17.01,-3.4,;15.89,-2.33,;17.15,-1.42,;16.68,.04,;17.59,1.28,;15.15,.05,;14.66,-1.42,;13.63,-.28,;13.4,-2.33,;12.77,-3.73,;11.26,-3.89,;10.35,-2.64,;10.98,-1.23,;12.49,-1.07,;8.81,-2.8,;7.9,-1.56,;6.37,-1.72,;5.74,-3.12,;6.65,-4.38,;8.18,-4.22,;4.2,-3.28,;3.57,-4.69,;3.32,-2.03,;13.89,-3.8,;15.43,-3.8,;13.05,-5.08,;13.73,-6.45,;12.89,-7.74,;11.35,-7.65,;10.65,-6.27,;11.51,-4.98,)|
Show InChI InChI=1S/C26H41N3/c1-20(2)21-9-11-23(12-10-21)28-15-13-26(14-16-28)25-19-27(3)17-22(25)18-29(26)24-7-5-4-6-8-24/h4-8,20-23,25H,9-19H2,1-3H3/t21-,22-,23+,25-/m1/s1
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 1.20n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Homo sapiens (Human))		BDBM50471318
PNG
(CHEMBL2114266)
Show SMILES C[C@H](N)Cn1ccc2c(Cl)c(F)ccc12 |r|
Show InChI InChI=1S/C11H12ClFN2/c1-7(14)6-15-5-4-8-10(15)3-2-9(13)11(8)12/h2-5,7H,6,14H2,1H3/t7-/m0/s1
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 1.30n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Inc

Curated by ChEMBL


Assay Description
Binding affinity against human 5-hydroxytryptamine 2C receptor using displacement of [3H]DOB

J Med Chem 40: 2762-9 (1997)


Article DOI: 10.1021/jm970030l
BindingDB Entry DOI: 10.7270/Q270845Q
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Homo sapiens (Human))		BDBM50144841
PNG
((S)-1-(6-chloro-5-fluoro-1H-indol-1-yl)propan-2-am...)
Show SMILES C[C@H](N)Cn1ccc2cc(F)c(Cl)cc12
Show InChI InChI=1S/C11H12ClFN2/c1-7(14)6-15-3-2-8-4-10(13)9(12)5-11(8)15/h2-5,7H,6,14H2,1H3/t7-/m0/s1
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 1.30n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Inc

Curated by ChEMBL


Assay Description
Binding affinity against human 5-hydroxytryptamine 2C receptor using displacement of [3H]DOB

J Med Chem 40: 2762-9 (1997)


Article DOI: 10.1021/jm970030l
BindingDB Entry DOI: 10.7270/Q270845Q
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Homo sapiens (Human))		BDBM50471329
PNG
(CHEMBL2115254)
Show SMILES C[C@@H](N)Cn1ccc2c(Cl)c(F)ccc12 |r|
Show InChI InChI=1S/C11H12ClFN2/c1-7(14)6-15-5-4-8-10(15)3-2-9(13)11(8)12/h2-5,7H,6,14H2,1H3/t7-/m1/s1
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 1.30n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Inc

Curated by ChEMBL


Assay Description
Binding affinity against human 5-hydroxytryptamine 2C receptor using displacement of [3H]DOB

J Med Chem 40: 2762-9 (1997)


Article DOI: 10.1021/jm970030l
BindingDB Entry DOI: 10.7270/Q270845Q
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50087011
PNG
(8-(5-Methyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-1-...)
Show SMILES Cc1cccc2C(CCCc12)N1CCC2(CC1)N(CNC2=O)c1ccccc1
Show InChI InChI=1S/C24H29N3O/c1-18-7-5-11-21-20(18)10-6-12-22(21)26-15-13-24(14-16-26)23(28)25-17-27(24)19-8-3-2-4-9-19/h2-5,7-9,11,22H,6,10,12-17H2,1H3,(H,25,28)
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 1.40n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Competitive binding affinity against transfected HEK293 cells expressing human Opioid receptor like 1

J Med Chem 43: 1329-38 (2001)


BindingDB Entry DOI: 10.7270/Q2ZG6SZG
More data for this
Ligand-Target Pair
Nociceptin receptor


