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SMILES: CCOC(=O)\C=C\[C@H](C[C@@H]1CCNC1=O)NC(=O)\C=C\c1ccc(F)c(Br)c1

InChI Key: InChIKey=CTSASDGCROCFDK-DZPAJJIOSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50112652   
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
Genome polyprotein


(Human rhinovirus B)		BDBM50112652
PNG
(4-[3-(3-Bromo-4-fluoro-phenyl)-acryloylamino]-5-(2...)
Show SMILES CCOC(=O)\C=C\[C@H](C[C@@H]1CCNC1=O)NC(=O)\C=C\c1ccc(F)c(Br)c1
Show InChI InChI=1S/C20H22BrFN2O4/c1-2-28-19(26)8-5-15(12-14-9-10-23-20(14)27)24-18(25)7-4-13-3-6-17(22)16(21)11-13/h3-8,11,14-15H,2,9-10,12H2,1H3,(H,23,27)(H,24,25)/b7-4+,8-5+/t14-,15+/m0/s1
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents

Similars
PubMed
n/an/an/an/a 630n/an/an/an/a



Pfizer Global R&D-La Jolla/Agouron Pharmaceuticals

Curated by ChEMBL


Assay Description
Inhibition of Human Rhinovirus 14 (HRV14) Protease 3C

J Med Chem 45: 2016-23 (2002)


BindingDB Entry DOI: 10.7270/Q289156B
More data for this
Ligand-Target Pair