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BDBM50130314 CHEMBL3633040

SMILES: COc1ccccc1Oc1c(NS(=O)(=O)c2ccc(cc2)S(F)(F)(F)(F)F)cc(cc1OCCO)-c1ncccn1

InChI Key: InChIKey=OUWVSODMIMINEM-UHFFFAOYSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50130314   
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
Endothelin-1 receptor


(Homo sapiens (Human))
BDBM50130314
PNG
(CHEMBL3633040)
Show SMILES COc1ccccc1Oc1c(NS(=O)(=O)c2ccc(cc2)S(F)(F)(F)(F)F)cc(cc1OCCO)-c1ncccn1
Show InChI InChI=1S/C25H22F5N3O6S2/c1-37-21-5-2-3-6-22(21)39-24-20(15-17(16-23(24)38-14-13-34)25-31-11-4-12-32-25)33-40(35,36)18-7-9-19(10-8-18)41(26,27,28,29)30/h2-12,15-16,33-34H,13-14H2,1H3
UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
PubMed
n/an/a 112n/an/an/an/an/an/a



Bristol-Myers Squibb Research and Development

Curated by ChEMBL


Assay Description
Antagonist activity at human ETA receptor expressed in CHO cells assessed as inhibition of ET-1-induced Ca2+ efflux from endoplasmic reticulum into c...


J Med Chem 58: 8315-59 (2015)


BindingDB Entry DOI: 10.7270/Q22J6DPZ
More data for this
Ligand-Target Pair