(RAT)		BDBM50087690
PNG
(8-Bicyclohexyl-4-yl-1-phenyl-1,3,8-triaza-spiro[4....)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)[C@@H]1CC[C@@H](CC1)C1CCCCC1 |wU:17.19,20.26,(14.26,-1.31,;14.73,-2.76,;16.19,-3.25,;16.19,-4.79,;14.72,-5.26,;14.26,-6.7,;12.74,-7.03,;12.27,-8.49,;13.3,-9.64,;14.8,-9.32,;15.28,-7.85,;13.82,-4.01,;13.07,-2.67,;11.53,-2.68,;10.76,-4.02,;11.53,-5.34,;13.07,-5.34,;9.22,-4.02,;8.45,-2.69,;6.91,-2.69,;6.14,-4.02,;6.91,-5.35,;8.47,-5.35,;4.6,-4.01,;3.85,-5.35,;2.29,-5.34,;1.54,-4,;2.31,-2.67,;3.85,-2.68,)|
Show InChI InChI=1S/C25H37N3O/c29-24-25(28(19-26-24)23-9-5-2-6-10-23)15-17-27(18-16-25)22-13-11-21(12-14-22)20-7-3-1-4-8-20/h2,5-6,9-10,20-22H,1,3-4,7-8,11-19H2,(H,26,29)/t21-,22+
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 1.5n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [leucyl-3H]-OFQ to membrane of human embryonic kidney 293 cells overexpressing rat Opioid receptor like 1

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Rattus norvegicus (rat))		BDBM50087690
PNG
(8-Bicyclohexyl-4-yl-1-phenyl-1,3,8-triaza-spiro[4....)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)[C@@H]1CC[C@@H](CC1)C1CCCCC1 |wU:17.19,20.26,(14.26,-1.31,;14.73,-2.76,;16.19,-3.25,;16.19,-4.79,;14.72,-5.26,;14.26,-6.7,;12.74,-7.03,;12.27,-8.49,;13.3,-9.64,;14.8,-9.32,;15.28,-7.85,;13.82,-4.01,;13.07,-2.67,;11.53,-2.68,;10.76,-4.02,;11.53,-5.34,;13.07,-5.34,;9.22,-4.02,;8.45,-2.69,;6.91,-2.69,;6.14,-4.02,;6.91,-5.35,;8.47,-5.35,;4.6,-4.01,;3.85,-5.35,;2.29,-5.34,;1.54,-4,;2.31,-2.67,;3.85,-2.68,)|
Show InChI InChI=1S/C25H37N3O/c29-24-25(28(19-26-24)23-9-5-2-6-10-23)15-17-27(18-16-25)22-13-11-21(12-14-22)20-7-3-1-4-8-20/h2,5-6,9-10,20-22H,1,3-4,7-8,11-19H2,(H,26,29)/t21-,22+
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 1.5n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [N-allyl-2-3-3H]-naloxone to membrane of baby hamster kidney cells infected with forest virus encoding the...

