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BDBM50454568 CHEMBL263948

SMILES: CSCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(C)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(N)=O

InChI Key: InChIKey=WHNFPRLDDSXQCL-FUIFCCQZSA-N

Data: 4 IC50  1 EC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50454568   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Melanocortin receptor 5 (MC5R)


(Homo sapiens (Human))
BDBM50454568
PNG
(CHEMBL263948)
Show SMILES CSCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(C)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(N)=O |wU:8.10,77.79,36.36,111.116,26.29,95.99,wD:107.113,14.23,45.45,55.56,4.4,66.68,(7.2,-9.08,;5.9,-8.23,;5.99,-6.69,;4.69,-5.85,;4.77,-4.32,;3.48,-3.48,;2.1,-4.19,;2.03,-5.73,;.8,-3.35,;.89,-1.82,;2.27,-1.1,;-.56,-4.06,;-1.86,-3.21,;-1.77,-1.68,;-3.23,-3.92,;-3.32,-5.46,;-2.02,-6.3,;-2.09,-7.83,;-.79,-8.66,;.58,-7.97,;1.87,-8.8,;.66,-6.43,;-.64,-5.6,;-4.52,-3.08,;-5.88,-3.78,;-5.95,-5.32,;-7.19,-2.94,;-7.1,-1.41,;-5.74,-.71,;-8.56,-3.64,;-8.66,-5.18,;-10.01,-5.88,;-7.35,-6.02,;6.13,-3.62,;6.22,-2.08,;7.44,-4.46,;8.81,-3.76,;8.88,-2.22,;10.26,-1.51,;10.33,.02,;9.04,.86,;11.7,.74,;10.09,-4.6,;10.02,-6.13,;11.47,-3.9,;12.76,-4.74,;12.69,-6.27,;13.98,-7.1,;14.05,-8.64,;15.54,-9.04,;16.38,-7.74,;15.42,-6.54,;14.14,-4.03,;14.22,-2.49,;15.43,-4.85,;16.8,-4.15,;16.87,-2.62,;18.24,-1.92,;19.55,-2.76,;20.92,-2.06,;20.99,-.51,;19.7,.32,;18.33,-.38,;18.1,-4.99,;18.03,-6.53,;19.47,-4.29,;20.76,-5.13,;20.68,-6.67,;21.97,-7.51,;21.9,-9.04,;23.2,-9.88,;23.11,-11.42,;24.41,-12.26,;21.74,-12.12,;22.13,-4.43,;22.22,-2.9,;23.41,-5.27,;24.79,-4.57,;24.87,-3.04,;24.09,-1.68,;22.58,-1.41,;22.37,.12,;23.76,.78,;24.21,2.26,;25.71,2.61,;26.77,1.49,;26.33,.02,;24.84,-.33,;26.09,-5.4,;26.02,-6.94,;27.47,-4.7,;28.76,-5.53,;30.12,-4.83,;30.21,-3.29,;31.43,-5.67,;32.8,-4.97,;32.87,-3.43,;34.25,-2.73,;34.31,-1.2,;35.69,-.49,;35.77,1.05,;34.08,-5.81,;34.01,-7.34,;35.59,-5.22,;35.76,-6.74,;37.27,-7.04,;38.02,-5.71,;36.99,-4.57,;37.27,-3.06,;36.12,-2.03,;38.74,-2.57,;39.04,-1.06,;37.88,-.03,;38.18,1.47,;36.41,-.54,;40.5,-.56,;40.79,.95,;41.65,-1.57,)|
Show InChI InChI=1S/C77H109N21O19S/c1-42(2)64(65(79)106)97-75(116)61-20-13-30-98(61)76(117)54(18-10-11-28-78)88-62(103)38-85-66(107)57(34-46-36-84-50-17-9-8-16-49(46)50)94-67(108)51(19-12-29-83-77(80)81)89-70(111)55(32-44-14-6-5-7-15-44)92-72(113)58(35-47-37-82-41-86-47)95-68(109)52(25-26-63(104)105)90-69(110)53(27-31-118-4)91-74(115)60(40-100)96-71(112)56(33-45-21-23-48(102)24-22-45)93-73(114)59(39-99)87-43(3)101/h5-9,14-17,21-24,36-37,41-42,51-61,64,84,99-100,102H,10-13,18-20,25-35,38-40,78H2,1-4H3,(H2,79,106)(H,82,86)(H,85,107)(H,87,101)(H,88,103)(H,89,111)(H,90,110)(H,91,115)(H,92,113)(H,93,114)(H,94,108)(H,95,109)(H,96,112)(H,97,116)(H,104,105)(H4,80,81,83)/t51-,52-,53-,54-,55+,56-,57-,58-,59-,60-,61-,64-/m0/s1
UniProtKB/SwissProt

