Found 4 hits Enz. Inhib. hit(s) with Target = 'Nociceptin receptor' and Ligand = 'BDBM50274468' Target/Host
(Institution) | Ligand | Target/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 | pH | Temp
°C |
|---|
Nociceptin receptor
(RAT) | BDBM50274468
(CHEMBL510117 | FGGFTGARKSARKLWNQ)Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccccc1)[C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O |r,wU:91.92,68.68,100.103,59.59,39.44,28.28,8.13,106.107,128.131,wD:72.80,48.55,33.35,17.24,4.4,120.123,(47.19,-24.72,;47.19,-23.18,;48.53,-22.41,;45.85,-22.41,;45.85,-20.87,;44.53,-20.1,;43.18,-20.88,;43.18,-22.41,;41.85,-20.11,;41.85,-18.57,;43.18,-17.79,;43.18,-16.25,;44.52,-15.48,;44.52,-13.94,;40.52,-20.88,;39.19,-20.11,;39.19,-18.56,;37.85,-20.88,;37.85,-22.42,;39.19,-23.19,;39.19,-24.73,;40.53,-25.5,;40.53,-27.04,;39.19,-27.8,;41.86,-27.81,;36.52,-20.12,;35.18,-20.89,;35.18,-22.42,;33.85,-20.11,;33.85,-18.57,;32.52,-20.89,;31.18,-20.12,;31.18,-18.58,;29.85,-20.89,;29.85,-22.43,;31.18,-23.2,;28.52,-20.12,;27.18,-20.89,;27.18,-22.43,;25.85,-20.12,;25.85,-18.58,;27.18,-17.82,;27.18,-16.27,;28.51,-15.5,;28.51,-13.96,;24.51,-20.9,;23.18,-20.13,;23.18,-18.59,;21.84,-20.9,;21.84,-22.43,;23.18,-23.21,;23.18,-24.74,;24.52,-25.52,;24.52,-27.06,;23.18,-27.82,;25.85,-27.83,;20.51,-20.13,;19.17,-20.9,;19.17,-22.44,;17.84,-20.14,;17.84,-18.59,;16.51,-20.91,;15.17,-20.14,;15.17,-18.59,;13.84,-20.91,;12.51,-20.14,;11.17,-20.92,;11.17,-22.45,;9.84,-20.14,;8.5,-20.91,;7.17,-20.15,;7.17,-18.61,;5.84,-20.92,;5.84,-22.46,;7.17,-23.23,;8.5,-22.45,;9.84,-23.22,;9.84,-24.76,;8.51,-25.54,;7.18,-24.76,;4.5,-20.15,;3.17,-20.92,;3.17,-22.46,;1.84,-20.16,;.5,-20.93,;-.84,-20.16,;-.84,-18.62,;-2.16,-20.93,;-3.5,-20.16,;-4.84,-20.93,;-4.84,-22.47,;-6.17,-20.16,;-7.51,-20.93,;-6.17,-18.62,;-4.84,-17.85,;-3.51,-18.62,;-2.17,-17.84,;-2.17,-16.31,;-3.51,-15.54,;-4.84,-16.31,;9.84,-18.6,;8.5,-17.83,;11.17,-17.83,;47.19,-20.1,;47.19,-18.56,;48.52,-20.87,;49.86,-20.1,;49.86,-18.55,;51.19,-17.79,;52.6,-18.41,;53.62,-17.26,;52.86,-15.93,;53.33,-14.46,;52.29,-13.32,;50.79,-13.64,;50.32,-15.11,;51.35,-16.25,;51.19,-20.86,;51.19,-22.4,;52.53,-20.09,;53.86,-20.86,;53.86,-22.4,;55.2,-23.17,;56.54,-22.4,;55.2,-24.71,;55.2,-20.09,;55.2,-18.55,;56.53,-20.86,;57.86,-20.08,;57.86,-18.54,;59.2,-17.78,;59.2,-16.23,;57.85,-15.46,;60.53,-15.47,;59.2,-20.86,;60.53,-20.09,;59.2,-22.39,)| Show InChI InChI=1S/C87H134N28O22/c1-46(2)36-61(79(130)112-63(39-52-41-99-55-25-13-12-24-53(52)55)80(131)113-64(40-67(92)119)81(132)110-60(85(136)137)30-31-66(91)118)111-77(128)56(26-14-16-32-88)108-76(127)59(29-19-35-98-87(95)96)107-73(124)48(4)104-83(134)65(45-116)114-78(129)57(27-15-17-33-89)109-75(126)58(28-18-34-97-86(93)94)106-72(123)47(3)103-69(121)44-102-84(135)71(49(5)117)115-82(133)62(38-51-22-10-7-11-23-51)105-70(122)43-100-68(120)42-101-74(125)54(90)37-50-20-8-6-9-21-50/h6-13,20-25,41,46-49,54,56-65,71,99,116-117H,14-19,26-40,42-45,88-90H2,1-5H3,(H2,91,118)(H2,92,119)(H,100,120)(H,101,125)(H,102,135)(H,103,121)(H,104,134)(H,105,122)(H,106,123)(H,107,124)(H,108,127)(H,109,126)(H,110,132)(H,111,128)(H,112,130)(H,113,131)(H,114,129)(H,115,133)(H,136,137)(H4,93,94,97)(H4,95,96,98)/t47-,48-,49+,54-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,71-/m0/s1 | PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet 
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.10 | n/a | n/a | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Displacement of [3H]nociceptin from rat ORL1 receptor expressed in african green monkey COS7 cells |
Bioorg Med Chem 16: 9261-7 (2008)
Article DOI: 10.1016/j.bmc.2008.09.014
BindingDB Entry DOI: 10.7270/Q2MC90XH |
More data for this
Ligand-Target Pair | |
Nociceptin receptor
(RAT) | BDBM50274468
(CHEMBL510117 | FGGFTGARKSARKLWNQ)Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccccc1)[C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O |r,wU:91.92,68.68,100.103,59.59,39.44,28.28,8.13,106.107,128.131,wD:72.80,48.55,33.35,17.24,4.4,120.123,(47.19,-24.72,;47.19,-23.18,;48.53,-22.41,;45.85,-22.41,;45.85,-20.87,;44.53,-20.1,;43.18,-20.88,;43.18,-22.41,;41.85,-20.11,;41.85,-18.57,;43.18,-17.79,;43.18,-16.25,;44.52,-15.48,;44.52,-13.94,;40.52,-20.88,;39.19,-20.11,;39.19,-18.56,;37.85,-20.88,;37.85,-22.42,;39.19,-23.19,;39.19,-24.73,;40.53,-25.5,;40.53,-27.04,;39.19,-27.8,;41.86,-27.81,;36.52,-20.12,;35.18,-20.89,;35.18,-22.42,;33.85,-20.11,;33.85,-18.57,;32.52,-20.89,;31.18,-20.12,;31.18,-18.58,;29.85,-20.89,;29.85,-22.43,;31.18,-23.2,;28.52,-20.12,;27.18,-20.89,;27.18,-22.43,;25.85,-20.12,;25.85,-18.58,;27.18,-17.82,;27.18,-16.27,;28.51,-15.5,;28.51,-13.96,;24.51,-20.9,;23.18,-20.13,;23.18,-18.59,;21.84,-20.9,;21.84,-22.43,;23.18,-23.21,;23.18,-24.74,;24.52,-25.52,;24.52,-27.06,;23.18,-27.82,;25.85,-27.83,;20.51,-20.13,;19.17,-20.9,;19.17,-22.44,;17.84,-20.14,;17.84,-18.59,;16.51,-20.91,;15.17,-20.14,;15.17,-18.59,;13.84,-20.91,;12.51,-20.14,;11.17,-20.92,;11.17,-22.45,;9.84,-20.14,;8.5,-20.91,;7.17,-20.15,;7.17,-18.61,;5.84,-20.92,;5.84,-22.46,;7.17,-23.23,;8.5,-22.45,;9.84,-23.22,;9.84,-24.76,;8.51,-25.54,;7.18,-24.76,;4.5,-20.15,;3.17,-20.92,;3.17,-22.46,;1.84,-20.16,;.5,-20.93,;-.84,-20.16,;-.84,-18.62,;-2.16,-20.93,;-3.5,-20.16,;-4.84,-20.93,;-4.84,-22.47,;-6.17,-20.16,;-7.51,-20.93,;-6.17,-18.62,;-4.84,-17.85,;-3.51,-18.62,;-2.17,-17.84,;-2.17,-16.31,;-3.51,-15.54,;-4.84,-16.31,;9.84,-18.6,;8.5,-17.83,;11.17,-17.83,;47.19,-20.1,;47.19,-18.56,;48.52,-20.87,;49.86,-20.1,;49.86,-18.55,;51.19,-17.79,;52.6,-18.41,;53.62,-17.26,;52.86,-15.93,;53.33,-14.46,;52.29,-13.32,;50.79,-13.64,;50.32,-15.11,;51.35,-16.25,;51.19,-20.86,;51.19,-22.4,;52.53,-20.09,;53.86,-20.86,;53.86,-22.4,;55.2,-23.17,;56.54,-22.4,;55.2,-24.71,;55.2,-20.09,;55.2,-18.55,;56.53,-20.86,;57.86,-20.08,;57.86,-18.54,;59.2,-17.78,;59.2,-16.23,;57.85,-15.46,;60.53,-15.47,;59.2,-20.86,;60.53,-20.09,;59.2,-22.39,)| Show