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474324
PNG
(CHEMBL2112346)
Show SMILES [H][C@]12CN(CC3CC3)C[C@@]1([H])C1(CCN(CC1)[C@@H]1CC[C@@H](CC1)C(C)C)N(C2)c1ccc(F)cc1 |wU:17.19,20.26,9.11,1.0,(11.12,-5.64,;10.02,-4.57,;11.26,-3.66,;10.79,-2.21,;11.72,-.96,;13.24,-1.13,;14.47,-2.03,;14.65,-.51,;9.25,-2.2,;8.77,-3.66,;7.74,-2.52,;7.53,-4.57,;6.62,-3.32,;5.09,-3.48,;4.46,-4.89,;5.36,-6.13,;6.9,-5.97,;2.93,-5.05,;2.03,-3.8,;.5,-3.97,;-.13,-5.36,;.78,-6.62,;2.31,-6.46,;-1.67,-5.53,;-2.31,-6.94,;-2.58,-4.27,;8.01,-6.04,;9.55,-6.04,;7.16,-7.32,;5.62,-7.23,;4.78,-8.51,;5.46,-9.9,;4.69,-11.23,;6.99,-9.99,;7.86,-8.7,)|
Show InChI InChI=1S/C29H44FN3/c1-21(2)23-5-9-26(10-6-23)32-15-13-29(14-16-32)28-20-31(17-22-3-4-22)18-24(28)19-33(29)27-11-7-25(30)8-12-27/h7-8,11-12,21-24,26,28H,3-6,9-10,13-20H2,1-2H3/t23-,24-,26+,28-/m1/s1
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 1.70n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474326
PNG
(CHEMBL2112347)
Show SMILES [H][C@]12CN(C[C@@]1([H])C1(CCN(CC1)[C@@H]1CC[C@@H](CC1)C(C)C)N(C2)c1ccccc1)c1ccccc1 |wU:13.14,16.21,1.0,5.6,(10.85,-8.1,;9.73,-7.03,;10.99,-6.12,;10.52,-4.66,;8.99,-4.65,;8.5,-6.12,;7.48,-4.96,;7.26,-7.01,;6.63,-8.42,;5.1,-8.58,;4.2,-7.34,;4.82,-5.93,;6.35,-5.77,;2.66,-7.5,;1.75,-6.24,;.23,-6.41,;-.4,-7.8,;.51,-9.06,;2.03,-8.89,;-1.93,-7.96,;-2.57,-9.38,;-2.83,-6.72,;7.73,-8.48,;9.27,-8.48,;6.89,-9.75,;7.58,-11.14,;6.73,-12.43,;5.2,-12.34,;4.51,-10.94,;5.36,-9.66,;11.43,-3.4,;12.98,-3.59,;13.9,-2.33,;13.27,-.92,;11.72,-.75,;10.8,-2,)|
Show InChI InChI=1S/C31H43N3/c1-24(2)25-13-15-28(16-14-25)32-19-17-31(18-20-32)30-23-33(27-9-5-3-6-10-27)21-26(30)22-34(31)29-11-7-4-8-12-29/h3-12,24-26,28,30H,13-23H2,1-2H3/t25-,26-,28+,30-/m1/s1
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 1.70n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
Nociceptin receptor


(RAT)		BDBM50087684
PNG
(8-Cyclooctyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCC1
Show InChI InChI=1S/C21H31N3O/c25-20-21(24(17-22-20)19-11-7-4-8-12-19)13-15-23(16-14-21)18-9-5-2-1-3-6-10-18/h4,7-8,11-12,18H,1-3,5-6,9-10,13-17H2,(H,22,25)
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 1.90n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [leucyl-3H]-OFQ to membrane of human embryonic kidney 293 cells overexpressing rat Opioid receptor like 1

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Nociceptin receptor


(RAT)		BDBM50087693
PNG
(1-Phenyl-8-(4-propyl-cyclohexyl)-1,3,8-triaza-spir...)
Show SMILES CCC[C@H]1CC[C@H](CC1)N1CCC2(CC1)N(CNC2=O)c1ccccc1 |wU:6.9,3.2,(1.92,-2.67,;3.46,-2.68,;4.23,-4.01,;5.77,-4.02,;6.54,-2.69,;8.08,-2.69,;8.83,-4.02,;8.08,-5.35,;6.54,-5.35,;10.37,-4.02,;11.14,-2.68,;12.68,-2.67,;13.45,-4.01,;12.68,-5.34,;11.14,-5.34,;14.33,-5.26,;15.8,-4.79,;15.8,-3.25,;14.36,-2.76,;13.87,-1.31,;13.87,-6.7,;12.35,-7.03,;11.88,-8.49,;12.91,-9.64,;14.43,-9.32,;14.89,-7.85,)|
Show InChI InChI=1S/C22H33N3O/c1-2-6-18-9-11-19(12-10-18)24-15-13-22(14-16-24)21(26)23-17-25(22)20-7-4-3-5-8-20/h3-5,7-8,18-19H,2,6,9-17H2,1H3,(H,23,26)/t18-,19+
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 2n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [leucyl-3H]-OFQ to membrane of human embryonic kidney 293 cells overexpressing rat Opioid receptor like 1

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Homo sapiens (Human))		BDBM50471312
PNG
(CHEMBL313856)
Show SMILES CC(N)Cn1ccc2cc(Cl)c(F)cc12
Show InChI InChI=1S/C11H12ClFN2/c1-7(14)6-15-3-2-8-4-9(12)10(13)5-11(8)15/h2-5,7H,6,14H2,1H3
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 2n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Inc

Curated by ChEMBL


Assay Description
Binding affinity against human 5-hydroxytryptamine 2C receptor using displacement of [3H]DOB

J Med Chem 40: 2762-9 (1997)


