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SMILES: Cc1c(Sc2ccccc2)n(C\C=C\c2ccccc2)c(=O)[nH]c1=O

InChI Key: InChIKey=DJYIGLXJQVOCGM-DHZHZOJOSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50058304   
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)
BDBM50058304
PNG
(5-Methyl-1-((E)-3-phenyl-allyl)-6-phenylsulfanyl-1...)
Show SMILES Cc1c(Sc2ccccc2)n(C\C=C\c2ccccc2)c(=O)[nH]c1=O
Show InChI InChI=1S/C20H18N2O2S/c1-15-18(23)21-20(24)22(14-8-11-16-9-4-2-5-10-16)19(15)25-17-12-6-3-7-13-17/h2-13H,14H2,1H3,(H,21,23,24)/b11-8+
PDB
MMDB

UniProtKB/TrEMBL

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

Similars

Article
PubMed
n/an/an/an/a 2.50E+3n/an/an/an/a



Université d'Orléans

Curated by ChEMBL


Assay Description
Inhibitory concentration against HIV-1 reverse transcriptase


J Med Chem 40: 4257-64 (1998)


Article DOI: 10.1021/jm970110p
BindingDB Entry DOI: 10.7270/Q2WS8SC3
More data for this
Ligand-Target Pair