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BDBM50123923 CHEMBL164503::Phenyl-(3,4,5-trimethoxy-benzoyl)-thiocarbamic acid O-(2-phenoxy-ethyl) ester

SMILES: COc1cc(cc(OC)c1OC)C(=O)N(C(=S)OCCOc1ccccc1)c1ccccc1

InChI Key: InChIKey=YKTKIEINEATXQJ-UHFFFAOYSA-N

Data: 1 EC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50123923   
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
Human immunodeficiency virus type 1 reverse transcriptase


(Human immunodeficiency virus 1)
BDBM50123923
PNG
(CHEMBL164503 | Phenyl-(3,4,5-trimethoxy-benzoyl)-t...)
Show SMILES COc1cc(cc(OC)c1OC)C(=O)N(C(=S)OCCOc1ccccc1)c1ccccc1
Show InChI InChI=1S/C25H25NO6S/c1-28-21-16-18(17-22(29-2)23(21)30-3)24(27)26(19-10-6-4-7-11-19)25(33)32-15-14-31-20-12-8-5-9-13-20/h4-13,16-17H,14-15H2,1-3H3
PDB
MMDB

UniProtKB/TrEMBL

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

Similars

Article
PubMed
n/an/an/an/a 9.60E+3n/an/an/an/a



Università di Genova

Curated by ChEMBL


Assay Description
Concentration required to achieve 50% protection of MT-4 cell from the HIV-1 induced cytopathogenicity was determined by the MTT method


J Med Chem 46: 768-81 (2003)


Article DOI: 10.1021/jm0209984
BindingDB Entry DOI: 10.7270/Q2BC3XXX
More data for this
Ligand-Target Pair