Article DOI: 10.1021/jm970030l
BindingDB Entry DOI: 10.7270/Q270845Q
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474323
PNG
(CHEMBL2112341)
Show SMILES [H][C@]12CN(CCN3CCOCC3)C[C@@]1([H])C1(CCN(CC1)[C@@H]1CC[C@@H](CC1)C(C)C)N(C2)c1ccccc1 |wU:21.23,24.30,1.0,13.15,(8.25,-5.32,;7.14,-4.25,;8.39,-3.34,;7.92,-1.87,;8.84,-.63,;10.37,-.79,;11.27,.44,;10.67,1.86,;11.56,3.09,;13.1,2.93,;13.73,1.53,;12.81,.28,;6.38,-1.87,;5.89,-3.34,;4.87,-2.19,;4.64,-4.24,;3.73,-2.99,;2.21,-3.15,;1.58,-4.55,;2.49,-5.81,;4.01,-5.64,;.05,-4.71,;-.85,-3.47,;-2.39,-3.63,;-3.02,-5.04,;-2.11,-6.29,;-.57,-6.13,;-4.56,-5.19,;-5.45,-3.94,;-5.19,-6.6,;5.13,-5.71,;6.67,-5.71,;4.29,-6.99,;2.75,-6.89,;1.89,-8.16,;2.59,-9.56,;4.12,-9.65,;4.97,-8.37,)|
Show InChI InChI=1S/C31H50N4O/c1-25(2)26-8-10-28(11-9-26)34-14-12-31(13-15-34)30-24-33(17-16-32-18-20-36-21-19-32)22-27(30)23-35(31)29-6-4-3-5-7-29/h3-7,25-28,30H,8-24H2,1-2H3/t26-,27-,28+,30-/m1/s1
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 2.10n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474325
PNG
(CHEMBL2112343)
Show SMILES [H][C@]12CN(Cc3ccccc3)C[C@@]1([H])C1(CCN(CC1)[C@@H]1CC[C@@H](CC1)C(C)C)N(C2)c1ccccc1 |wU:20.22,23.29,12.14,1.0,(8.65,-5.09,;7.53,-4.02,;8.79,-3.11,;8.32,-1.64,;9.23,-.4,;10.77,-.56,;11.66,.68,;13.19,.51,;13.82,-.89,;12.91,-2.13,;11.38,-1.96,;6.79,-1.64,;6.3,-3.11,;5.27,-1.96,;5.06,-4.01,;4.43,-5.41,;2.9,-5.58,;1.99,-4.32,;2.62,-2.92,;4.15,-2.76,;.45,-4.48,;-.46,-3.24,;-1.98,-3.4,;-2.61,-4.81,;-1.7,-6.06,;-.18,-5.89,;-4.15,-4.96,;-5.05,-3.71,;-4.79,-6.37,;5.53,-5.47,;7.07,-5.47,;4.69,-6.76,;3.15,-6.66,;2.31,-7.93,;2.99,-9.33,;4.53,-9.42,;5.38,-8.14,)|
Show InChI InChI=1S/C32H45N3/c1-25(2)27-13-15-29(16-14-27)34-19-17-32(18-20-34)31-24-33(21-26-9-5-3-6-10-26)22-28(31)23-35(32)30-11-7-4-8-12-30/h3-12,25,27-29,31H,13-24H2,1-2H3/t27-,28-,29+,31-/m1/s1
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 2.10n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Rattus norvegicus (rat))		BDBM50087692
PNG
(8-Cyclodecyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCCCC1
Show InChI InChI=1S/C23H35N3O/c27-22-23(26(19-24-22)21-13-9-6-10-14-21)15-17-25(18-16-23)20-11-7-4-2-1-3-5-8-12-20/h6,9-10,13-14,20H,1-5,7-8,11-12,15-19H2,(H,24,27)
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 2.10n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [N-allyl-2-3-3H]-naloxone to membrane of baby hamster kidney cells infected with forest virus encoding the...

