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TargetKappa-type opioid receptor
LigandBDBM50369225
Substrate/Competitorn/a
Meas. Tech.ChEMBL_145552
IC50 1.2±n/a nM
Citation Chang ACChao CCTakemori AEGekker GHu SPeterson PKPortoghese PS Arylacetamide-derived fluorescent probes: synthesis, biological evaluation, and direct fluorescent labeling of kappa opioid receptors in mouse microglial cells. J Med Chem 39:1729-35 (1996) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Kappa-type opioid receptor
Name:Kappa-type opioid receptor
Synonyms:KOR-1 | MSL-1 | OPIATE Kappa | OPRK1
Type:Enzyme
Mol. Mass.:42656.78
Organism:Mus musculus (Mouse)
Description:P33534
Residue:380
Sequence:
MESPIQIFRGDPGPTCSPSACLLPNSSSWFPNWAESDSNGSVGSEDQQLESAHISPAIPV
IITAVYSVVFVVGLVGNSLVMFVIIRYTKMKTATNIYIFNLALADALVTTTMPFQSAVYL
MNSWPFGDVLCKIVISIDYYNMFTSIFTLTMMSVDRYIAVCHPVKALDFRTPLKAKIINI
CIWLLASSVGISAIVLGGTKVREDVDVIECSLQFPDDEYSWWDLFMKICVFVFAFVIPVL
IIIVCYTLMILRLKSVRLLSGSREKDRNLRRITKLVLVVVAVFIICWTPIHIFILVEALG
STSHSTAALSSYYFCIALGYTNSSLNPVLYAFLDENFKRCFRDFCFPIKMRMERQSTNRV
RNTVQDPASMRDVGGMNKPV
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  Blast E-value cutoff:
BDBM50369225
n/a
NameBDBM50369225
Synonyms:CHEMBL1907786
TypeSmall organic molecule
Emp. Form.C42H36Cl2N4O6S
Mol. Mass.795.729
SMILESCN([C@H](CN1CCCC1)c1cccc(NC(=S)Nc2ccc(c(c2)C(O)=O)-c2c3ccc(O)cc3oc3cc(=O)ccc23)c1)C(=O)Cc1ccc(Cl)c(Cl)c1 |r,wU:2.1,(9.12,-13.32,;8.28,-12.01,;9.03,-10.64,;10.57,-10.59,;11.38,-11.87,;10.96,-13.34,;12.2,-14.2,;13.44,-13.29,;12.92,-11.83,;8.19,-9.33,;6.65,-9.4,;5.83,-8.11,;6.54,-6.75,;8.07,-6.68,;8.77,-5.29,;10.31,-5.21,;11.15,-6.51,;11.01,-3.83,;12.55,-3.76,;13.39,-5.04,;14.93,-4.95,;15.63,-3.57,;14.8,-2.32,;13.26,-2.39,;15.51,-.91,;17.06,-.82,;14.67,.37,;16.79,-4.62,;16.79,-6.16,;15.44,-6.93,;15.44,-8.47,;16.79,-9.24,;16.79,-10.78,;18.1,-8.47,;18.1,-6.93,;19.45,-6.16,;19.45,-4.62,;20.78,-3.85,;20.78,-2.32,;22.15,-1.52,;19.45,-1.55,;18.1,-2.32,;18.1,-3.85,;8.91,-7.96,;6.75,-12.06,;5.95,-10.78,;6.05,-13.44,;4.51,-13.5,;3.67,-12.2,;2.13,-12.26,;1.41,-13.6,;-.13,-13.64,;2.24,-14.92,;1.52,-16.3,;3.78,-14.86,)|
Structure
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