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CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 557n/an/an/an/an/an/a



University of Michigan Medical Center

Curated by ChEMBL


Assay Description
Displacement of [125I]NDP-MSH from Melanocortin 5 receptor at 10 uM


J Med Chem 40: 2133-9 (1997)


Article DOI: 10.1021/jm960840h
BindingDB Entry DOI: 10.7270/Q28K79R6
More data for this
Ligand-Target Pair
Melanocortin receptor 4


(Homo sapiens (Human))
BDBM50454568
PNG
(CHEMBL263948)
Show SMILES CSCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(C)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(N)=O |wU:8.10,77.79,36.36,111.116,26.29,95.99,wD:107.113,14.23,45.45,55.56,4.4,66.68,(7.2,-9.08,;5.9,-8.23,;5.99,-6.69,;4.69,-5.85,;4.77,-4.32,;3.48,-3.48,;2.1,-4.19,;2.03,-5.73,;.8,-3.35,;.89,-1.82,;2.27,-1.1,;-.56,-4.06,;-1.86,-3.21,;-1.77,-1.68,;-3.23,-3.92,;-3.32,-5.46,;-2.02,-6.3,;-2.09,-7.83,;-.79,-8.66,;.58,-7.97,;1.87,-8.8,;.66,-6.43,;-.64,-5.6,;-4.52,-3.08,;-5.88,-3.78,;-5.95,-5.32,;-7.19,-2.94,;-7.1,-1.41,;-5.74,-.71,;-8.56,-3.64,;-8.66,-5.18,;-10.01,-5.88,;-7.35,-6.02,;6.13,-3.62,;6.22,-2.08,;7.44,-4.46,;8.81,-3.76,;8.88,-2.22,;10.26,-1.51,;10.33,.02,;9.04,.86,;11.7,.74,;10.09,-4.6,;10.02,-6.13,;11.47,-3.9,;12.76,-4.74,;12.69,-6.27,;13.98,-7.1,;14.05,-8.64,;15.54,-9.04,;16.38,-7.74,;15.42,-6.54,;14.14,-4.03,;14.22,-2.49,;15.43,-4.85,;16.8,-4.15,;16.87,-2.62,;18.24,-1.92,;19.55,-2.76,;20.92,-2.06,;20.99,-.51,;19.7,.32,;18.33,-.38,;18.1,-4.99,;18.03,-6.53,;19.47,-4.29,;20.76,-5.13,;20.68,-6.67,;21.97,-7.51,;21.9,-9.04,;23.2,-9.88,;23.11,-11.42,;24.41,-12.26,;21.74,-12.12,;22.13,-4.43,;22.22,-2.9,;23.41,-5.27,;24.79,-4.57,;24.87,-3.04,;24.09,-1.68,;22.58,-1.41,;22.37,.12,;23.76,.78,;24.21,2.26,;25.71,2.61,;26.77,1.49,;26.33,.02,;24.84,-.33,;26.09,-5.4,;26.02,-6.94,;27.47,-4.7,;28.76,-5.53,;30.12,-4.83,;30.21,-3.29,;31.43,-5.67,;32.8,-4.97,;32.87,-3.43,;34.25,-2.73,;34.31,-1.2,;35.69,-.49,;35.77,1.05,;34.08,-5.81,;34.01,-7.34,;35.59,-5.22,;35.76,-6.74,;37.27,-7.04,;38.02,-5.71,;36.99,-4.57,;37.27,-3.06,;36.12,-2.03,;38.74,-2.57,;39.04,-1.06,;37.88,-.03,;38.18,1.47,;36.41,-.54,;40.5,-.56,;40.79,.95,;41.65,-1.57,)|
Show InChI InChI=1S/C77H109N21O19S/c1-42(2)64(65(79)106)97-75(116)61-20-13-30-98(61)76(117)54(18-10-11-28-78)88-62(103)38-85-66(107)57(34-46-36-84-50-17-9-8-16-49(46)50)94-67(108)51(19-12-29-83-77(80)81)89-70(111)55(32-44-14-6-5-7-15-44)92-72(113)58(35-47-37-82-41-86-47)95-68(109)52(25-26-63(104)105)90-69(110)53(27-31-118-4)91-74(115)60(40-100)96-71(112)56(33-45-21-23-48(102)24-22-45)93-73(114)59(39-99)87-43(3)101/h5-9,14-17,21-24,36-37,41-42,51-61,64,84,99-100,102H,10-13,18-20,25-35,38-40,78H2,1-4H3,(H2,79,106)(H,82,86)(H,85,107)(H,87,101)(H,88,103)(H,89,111)(H,90,110)(H,91,115)(H,92,113)(H,93,114)(H,94,108)(H,95,109)(H,96,112)(H,97,116)(H,104,105)(H4,80,81,83)/t51-,52-,53-,54-,55+,56-,57-,58-,59-,60-,61-,64-/m0/s1
PDB

KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 39n/an/an/an/an/an/a



University of Michigan Medical Center

Curated by ChEMBL


Assay Description
Displacement of [125I]NDP-MSH from Melanocortin 4 receptor at 10 uM


J Med Chem 40: 2133-9 (1997)


Article DOI: 10.1021/jm960840h
BindingDB Entry DOI: 10.7270/Q28K79R6
More data for this
Ligand-Target Pair
Melanocyte-stimulating hormone receptor


(Homo sapiens (Human))
BDBM50454568
PNG
(CHEMBL263948)
Show SMILES CSCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(C)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(N)=O |wU:8.10,77.79,36.36,111.116,26.29,95.99,wD:107.113,14.23,45.45,55.56,4.4,66.68,(7.2,-9.08,;5.9,-8.23,;5.99,-6.69,;4.69,-5.85,;4.77,-4.32,;3.48,-3.48,;2.1,-4.19,;2.03,-5.73,;.8,-3.35,;.89,-1.82,;2.27,-1.1,;-.56,-4.06,;-1.86,-3.21,;-1.77,-1.68,;-3.23,-3.92,;-3.32,-5.46,;-2.02,-6.3,;-2.09,-7.83,;-.79,-8.66,;.58,-7.97,;1.87,-8.8,;.66,-6.43,;-.64,-5.6,;-4.52,-3.08,;-5.88,-3.78,;-5.95,-5.32,;-7.19,-2.94,;-7.1,-1.41,;-5.74,-.71,;-8.56,-3.64,;-8.66,-5.18,;-10.01,-5.88,;-7.35,-6.02,;6.13,-3.62,;6.22,-2.08,;7.44,-4.46,;8.81,-3.76,;8.88,-2.22,;10.26,-1.51,;10.33,.02,;9.04,.86,;11.7,.74,;10.09,-4.6,;10.02,-6.13,;11.47,-3.9,;12.76,-4.74,;12.69,-6.27,;13.98,-7.1,;14.05,-8.64,;15.54,-9.04,;16.38,-7.74,;15.42,-6.54,;14.14,-4.03,;14.22,-2.49,;15.43,-4.85,;16.8,-4.15,;16.87,-2.62,;18.24,-1.92,;19.55,-2.76,;20.92,-2.06,;20.99,-.51,;19.7,.32,;18.33,-.38,;18.1,-4.99,;18.03,-6.53,;19.47,-4.29,;20.76,-5.13,;20.68,-6.67,;21.97,-7.51,;21.9,-9.04,;23.2,-9.88,;23.11,-11.42,;24.41,-12.26,;21.74,-12.12,;22.13,-4.43,;22.22,-2.9,;23.41,-5.27,;24.79,-4.57,;24.87,-3.04,;24.09,-1.68,;22.58,-1.41,;22.37,.12,;23.76,.78,;24.21,2.26,;25.71,2.61,;26.77,1.49,;26.33,.02,;24.84,-.33,;26.09,-5.4,;26.02,-6.94,;27.47,-4.7,;28.76,-5.53,;30.12,-4.83,;30.21,-3.29,;31.43,-5.67,;32.8,-4.97,;32.87,-3.43,;34.25,-2.73,;34.31,-1.2,;35.69,-.49,;35.77,1.05,;34.08,-5.81,;34.01,-7.34,;35.59,-5.22,;35.76,-6.74,;37.27,-7.04,;38.02,-5.71,;36.99,-4.57,;37.27,-3.06,;36.12,-2.03,;38.74,-2.57,;39.04,-1.06,;37.88,-.03,;38.18,1.47,;36.41,-.54,;40.5,-.56,;40.79,.95,;41.65,-1.57,)|
Show InChI InChI=1S/C77H109N21O19S/c1-42(2)64(65(79)106)97-75(116)61-20-13-30-98(61)76(117)54(18-10-11-28-78)88-62(103)38-85-66(107)57(34-46-36-84-50-17-9-8-16-49(46)50)94-67(108)51(19-12-29-83-77(80)81)89-70(111)55(32-44-14-6-5-7-15-44)92-72(113)58(35-47-37-82-41-86-47)95-68(109)52(25-26-63(104)105)90-69(110)53(27-31-118-4)91-74(115)60(40-100)96-71(112)56(33-45-21-23-48(102)24-22-45)93-73(114)59(39-99)87-43(3)101/h5-9,14-17,21-24,36-37,41-42,51-61,64,84,99-100,102H,10-13,18-20,25-35,38-40,78H2,1-4H3,(H2,79,106)(H,82,86)(H,85,107)(H,87,101)(H,88,103)(H,89,111)(H,90,110)(H,91,115)(H,92,113)(H,93,114)(H,94,108)(H,95,109)(H,96,112)(H,97,116)(H,104,105)(H4,80,81,83)/t51-,52-,53-,54-,55+,56-,57-,58-,59-,60-,61-,64-/m0/s1
PDB

KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
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CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 0.190n/an/an/an/a



University of Michigan Medical Center

Curated by ChEMBL


Assay Description
effective concentration of peptide at 50% maximal cAMP accumulation on Melanocortin 1 receptor


J Med Chem 40: 2133-9 (1997)


Article DOI: 10.1021/jm960840h
BindingDB Entry DOI: 10.7270/Q28K79R6
More data for this
Ligand-Target Pair
Melanocyte-stimulating hormone receptor


(Homo sapiens (Human))
BDBM50454568
PNG
(CHEMBL263948)
Show SMILES CSCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(C)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(N)=O |wU:8.10,77.79,36.36,111.116,26.29,95.99,wD:107.113,14.23,45.45,55.56,4.4,66.68,(7.2,-9.08,;5.9,-8.23,;5.99,-6.69,;4.69,-5.85,;4.77,-4.32,;3.48,-3.48,;2.1,-4.19,;2.03,-5.73,;.8,-3.35,;.89,-1.82,;2.27,-1.1,;-.56,-4.06,;-1.86,-3.21,;-1.77,-1.68,;-3.23,-3.92,;-3.32,-5.46,;-2.02,-6.3,;-2.09,-7.83,;-.79,-8.66,;.58,-7.97,;1.87,-8.8,;.66,-6.43,;-.64,-5.6,;-4.52,-3.08,;-5.88,-3.78,;-5.95,-5.32,;-7.19,-2.94,;-7.1,-1.41,;-5.74,-.71,;-8.56,-3.64,;-8.66,-5.18,;-10.01,-5.88,;-7.35,-6.02,;6.13,-3.62,;6.22,-2.08,;7.44,-4.46,;8.81,-3.76,;8.88,-2.22,;10.26,-1.51,;10.33,.02,;9.04,.86,;11.7,.74,;10.09,-4.6,;10.02,-6.13,;11.47,-3.9,;12.76,-4.74,;12.69,-6.27,;13.98,-7.1,;14.05,-8.64,;15.54,-9.04,;16.38,-7.74,;15.42,-6.54,;14.14,-4.03,;14.22,-2.49,;15.43,-4.85,;16.8,-4.15,;16.87,-2.62,;18.24,-1.92,;19.55,-2.76,;20.92,-2.06,;20.99,-.51,;19.7,.32,;18.33,-.38,;18.1,-4.99,;18.03,-6.53,;19.47,-4.29,;20.76,-5.13,;20.68,-6.67,;21.97,-7.51,;21.9,-9.04,;23.2,-9.88,;23.11,-11.42,;24.41,-12.26,;21.74,-12.12,;22.13,-4.43,;22.