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50087015
PNG
(1-Phenyl-8-(1,2,3,4-tetrahydro-naphthalen-1-yl)-1,...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCc2ccccc12
Show InChI InChI=1S/C23H27N3O/c27-22-23(26(17-24-22)19-9-2-1-3-10-19)13-15-25(16-14-23)21-12-6-8-18-7-4-5-11-20(18)21/h1-5,7,9-11,21H,6,8,12-17H2,(H,24,27)
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 2.10n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Competitive binding affinity against transfected HEK293 cells expressing Opioid receptor like 1

J Med Chem 43: 1329-38 (2001)


BindingDB Entry DOI: 10.7270/Q2ZG6SZG
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50474327
PNG
(CHEMBL2112344)
Show SMILES [H][C@]12CNC[C@@]1([H])C1(CCN(CC1)[C@@H]1CC[C@@H](CC1)C(C)C)N(C2)c1ccccc1 |wU:13.14,16.21,1.0,5.6,(6.85,-4.97,;5.74,-3.9,;6.99,-2.99,;6.52,-1.52,;4.98,-1.52,;4.5,-2.99,;3.47,-1.84,;3.25,-3.89,;2.62,-5.29,;1.09,-5.46,;.19,-4.2,;.82,-2.8,;2.34,-2.64,;-1.34,-4.36,;-2.25,-3.12,;-3.79,-3.28,;-4.42,-4.69,;-3.51,-5.94,;-1.97,-5.78,;-5.95,-4.84,;-6.85,-3.59,;-6.58,-6.25,;3.73,-5.36,;5.27,-5.36,;2.89,-6.64,;1.35,-6.54,;.5,-7.81,;1.19,-9.21,;2.72,-9.3,;3.57,-8.02,)|
Show InChI InChI=1S/C25H39N3/c1-19(2)20-8-10-22(11-9-20)27-14-12-25(13-15-27)24-17-26-16-21(24)18-28(25)23-6-4-3-5-7-23/h3-7,19-22,24,26H,8-18H2,1-2H3/t20-,21-,22+,24-/m1/s1
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 2.20n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition of N/OFQ binding to human Orphanin FQ receptor (Nociceptin/Orphanin)

J Med Chem 46: 255-64 (2003)


Article DOI: 10.1021/jm0209174
BindingDB Entry DOI: 10.7270/Q2GH9MQD
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50087002
PNG
(1-Phenyl-8-(1,2,3,4-tetrahydro-naphthalen-1-yl)-1,...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)[C@@H]1CCCc2ccccc12
Show InChI InChI=1S/C23H27N3O/c27-22-23(26(17-24-22)19-9-2-1-3-10-19)13-15-25(16-14-23)21-12-6-8-18-7-4-5-11-20(18)21/h1-5,7,9-11,21H,6,8,12-17H2,(H,24,27)/t21-/m1/s1
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 2.5n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Competitive binding affinity against transfected HEK293 cells expressing Opioid receptor like 1

J Med Chem 43: 1329-38 (2001)


BindingDB Entry DOI: 10.7270/Q2ZG6SZG
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50087022
PNG
(8-Indan-2-yl-1-phenyl-1,3,8-triaza-spiro[4.5]decan...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1Cc2ccccc2C1
Show InChI InChI=1S/C22H25N3O/c26-21-22(25(16-23-21)19-8-2-1-3-9-19)10-12-24(13-11-22)20-14-17-6-4-5-7-18(17)15-20/h1-9,20H,10-16H2,(H,23,26)
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 2.5n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Competitive binding affinity against transfected HEK293 cells expressing human Opioid receptor like 1

J Med Chem 43: 1329-38 (2001)


BindingDB Entry DOI: 10.7270/Q2ZG6SZG
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Homo sapiens (Human))		BDBM50087004
PNG
(8-(5,8-Dichloro-1,2,3,4-tetrahydro-naphthalen-2-yl...)
Show SMILES CN1CN(c2ccccc2)C2(CCN(CC2)C2CCc3c(Cl)ccc(Cl)c3C2)C1=O
Show InChI InChI=1S/C24H27Cl2N3O/c1-27-16-29(17-5-3-2-4-6-17)24(23(27)30)11-13-28(14-12-24)18-7-8-19-20(15-18)22(26)10-9-21(19)25/h2-6,9-10,18H,7-8,11-16H2,1H3
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 2.60n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Competitive binding displacement analyses was performed from permanently transfected HEK293 cells expressing human Opioid receptor mu 1

J Med Chem 43: 1329-38 (2001)