InChI InChI=1S/C87H134N28O22/c1-46(2)36-61(79(130)112-63(39-52-41-99-55-25-13-12-24-53(52)55)80(131)113-64(40-67(92)119)81(132)110-60(85(136)137)30-31-66(91)118)111-77(128)56(26-14-16-32-88)108-76(127)59(29-19-35-98-87(95)96)107-73(124)48(4)104-83(134)65(45-116)114-78(129)57(27-15-17-33-89)109-75(126)58(28-18-34-97-86(93)94)106-72(123)47(3)103-69(121)44-102-84(135)71(49(5)117)115-82(133)62(38-51-22-10-7-11-23-51)105-70(122)43-100-68(120)42-101-74(125)54(90)37-50-20-8-6-9-21-50/h6-13,20-25,41,46-49,54,56-65,71,99,116-117H,14-19,26-40,42-45,88-90H2,1-5H3,(H2,91,118)(H2,92,119)(H,100,120)(H,101,125)(H,102,135)(H,103,121)(H,104,134)(H,105,122)(H,106,123)(H,107,124)(H,108,127)(H,109,126)(H,110,132)(H,111,128)(H,112,130)(H,113,131)(H,114,129)(H,115,133)(H,136,137)(H4,93,94,97)(H4,95,96,98)/t47-,48-,49+,54-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,71-/m0/s1 | PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | 2.10 | n/a | n/a | n/a | n/a | n/a | n/a |
Kyushu University
Curated by ChEMBL
| Assay Description
Displacement of [3H]nociceptin from rat ORL1 receptor expressed in african green monkey COS7 cells by competitive binding assay |
Bioorg Med Chem 17: 5683-7 (2009)
Article DOI: 10.1016/j.bmc.2009.06.015
BindingDB Entry DOI: 10.7270/Q2GB2435 |
More data for this
Ligand-Target Pair | |
Nociceptin receptor
(RAT) | BDBM50274468
(CHEMBL510117 | FGGFTGARKSARKLWNQ)Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccccc1)[C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O |r,wU:91.92,68.68,100.103,59.59,39.44,28.28,8.13,106.107,128.131,wD:72.80,48.55,33.35,17.24,4.4,120.123,(47.19,-24.72,;47.19,-23.18,;48.53,-22.41,;45.85,-22.41,;45.85,-20.87,;44.53,-20.1,;43.18,-20.88,;43.18,-22.41,;41.85,-20.11,;41.85,-18.57,;43.18,-17.79,;43.18,-16.25,;44.52,-15.48,;44.52,-13.94,;40.52,-20.88,;39.19,-20.11,;39.19,-18.56,;37.85,-20.88,;37.85,-22.42,;39.19,-23.19,;39.19,-24.73,;40.53,-25.5,;40.53,-27.04,;39.19,-27.8,;41.86,-27.81,;36.52,-20.12,;35.18,-20.89,;35.18,-22.42,;33.85,-20.11,;33.85,-18.57,;32.52,-20.89,;31.18,-20.12,;31.18,-18.58,;29.85,-20.89,;29.85,-22.43,;31.18,-23.2,;28.52,-20.12,;27.18,-20.89,;27.18,-22.43,;25.85,-20.12,;25.85,-18.58,;27.18,-17.82,;27.18,-16.27,;28.51,-15.5,;28.51,-13.96,;24.51,-20.9,;23.18,-20.13,;23.18,-18.59,;21.84,-20.9,;21.84,-22.43,;23.18,-23.21,;23.18,-24.74,;24.52,-25.52,;24.52,-27.06,;23.18,-27.82,;25.85,-27.83,;20.51,-20.13,;19.17,-20.9,;19.17,-22.44,;17.84,-20.14,;17.84,-18.59,;16.51,-20.91,;15.17,-20.14,;15.17,-18.59,;13.84,-20.91,;12.51,-20.14,;11.17,-20.92,;11.17,-22.45,;9.84,-20.14,;8.5,-20.91,;7.17,-20.15,;7.17,-18.61,;5.84,-20.92,;5.84,-22.46,;7.17,-23.23,;8.5,-22.45,;9.84,-23.22,;9.84,-24.76,;8.51,-25.54,;7.18,-24.76,;4.5,-20.15,;3.17,-20.92,;3.17,-22.46