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SMILES: OC(=O)[C@H](Cc1cccs1)NC(=O)c1ccccc1Br

InChI Key: InChIKey=HWNCRYGEVNLQTM-LBPRGKRZSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50125198   
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
Integrin alpha-L/Integrin beta-2/Intercellular adhesion molecule 1


(Homo sapiens (Human))
BDBM50125198
PNG
((S)-2-(2-Bromo-benzoylamino)-3-thiophen-2-yl-propi...)
Show SMILES OC(=O)[C@H](Cc1cccs1)NC(=O)c1ccccc1Br
Show InChI InChI=1S/C14H12BrNO3S/c15-11-6-2-1-5-10(11)13(17)16-12(14(18)19)8-9-4-3-7-20-9/h1-7,12H,8H2,(H,16,17)(H,18,19)/t12-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
antibodypedia
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
PubMed
n/an/a 5.50E+3n/an/an/an/an/an/a



Genentech

Curated by ChEMBL


Assay Description
In vitro inhibitory potency for preventing sarafotoxin S6c induced constriction of rat tracheal rings (ETB receptor)


Bioorg Med Chem Lett 13: 1015-8 (2003)


BindingDB Entry DOI: 10.7270/Q2K35V6V
More data for this
Ligand-Target Pair