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SMILES: COC(=O)CCC\C=C(\c1cc(Cl)c(OC)c(c1)C(=O)OC)c1cc(Cl)ccc1OC

InChI Key: InChIKey=GVYHWCSTRPXJKQ-APSNUPSMSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50173807   
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
Reverse transcriptase/RNaseH


(Human immunodeficiency virus 1)
BDBM50173807
PNG
(3-Chloro-5-[(Z)-1-(5-chloro-2-methoxy-phenyl)-5-me...)
Show SMILES COC(=O)CCC\C=C(\c1cc(Cl)c(OC)c(c1)C(=O)OC)c1cc(Cl)ccc1OC
Show InChI InChI=1S/C23H24Cl2O6/c1-28-20-10-9-15(24)13-17(20)16(7-5-6-8-21(26)29-2)14-11-18(23(27)31-4)22(30-3)19(25)12-14/h7,9-13H,5-6,8H2,1-4H3/b16-7-
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
DrugBank
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



Purdue University

Curated by ChEMBL


Assay Description
Inhibition of recombinant HIV-1 reverse transcriptase activity


J Med Chem 48: 6140-55 (2005)


Article DOI: 10.1021/jm050452s
BindingDB Entry DOI: 10.7270/Q2TB16F6
More data for this
Ligand-Target Pair