BindingDB Entry DOI: 10.7270/Q2ZG6SZG
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50087020
PNG
(8-(5,8-Dichloro-1,2,3,4-tetrahydro-naphthalen-2-yl...)
Show SMILES Clc1ccc(Cl)c2C[C@H](CCc12)N1CCC2(CC1)N(CNC2=O)c1ccccc1
Show InChI InChI=1S/C23H25Cl2N3O/c24-20-8-9-21(25)19-14-17(6-7-18(19)20)27-12-10-23(11-13-27)22(29)26-15-28(23)16-4-2-1-3-5-16/h1-5,8-9,17H,6-7,10-15H2,(H,26,29)/t17-/m0/s1
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 2.80n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Effective concentration required to stimulate binding of GTPgammaS to Opioid receptor like 1 was determined using scintillation proximity assay

J Med Chem 43: 1329-38 (2001)


BindingDB Entry DOI: 10.7270/Q2ZG6SZG
More data for this
Ligand-Target Pair
Nociceptin receptor


(Homo sapiens (Human))		BDBM50087012
PNG
(8-(5-Chloro-1,2,3,4-tetrahydro-naphthalen-2-yl)-1-...)
Show SMILES Clc1cccc2CC(CCc12)N1CCC2(CC1)N(CNC2=O)c1ccccc1
Show InChI InChI=1S/C23H26ClN3O/c24-21-8-4-5-17-15-19(9-10-20(17)21)26-13-11-23(12-14-26)22(28)25-16-27(23)18-6-2-1-3-7-18/h1-8,19H,9-16H2,(H,25,28)
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 2.90n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Effective concentration required to stimulate binding of GTPgammaS to Opioid receptor like 1 was determined using scintillation proximity assay

J Med Chem 43: 1329-38 (2001)


BindingDB Entry DOI: 10.7270/Q2ZG6SZG
More data for this
Ligand-Target Pair
Kappa-type opioid receptor


(Rattus norvegicus (rat))		BDBM50087685
PNG
(8-Cyclododecyl-1-phenyl-1,3,8-triaza-spiro[4.5]dec...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCCCCCC1
Show InChI InChI=1S/C25H39N3O/c29-24-25(28(21-26-24)23-15-11-8-12-16-23)17-19-27(20-18-25)22-13-9-6-4-2-1-3-5-7-10-14-22/h8,11-12,15-16,22H,1-7,9-10,13-14,17-21H2,(H,26,29)
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PubMed
 2.90n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [N-allyl-2-3-3H]-naloxone to membrane of baby hamster kidney cells infected with forest virus encoding the...

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
Mu-type opioid receptor


(Rattus norvegicus (rat))		BDBM50087687
PNG
(8-Cyclononyl-1-phenyl-1,3,8-triaza-spiro[4.5]decan...)
Show SMILES O=C1NCN(c2ccccc2)C11CCN(CC1)C1CCCCCCCC1
Show InChI InChI=1S/C22H33N3O/c26-21-22(25(18-23-21)20-12-8-5-9-13-20)14-16-24(17-15-22)19-10-6-3-1-2-4-7-11-19/h5,8-9,12-13,19H,1-4,6-7,10-11,14-18H2,(H,23,26)
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PubMed
 3.20n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Ltd.

Curated by ChEMBL


Assay Description
Inhibition against binding of radioligand [N-allyl-2-3-3H]-naloxone to membrane of baby hamster kidney cells infected with forest virus encoding the...

Bioorg Med Chem Lett 10: 831-4 (2000)


BindingDB Entry DOI: 10.7270/Q2N29XG2
More data for this
Ligand-Target Pair
5-hydroxytryptamine receptor 2C


(Homo sapiens (Human))		BDBM85863
PNG
(CAS_170493-63-7 | NSC_3045228 | Ro 600332)
Show SMILES CC(N)Cn1ccc2c1-c1cc(C)ccc1C2(C)C
Show InChI InChI=1S/C17H22N2/c1-11-5-6-14-13(9-11)16-15(17(14,3)4)7-8-19(16)10-12(2)18/h5-9,12H,10,18H2,1-4H3
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PubMed
 3.20n/an/an/an/an/an/an/an/a



F. Hoffmann-La Roche Inc

Curated by ChEMBL


Assay Description
Binding affinity against human 5-hydroxytryptamine 2C receptor using displacement of [3H]DOB

J Med Chem 40: 2762-9 (1997)


Article DOI: 10.1021/jm970030l
BindingDB Entry DOI: 10.7270/Q270845Q
More data for this
Ligand-Target Pair
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