22,-2.9,;23.41,-5.27,;24.79,-4.57,;24.87,-3.04,;24.09,-1.68,;22.58,-1.41,;22.37,.12,;23.76,.78,;24.21,2.26,;25.71,2.61,;26.77,1.49,;26.33,.02,;24.84,-.33,;26.09,-5.4,;26.02,-6.94,;27.47,-4.7,;28.76,-5.53,;30.12,-4.83,;30.21,-3.29,;31.43,-5.67,;32.8,-4.97,;32.87,-3.43,;34.25,-2.73,;34.31,-1.2,;35.69,-.49,;35.77,1.05,;34.08,-5.81,;34.01,-7.34,;35.59,-5.22,;35.76,-6.74,;37.27,-7.04,;38.02,-5.71,;36.99,-4.57,;37.27,-3.06,;36.12,-2.03,;38.74,-2.57,;39.04,-1.06,;37.88,-.03,;38.18,1.47,;36.41,-.54,;40.5,-.56,;40.79,.95,;41.65,-1.57,)|
Show InChI InChI=1S/C77H109N21O19S/c1-42(2)64(65(79)106)97-75(116)61-20-13-30-98(61)76(117)54(18-10-11-28-78)88-62(103)38-85-66(107)57(34-46-36-84-50-17-9-8-16-49(46)50)94-67(108)51(19-12-29-83-77(80)81)89-70(111)55(32-44-14-6-5-7-15-44)92-72(113)58(35-47-37-82-41-86-47)95-68(109)52(25-26-63(104)105)90-69(110)53(27-31-118-4)91-74(115)60(40-100)96-71(112)56(33-45-21-23-48(102)24-22-45)93-73(114)59(39-99)87-43(3)101/h5-9,14-17,21-24,36-37,41-42,51-61,64,84,99-100,102H,10-13,18-20,25-35,38-40,78H2,1-4H3,(H2,79,106)(H,82,86)(H,85,107)(H,87,101)(H,88,103)(H,89,111)(H,90,110)(H,91,115)(H,92,113)(H,93,114)(H,94,108)(H,95,109)(H,96,112)(H,97,116)(H,104,105)(H4,80,81,83)/t51-,52-,53-,54-,55+,56-,57-,58-,59-,60-,61-,64-/m0/s1
PDB

KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

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Article
PubMed
n/an/a 6n/an/an/an/an/an/a



University of Michigan Medical Center

Curated by ChEMBL


Assay Description
Displacement of [125I]NDP-MSH from Melanocortin 1 receptor at 10 uM


J Med Chem 40: 2133-9 (1997)


Article DOI: 10.1021/jm960840h
BindingDB Entry DOI: 10.7270/Q28K79R6
More data for this
Ligand-Target Pair
Melanocortin receptor 3


