BindingDB logo
myBDB logout

null

SMILES: C[C@@H](O)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccccc1)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O

InChI Key: InChIKey=MRPJNGQFWWZSQY-FMCSKRGOSA-N

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 4 hits for monomerid = 50274461   
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
Nociceptin receptor


(RAT)
BDBM50274461
PNG
(CHEMBL504587 | FGGFTGARKSARKWANQ)
Show SMILES C[C@@H](O)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccccc1)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O |r,wU:26.27,3.3,1.1,42.44,58.59,73.75,89.90,112.116,125.128,wD:7.15,47.48,67.68,78.79,98.99,117.120,(9.16,.66,;10.48,-.11,;11.83,.66,;10.48,-1.65,;9.16,-2.42,;7.82,-1.64,;7.82,-.1,;6.49,-2.41,;6.49,-3.95,;7.82,-4.73,;9.15,-3.96,;10.49,-4.73,;10.48,-6.27,;9.15,-7.04,;7.81,-6.27,;5.15,-1.64,;3.82,-2.41,;3.82,-3.95,;2.48,-1.64,;1.15,-2.4,;-.19,-1.63,;-.19,-.09,;-1.52,-2.4,;-2.86,-1.63,;-4.19,-2.4,;-4.19,-3.94,;-5.52,-1.63,;-6.86,-2.4,;-5.52,-.09,;-4.2,.69,;-2.86,-.09,;-1.52,.68,;-1.52,2.22,;-2.85,2.99,;-4.19,2.22,;11.83,-2.42,;11.83,-3.96,;13.16,-1.65,;14.49,-2.42,;15.82,-1.66,;15.82,-.12,;17.16,-2.43,;18.5,-1.65,;18.5,-.12,;19.83,-2.43,;19.83,-3.97,;21.16,-1.66,;22.5,-2.43,;22.5,-3.98,;23.83,-4.74,;23.83,-6.29,;25.16,-7.06,;25.16,-8.61,;23.83,-9.38,;26.5,-9.37,;23.83,-1.66,;23.83,-.12,;25.17,-2.43,;26.5,-1.67,;26.5,-.13,;27.84,.64,;27.84,2.18,;29.18,2.95,;29.18,4.49,;27.84,-2.44,;27.84,-3.98,;29.17,-1.67,;30.51,-2.44,;30.51,-3.98,;31.84,-4.76,;31.84,-1.67,;31.84,-.13,;33.18,-2.45,;34.51,-1.68,;34.51,-.14,;35.85,-2.45,;35.85,-4,;37.18,-1.68,;38.52,-2.45,;38.52,-4,;39.85,-4.77,;39.85,-6.31,;41.18,-7.08,;41.18,-8.62,;39.84,-9.4,;42.52,-9.39,;39.85,-1.69,;39.85,-.15,;41.19,-2.46,;42.52,-1.69,;42.52,-.15,;43.85,.63,;43.85,2.16,;45.19,2.94,;45.19,4.47,;43.85,-2.46,;43.85,-4,;45.19,-1.69,;46.53,-2.47,;46.53,-4.01,;47.86,-4.77,;49.26,-4.15,;50.29,-5.3,;49.52,-6.63,;49.99,-8.1,;48.96,-9.24,;47.45,-8.92,;46.98,-7.45,;48.02,-6.31,;47.86,-1.69,;47.86,-.15,;49.19,-2.46,;50.53,-1.7,;50.53,-.16,;51.86,-2.47,;51.86,-4.02,;53.19,-1.7,;54.53,-2.47,;54.53,-4.01,;55.87,-4.79,;57.2,-4.01,;55.87,-6.33,;55.87,-1.7,;55.87,-.17,;57.21,-2.48,;58.53,-1.71,;58.53,-.17,;59.87,.6,;59.87,2.14,;58.54,2.91,;61.21,2.91,;59.87,-2.48,;61.2,-1.71,;59.87,-4.02,)|