,;1.84,-20.16,;.5,-20.93,;-.84,-20.16,;-.84,-18.62,;-2.16,-20.93,;-3.5,-20.16,;-4.84,-20.93,;-4.84,-22.47,;-6.17,-20.16,;-7.51,-20.93,;-6.17,-18.62,;-4.84,-17.85,;-3.51,-18.62,;-2.17,-17.84,;-2.17,-16.31,;-3.51,-15.54,;-4.84,-16.31,;9.84,-18.6,;8.5,-17.83,;11.17,-17.83,;47.19,-20.1,;47.19,-18.56,;48.52,-20.87,;49.86,-20.1,;49.86,-18.55,;51.19,-17.79,;52.6,-18.41,;53.62,-17.26,;52.86,-15.93,;53.33,-14.46,;52.29,-13.32,;50.79,-13.64,;50.32,-15.11,;51.35,-16.25,;51.19,-20.86,;51.19,-22.4,;52.53,-20.09,;53.86,-20.86,;53.86,-22.4,;55.2,-23.17,;56.54,-22.4,;55.2,-24.71,;55.2,-20.09,;55.2,-18.55,;56.53,-20.86,;57.86,-20.08,;57.86,-18.54,;59.2,-17.78,;59.2,-16.23,;57.85,-15.46,;60.53,-15.47,;59.2,-20.86,;60.53,-20.09,;59.2,-22.39,)| Show InChI InChI=1S/C87H134N28O22/c1-46(2)36-61(79(130)112-63(39-52-41-99-55-25-13-12-24-53(52)55)80(131)113-64(40-67(92)119)81(132)110-60(85(136)137)30-31-66(91)118)111-77(128)56(26-14-16-32-88)108-76(127)59(29-19-35-98-87(95)96)107-73(124)48(4)104-83(134)65(45-116)114-78(129)57(27-15-17-33-89)109-75(126)58(28-18-34-97-86(93)94)106-72(123)47(3)103-69(121)44-102-84(135)71(49(5)117)115-82(133)62(38-51-22-10-7-11-23-51)105-70(122)43-100-68(120)42-101-74(125)54(90)37-50-20-8-6-9-21-50/h6-13,20-25,41,46-49,54,56-65,71,99,116-117H,14-19,26-40,42-45,88-90H2,1-5H3,(H2,91,118)(H2,92,119)(H,100,120)(H,101,125)(H,102,135)(H,103,121)(H,104,134)(H,105,122)(H,106,123)(H,107,124)(H,108,127)(H,109,126)(H,110,132)(H,111,128)(H,112,130)(H,113,131)(H,114,129)(H,115,133)(H,136,137)(H4,93,94,97)(H4,95,96,98)/t47-,48-,49+,54-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,71-/m0/s1 | PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 50 | n/a | n/a | n/a | n/a |
TBA
Curated by ChEMBL
| Assay Description
Activation of rat ORL1 receptor expressed in african green monkey COS7 cells by [35S]GTPgammaS binding assay |
Bioorg Med Chem 16: 9261-7 (2008)
Article DOI: 10.1016/j.bmc.2008.09.014
BindingDB Entry DOI: 10.7270/Q2MC90XH |
More data for this
Ligand-Target Pair | |
Nociceptin receptor
(RAT) | BDBM50274468
(CHEMBL510117 | FGGFTGARKSARKLWNQ)Show SMILES CC(C)C[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](C)NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccccc1)[C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O |r,wU:91.92,68.68,100.103,59.59,39.44,28.28,8.13,106.107,128.131,wD:72.80,48.55,33.35,17.24,4.4,120.123,(47.19,-24.72,;47.19,-23.18,;48.53,-22.41,;45.85,-22.41,;45.85,-20.87,;44.53,-20.1,;43.18,-20.88,;43.18,-22.41,;41.85,-20.11,;41.85,-18.57,;43.18,-17.79,;43.18,-16.25,;44.52,-15.48,;44.52,-13.94,;40.52,-20.88,;39.19,-20.11,;39.19,-18.56,;37.85,-20.88,;37.85,-22.42,;39.19,-23.19,;39.19,-24.73,;40.53,-25.5,;40.53,-27.04,;39.19,-27.8,;41.86,-27.81,;36.52,-20.12,;35.18,-20.89,;35.18,-22.42,;33.85,-20.11,;33.85,-18.57,;32.52,-20.89,;31.18,-20.12,;31.18,-18.58,;29.85,-20.89,;29.85,-22.43,;31.