(Homo sapiens (Human))
BDBM50454568
PNG
(CHEMBL263948)
Show SMILES CSCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(C)=O)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@@H](C(C)C)C(N)=O |wU:8.10,77.79,36.36,111.116,26.29,95.99,wD:107.113,14.23,45.45,55.56,4.4,66.68,(7.2,-9.08,;5.9,-8.23,;5.99,-6.69,;4.69,-5.85,;4.77,-4.32,;3.48,-3.48,;2.1,-4.19,;2.03,-5.73,;.8,-3.35,;.89,-1.82,;2.27,-1.1,;-.56,-4.06,;-1.86,-3.21,;-1.77,-1.68,;-3.23,-3.92,;-3.32,-5.46,;-2.02,-6.3,;-2.09,-7.83,;-.79,-8.66,;.58,-7.97,;1.87,-8.8,;.66,-6.43,;-.64,-5.6,;-4.52,-3.08,;-5.88,-3.78,;-5.95,-5.32,;-7.19,-2.94,;-7.1,-1.41,;-5.74,-.71,;-8.56,-3.64,;-8.66,-5.18,;-10.01,-5.88,;-7.35,-6.02,;6.13,-3.62,;6.22,-2.08,;7.44,-4.46,;8.81,-3.76,;8.88,-2.22,;10.26,-1.51,;10.33,.02,;9.04,.86,;11.7,.74,;10.09,-4.6,;10.02,-6.13,;11.47,-3.9,;12.76,-4.74,;12.69,-6.27,;13.98,-7.1,;14.05,-8.64,;15.54,-9.04,;16.38,-7.74,;15.42,-6.54,;14.14,-4.03,;14.22,-2.49,;15.43,-4.85,;16.8,-4.15,;16.87,-2.62,;18.24,-1.92,;19.55,-2.76,;20.92,-2.06,;20.99,-.51,;19.7,.32,;18.33,-.38,;18.1,-4.99,;18.03,-6.53,;19.47,-4.29,;20.76,-5.13,;20.68,-6.67,;21.97,-7.51,;21.9,-9.04,;23.2,-9.88,;23.11,-11.42,;24.41,-12.26,;21.74,-12.12,;22.13,-4.43,;22.22,-2.9,;23.41,-5.27,;24.79,-4.57,;24.87,-3.04,;24.09,-1.68,;22.58,-1.41,;22.37,.12,;23.76,.78,;24.21,2.26,;25.71,2.61,;26.77,1.49,;26.33,.02,;24.84,-.33,;26.09,-5.4,;26.02,-6.94,;27.47,-4.7,;28.76,-5.53,;30.12,-4.83,;30.21,-3.29,;31.43,-5.67,;32.8,-4.97,;32.87,-3.43,;34.25,-2.73,;34.31,-1.2,;35.69,-.49,;35.77,1.05,;34.08,-5.81,;34.01,-7.34,;35.59,-5.22,;35.76,-6.74,;37.27,-7.04,;38.02,-5.71,;36.99,-4.57,;37.27,-3.06,;36.12,-2.03,;38.74,-2.57,;39.04,-1.06,;37.88,-.03,;38.18,1.47,;36.41,-.54,;40.5,-.56,;40.79,.95,;41.65,-1.57,)|
Show InChI InChI=1S/C77H109N21O19S/c1-42(2)64(65(79)106)97-75(116)61-20-13-30-98(61)76(117)54(18-10-11-28-78)88-62(103)38-85-66(107)57(34-46-36-84-50-17-9-8-16-49(46)50)94-67(108)51(19-12-29-83-77(80)81)89-70(111)55(32-44-14-6-5-7-15-44)92-72(113)58(35-47-37-82-41-86-47)95-68(109)52(25-26-63(104)105)90-69(110)53(27-31-118-4)91-74(115)60(40-100)96-71(112)56(33-45-21-23-48(102)24-22-45)93-73(114)59(39-99)87-43(3)101/h5-9,14-17,21-24,36-37,41-42,51-61,64,84,99-100,102H,10-13,18-20,25-35,38-40,78H2,1-4H3,(H2,79,106)(H,82,86)(H,85,107)(H,87,101)(H,88,103)(H,89,111)(H,90,110)(H,91,115)(H,92,113)(H,93,114)(H,94,108)(H,95,109)(H,96,112)(H,97,116)(H,104,105)(H4,80,81,83)/t51-,52-,53-,54-,55+,56-,57-,58-,59-,60-,61-,64-/m0/s1
UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 50n/an/an/an/an/an/a



University of Michigan Medical Center

Curated by ChEMBL


Assay Description
Displacement of [125I]NDP-MSH from Melanocortin 3 receptor at 10 uM


J Med Chem 40: 2133-9 (1997)


Article DOI: 10.1021/jm960840h
BindingDB Entry DOI: 10.7270/Q28K79R6
More data for this
Ligand-Target Pair