Show InChI InChI=1S/C84H128N28O22/c1-44(100-66(118)42-99-81(132)68(47(4)114)112-79(130)59(36-49-21-9-6-10-22-49)103-67(119)41-97-65(117)40-98-72(123)52(87)35-48-19-7-5-8-20-48)69(120)104-56(27-17-33-94-83(90)91)73(124)107-55(26-14-16-32-86)76(127)111-62(43-113)80(131)102-45(2)70(121)105-57(28-18-34-95-84(92)93)74(125)106-54(25-13-15-31-85)75(126)110-60(37-50-39-96-53-24-12-11-23-51(50)53)77(128)101-46(3)71(122)109-61(38-64(89)116)78(129)108-58(82(133)134)29-30-63(88)115/h5-12,19-24,39,44-47,52,54-62,68,96,113-114H,13-18,25-38,40-43,85-87H2,1-4H3,(H2,88,115)(H2,89,116)(H,97,117)(H,98,123)(H,99,132)(H,100,118)(H,101,128)(H,102,131)(H,103,119)(H,104,120)(H,105,121)(H,106,125)(H,107,124)(H,108,129)(H,109,122)(H,110,126)(H,111,127)(H,112,130)(H,133,134)(H4,90,91,94)(H4,92,93,95)/t44-,45-,46-,47+,52-,54-,55-,56-,57-,58-,59-,60-,61-,62-,68-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 0.410n/an/an/an/an/an/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)
BDBM50274461
PNG
(CHEMBL504587 | FGGFTGARKSARKWANQ)
Show SMILES C[C@@H](O)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccccc1)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O |r,wU:26.27,3.3,1.1,42.44,58.59,73.75,89.90,112.116,125.128,wD:7.15,47.48,67.68,78.79,98.99,117.120,(9.16,.66,;10.48,-.11,;11.83,.66,;10.48,-1.65,;9.16,-2.42,;7.82,-1.64,;7.82,-.1,;6.49,-2.41,;6.49,-3.95,;7.82,-4.73,;9.15,-3.96,;10.49,-4.73,;10.48,-6.27,;9.15,-7.04,;7.81,-6.27,;5.15,-1.64,;3.82,-2.41,;3.82,-3.95,;2.48,-1.64,;1.15,-2.4,;-.19,-1.63,;-.19,-.09,;-1.52,-2.4,;-2.86,-1.63,;-4.19,-2.4,;-4.19,-3.94,;-5.52,-1.63,;-6.86,-2.4,;-5.52,-.09,;-4.2,.69,;-2.86,-.09,;-1.52,.68,;-1.52,2.22,;-2.85,2.99,;-4.19,2.22,;11.83,-2.42,;11.83,-3.96,;13.16,-1.65,;14.49,-2.42,;15.82,-1.66,;15.82,-.12,;17.16,-2.43,;18.5,-1.65,;18.5,-.12,;19.83,-2.43,;19.83,-3.97,;21.16,-1.66,;22.5,-2.43,;22.5,-3.98,;23.83,-4.74,;23.83,-6.29,;25.16,-7.06,;25.16,-8.61,;23.83,-9.38,;26.5,-9.37,;23.83,-1.66,;23.83,-.12,;25.17,-2.43,;26.5,-1.67,;26.5,-.13,;27.84,.64,;27.84,2.18,;29.18,2.95,;29.18,4.49,;27.84,-2.44,;27.84,-3.98,;29.17,-1.67,;30.51,-2.44,;30.51,-3.98,;31.84,-4.76,;31.84,-1.67,;31.84,-.13,;33.18,-2.45,;34.51,-1.68,;34.51,-.14,;35.85,-2.45,;35.85,-4,;37.18,-1.68,;38.52,-2.45,;38.52,-4,;39.85,-4.77,;39.85,-6.31,;41.18,-7.08,;41.18,-8.62,;39.84,-9.4,;42.52,-9.39,;39.85,-1.69,;39.85,-.15,;41.19,-2.46,;42.52,-1.69,;42.52,-.15,;43.85,.63,;43.85,2.16,;45.19,2.94,;45.19,4.47,;43.85,-2.46,;43.85,-4,;45.19,-1.69,;46.53,-2.47,;46.53,-4.01,;47.86