18,-23.2,;28.52,-20.12,;27.18,-20.89,;27.18,-22.43,;25.85,-20.12,;25.85,-18.58,;27.18,-17.82,;27.18,-16.27,;28.51,-15.5,;28.51,-13.96,;24.51,-20.9,;23.18,-20.13,;23.18,-18.59,;21.84,-20.9,;21.84,-22.43,;23.18,-23.21,;23.18,-24.74,;24.52,-25.52,;24.52,-27.06,;23.18,-27.82,;25.85,-27.83,;20.51,-20.13,;19.17,-20.9,;19.17,-22.44,;17.84,-20.14,;17.84,-18.59,;16.51,-20.91,;15.17,-20.14,;15.17,-18.59,;13.84,-20.91,;12.51,-20.14,;11.17,-20.92,;11.17,-22.45,;9.84,-20.14,;8.5,-20.91,;7.17,-20.15,;7.17,-18.61,;5.84,-20.92,;5.84,-22.46,;7.17,-23.23,;8.5,-22.45,;9.84,-23.22,;9.84,-24.76,;8.51,-25.54,;7.18,-24.76,;4.5,-20.15,;3.17,-20.92,;3.17,-22.46,;1.84,-20.16,;.5,-20.93,;-.84,-20.16,;-.84,-18.62,;-2.16,-20.93,;-3.5,-20.16,;-4.84,-20.93,;-4.84,-22.47,;-6.17,-20.16,;-7.51,-20.93,;-6.17,-18.62,;-4.84,-17.85,;-3.51,-18.62,;-2.17,-17.84,;-2.17,-16.31,;-3.51,-15.54,;-4.84,-16.31,;9.84,-18.6,;8.5,-17.83,;11.17,-17.83,;47.19,-20.1,;47.19,-18.56,;48.52,-20.87,;49.86,-20.1,;49.86,-18.55,;51.19,-17.79,;52.6,-18.41,;53.62,-17.26,;52.86,-15.93,;53.33,-14.46,;52.29,-13.32,;50.79,-13.64,;50.32,-15.11,;51.35,-16.25,;51.19,-20.86,;51.19,-22.4,;52.53,-20.09,;53.86,-20.86,;53.86,-22.4,;55.2,-23.17,;56.54,-22.4,;55.2,-24.71,;55.2,-20.09,;55.2,-18.55,;56.53,-20.86,;57.86,-20.08,;57.86,-18.54,;59.2,-17.78,;59.2,-16.23,;57.85,-15.46,;60.53,-15.47,;59.2,-20.86,;60.53,-20.09,;59.2,-22.39,)| Show InChI InChI=1S/C87H134N28O22/c1-46(2)36-61(79(130)112-63(39-52-41-99-55-25-13-12-24-53(52)55)80(131)113-64(40-67(92)119)81(132)110-60(85(136)137)30-31-66(91)118)111-77(128)56(26-14-16-32-88)108-76(127)59(29-19-35-98-87(95)96)107-73(124)48(4)104-83(134)65(45-116)114-78(129)57(27-15-17-33-89)109-75(126)58(28-18-34-97-86(93)94)106-72(123)47(3)103-69(121)44-102-84(135)71(49(5)117)115-82(133)62(38-51-22-10-7-11-23-51)105-70(122)43-100-68(120)42-101-74(125)54(90)37-50-20-8-6-9-21-50/h6-13,20-25,41,46-49,54,56-65,71,99,116-117H,14-19,26-40,42-45,88-90H2,1-5H3,(H2,91,118)(H2,92,119)(H,100,120)(H,101,125)(H,102,135)(H,103,121)(H,104,134)(H,105,122)(H,106,123)(H,107,124)(H,108,127)(H,109,126)(H,110,132)(H,111,128)(H,112,130)(H,113,131)(H,114,129)(H,115,133)(H,136,137)(H4,93,94,97)(H4,95,96,98)/t47-,48-,49+,54-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,71-/m0/s1 | PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
GoogleScholar
AffyNet
| CHEMBL
KEGG
PC cid
PC sid
UniChem
Similars
| Article
PubMed
| n/a | n/a | n/a | n/a | 50 | n/a | n/a | n/a | n/a |
Kyushu University
Curated by ChEMBL
| Assay Description
Agonist activity at rat ORL1 receptor expressed in african green monkey COS7 cells assessed as stimulation of [35S]GTPgammaS binding by radioligand r... |
Bioorg Med Chem 17: 5683-7 (2009)
Article DOI: 10.1016/j.bmc.2009.06.015
BindingDB Entry DOI: 10.7270/Q2GB2435 |
More data for this
Ligand-Target Pair | |
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