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TargetKappa-type opioid receptor
LigandBDBM50018728
Substrate/Competitorn/a
Meas. Tech.ChEMBL_146515 (CHEMBL754624)
Ki 61±n/a nM
Citation Zimmerman, DMCantrell, BESwartzendruber, JKJones, NDMendelsohn, LGLeander, JDNickander, RC Synthesis and analgesic properties of N-substituted trans-4a-aryldecahydroisoquinolines. J Med Chem31:555-60 (1988) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Kappa-type opioid receptor
Name:Kappa-type opioid receptor
Synonyms:Kappa Opioid Receptor | OPIATE Kappa | OPRK1 | OPRK_CAVPO | Opiate Kappa 1 | mu/kappa opioid receptor
Type:G Protein-Coupled Receptor (GPCR)
Mol. Mass.:42744.99
Organism:Cavia porcellus (domestic guinea pig)
Description:P41144
Residue:380
Sequence:
MGRRRQGPAQPASELPARNACLLPNGSAWLPGWAEPDGNGSAGPQDEQLEPAHISPAIPV
IITAVYSVVFVVGLVGNSLVMFVIIRYTKMKTATNIYIFNLALADALVTTTMPFQSTVYL
MNSWPFGDVLCKIVISIDYYNMFTSIFTLTMMSVDRYIAVCHPVKALDFRTPLKAKIINI
CIWLLSSSVGISAIILGGTKVREDVDIIECSLQFPDDDYSWWDLFMKICVFVFAFVIPVL
IIIVCYTLMILRLKSVRLLSGSREKDRNLRRITRLVLVVVAVFIICWTPIHIFILVEALG
STSHSTAALSSYYFCIALGYTNSSLNPILYAFLDENFKRCFRDFCFPIKMRMERQSTSRV
RNTVQDPAYMRNVDGVNKPV
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  Blast E-value cutoff:
BDBM50018728
n/a
NameBDBM50018728
Synonyms:3-(2-Methyl-octahydro-isoquinolin-4a-yl)-phenol | CHEMBL155216
TypeSmall organic molecule
Emp. Form.C16H23NO
Mol. Mass.245.3599
SMILESCN1CCC2(CCCC[C@H]2C1)c1cccc(O)c1
Structure
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