,-4.77,;49.26,-4.15,;50.29,-5.3,;49.52,-6.63,;49.99,-8.1,;48.96,-9.24,;47.45,-8.92,;46.98,-7.45,;48.02,-6.31,;47.86,-1.69,;47.86,-.15,;49.19,-2.46,;50.53,-1.7,;50.53,-.16,;51.86,-2.47,;51.86,-4.02,;53.19,-1.7,;54.53,-2.47,;54.53,-4.01,;55.87,-4.79,;57.2,-4.01,;55.87,-6.33,;55.87,-1.7,;55.87,-.17,;57.21,-2.48,;58.53,-1.71,;58.53,-.17,;59.87,.6,;59.87,2.14,;58.54,2.91,;61.21,2.91,;59.87,-2.48,;61.2,-1.71,;59.87,-4.02,)|
Show InChI InChI=1S/C84H128N28O22/c1-44(100-66(118)42-99-81(132)68(47(4)114)112-79(130)59(36-49-21-9-6-10-22-49)103-67(119)41-97-65(117)40-98-72(123)52(87)35-48-19-7-5-8-20-48)69(120)104-56(27-17-33-94-83(90)91)73(124)107-55(26-14-16-32-86)76(127)111-62(43-113)80(131)102-45(2)70(121)105-57(28-18-34-95-84(92)93)74(125)106-54(25-13-15-31-85)75(126)110-60(37-50-39-96-53-24-12-11-23-51(50)53)77(128)101-46(3)71(122)109-61(38-64(89)116)78(129)108-58(82(133)134)29-30-63(88)115/h5-12,19-24,39,44-47,52,54-62,68,96,113-114H,13-18,25-38,40-43,85-87H2,1-4H3,(H2,88,115)(H2,89,116)(H,97,117)(H,98,123)(H,99,132)(H,100,118)(H,101,128)(H,102,131)(H,103,119)(H,104,120)(H,105,121)(H,106,125)(H,107,124)(H,108,129)(H,109,122)(H,110,126)(H,111,127)(H,112,130)(H,133,134)(H4,90,91,94)(H4,92,93,95)/t44-,45-,46-,47+,52-,54-,55-,56-,57-,58-,59-,60-,61-,62-,68-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 5.80n/an/an/an/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)
BDBM50274461
PNG
(CHEMBL504587 | FGGFTGARKSARKWANQ)
Show SMILES C[C@@H](O)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccccc1)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O |r,wU:26.27,3.3,1.1,42.44,58.59,73.75,89.90,112.116,125.128,wD:7.15,47.48,67.68,78.79,98.99,117.120,(9.16,.66,;10.48,-.11,;11.83,.66,;10.48,-1.65,;9.16,-2.42,;7.82,-1.64,;7.82,-.1,;6.49,-2.41,;6.49,-3.95,;7.82,-4.73,;9.15,-3.96,;10.49,-4.73,;10.48,-6.27,;9.15,-7.04,;7.81,-6.27,;5.15,-1.64,;3.82,-2.41,;3.82,-3.95,;2.48,-1.64,;1.15,-2.4,;-.19,-1.63,;-.19,-.09,;-1.52,-2.4,;-2.86,-1.63,;-4.19,-2.4,;-4.19,-3.94,;-5.52,-1.63,;-6.86,-2.4,;-5.52,-.09,;-4.2,.69,;-2.86,-.09,;-1.52,.68,;-1.52,2.22,;-2.85,2.99,;-4.19,2.22,;11.83,-2.42,;11.83,-3.96,;13.16,-1.65,;14.49,-2.42,;15.82,-1.66,;15.82,-.12,;17.16,-2.43,;18.5,-1.65,;18.5,-.12,;19.83,-2.43,;19.83,-3.97,;21.16,-1.66,;22.5,-2.43,;22.5,-3.98,;23.83,-4.74,;23.83,-6.29,;25.16,-7.06,;25.16,-8.61,;23.83,-9.38,;26.5,-9.37,;23.83,-1.66,;23.83,-.12,;25.17,-2.43,;26.5,-1.67,;26.5,-.13,;27.84,.64,;27.84,2.18,;29.18,2.95,;29.18,4.49,;27.84,-2.44,;27.84,-3.98,;29.17,-1.67,;30.51,-2.44,;30.51,-3.98,;31.84,-4.76,;31.84,-1.67,;31.84,-.13,;33.18,-2.45,;34.51,-1.68,;34.51,-.14,;35.85,-2.45,;35.85,-4,;37.18,-1.68,;38.52,-2.45,;38.52,-4,;39.85,-4.77,;39.85,-6.31,;41.18,-7.08,;41.18,-8.62,;39.84,-9.4,;42.52,-9.39,;39.85,-1.69,;39.85,-.15,;41.19,-2.46,;42.52,-1.69,;42.52,-.15,;43.85,.63,;43.85,2.16,;45.19,2.94,;45.19,4.47,;43.85,-2.46,;43.85,-4,;45.19,-1.69,;46.53,-2.47,;46.53,-4.01,;47.86,-4.77,;49.26,-4.15,;50.29,-5.3,;49.52,-6.63,;49.99,-8.1,;48.96,-9.24,;47.45,-8.92,;46.98,-7.45,;48.02,-6.31,;47.86,-1.69,;47.86,-.15,;49.19,-2.46,;50.53,-1.7,;50.53,-.16,;51.86,-2.47,;51.86,-4.02,;53.19,-1.7,;54.53,-2.47,;54.53,-4.01,;55.87,-4.79,;57.2,-4.01,;55.87,-6.33,;55.87,-1.7,;55.87,-.17,;57.21,-2.48,;58.53,-1.71,;58.53,-.17,;59.87,.6,;59.87,2.14,;58.54,2.91,;61.21,2.91,;59.87,-2.48,;61.2,-1.71,;59.87,-4.02,)|
Show InChI InChI=1S/C84H128N28O22/c1-44(100-66(118)42-99-81(132)68(47(4)114)112-79(130)59(36-49-21-9-6-10-22-49)103-67(119)41-97-65(117)40-98-72(123)52(87)35-48-19-7-5-8-20-48)69(120)104-56(27-17-33-94-83(90)91)73(124)107-55(26-14-16-32-86)76(127)111-62(43-113)80(131)102-45(2)70(121)105-57(28-18-34-95-84(92)93)74(125)106-54(25-13-15-31-85)75(126)110-60(37-50-39-96-53-24-12-11-23-51(50)53)77(128)101-46(3)71(122)109-61(38-64(89)116)78(129)108-58(82(133)134)29-30-63(88)115/h5-12,19-24,39,44-47,52,54-62,68,96,113-114H,13-18,25-38,40-43,85-87H2,1-4H3,(H2,88,115)(H2,89,116)(H,97,117)(H,98,123)(H,99,132)(H,100,118)(H,101,128)(H,102,131)(H,103,119)(H,104,120)(H,105,121)(H,106,125)(H,107,124)(H,108,129)(H,109,122)(H,110,126)(H,111,127)(H,112,130)(H,133,134)(H4,90,91,94)(H4,92,93,95)/t44-,45-,46-,47+,52-,54-,55-,56-,57-,58-,59-,60-,61-,62-,68-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 0.410n/an/an/an/an/an/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)
BDBM50274461
PNG
(CHEMBL504587 | FGGFTGARKSARKWANQ)
Show SMILES C[C@@H](O)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)CNC(=O)[C@@H](N)Cc1ccccc1)C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O |r,wU:26.27,3.3,1.1,42.44,58.59,73.75,89.90,112.116,125.128,wD:7.15,47.48,67.68,78.79,98.99,117.120,(9.16,.66,;10.48,-.11,;11.83,.66,;10.48,-1.65,;9.16,-2.42,;7.82,-1.64,;7.82,-.1,;6.49,-2.41,;6.49,-3.95,;7.82,-4.73,;9.15,-3.96,;10.49,-4.73,;10.48,-6.27,;9.15,-7.04,;7.81,-6.27,;5.15,-1.64,;3.82,-2.41,;3.82,-3.95,;2.48,-1.64,;1.15,-2.4,;-.19,-1.63,;-.19,-.09,;-1.52,-2.4,;-2.86,-1.63,;-4.19,-2.4,;-4.19,-3.94,;-5.52,-1.63,;-6.86,-2.4,;-5.52,-.09,;-4.2,.69,;-2.86,-.09,;-1.52,.68,;-1.52,2.22,;-2.85,2.99,;-4.19,2.22,;11.83,-2.42,;11.83,-3.96,;13.16,-1.65,;14.49,-2.42,;15.82,-1.66,;15.82,-.12,;17.16,-2.43,;18.5,-1.65,;18.5,-.12,;19.83,-2.43,;19.83,-3.97,;21.16,-1.66,;22.5,-2.43,;22.5,-3.98,;23.83,-4.74,;23.83,-6.29,;25.16,-7.06,;25.16,-8.61,;23.83,-9.38,;26.5,-9.37,;23.83,-1.66,;23.83,-.12,;25.17,-2.43,;26.5,-1.67,;26.5,-.13,;27.84,.64,;27.84,2.18,;29.18,2.95,;29.18,4.49,;27.84,-2.44,;27.84,-3.98,;29.17,-1.67,;30.51,-2.44,;30.51,-3.98,;31.84,-4.76,;31.84,-1.67,;31.84,-.13,;33.18,-2.45,;34.51,-1.68,;34.51,-.14,;35.85,-2.45,;35.85,-4,;37.18,-1.68,;38.52,-2.45,;38.52,-4,;39.85,-4.77,;39.85,-6.31,;41.18,-7.08,;41.18,-8.62,;39.84,-9.4,;42.52,-9.39,;39.85,-1.69,;39.85,-.15,;41.19,-2.46,;42.52,-1.69,;42.52,-.15,;43.85,.63,;43.85,2.16,;45.19,2.94,;45.19,4.47,;43.85,-2.46,;43.85,-4,;45.19,-1.69,;46.53,-2.47,;46.53,-4.01,;47.86,-4.77,;49.26,-4.15,;50.29,-5.3,;49.52,-6.63,;49.99,-8.1,;48.96,-9.24,;47.45,-8.92,;46.98,-7.45,;48.02,-6.31,;47.86,-1.69,;47.86,-.15,;49.19,-2.46,;50.53,-1.7,;50.53,-.16,;51.86,-2.47,;51.86,-4.02,;53.19,-1.7,;54.53,-2.47,;54.53,-4.01,;55.87,-4.79,;57.2,-4.01,;55.87,-6.33,;55.87,-1.7,;55.87,-.17,;57.21,-2.48,;58.53,-1.71,;58.53,-.17,;59.87,.6,;59.87,2.14,;58.54,2.91,;61.21,2.91,;59.87,-2.48,;61.2,-1.71,;59.87,-4.02,)|
Show InChI InChI=1S/C84H128N28O22/c1-44(100-66(118)42-99-81(132)68(47(4)114)112-79(130)59(36-49-21-9-6-10-22-49)103-67(119)41-97-65(117)40-98-72(123)52(87)35-48-19-7-5-8-20-48)69(120)104-56(27-17-33-94-83(90)91)73(124)107-55(26-14-16-32-86)76(127)111-62(43-113)80(131)102-45(2)70(121)105-57(28-18-34-95-84(92)93)74(125)106-54(25-13-15-31-85)75(126)110-60(37-50-39-96-53-24-12-11-23-51(50)53)77(128)101-46(3)71(122)109-61(38-64(89)116)78(129)108-58(82(133)134)29-30-63(88)115/h5-12,19-24,39,44-47,52,54-62,68,96,113-114H,13-18,25-38,40-43,85-87H2,1-4H3,(H2,88,115)(H2,89,116)(H,97,117)(H,98,123)(H,99,132)(H,100,118)(H,101,128)(H,102,131)(H,103,119)(H,104,120)(H,105,121)(H,106,125)(H,107,124)(H,108,129)(H,109,122)(H,110,126)(H,111,127)(H,112,130)(H,133,134)(H4,90,91,94)(H4,92,93,95)/t44-,45-,46-,47+,52-,54-,55-,56-,57-,58-,59-,60-,61-,62-,68-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 5.80n/an/an/an/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