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BDBM50508791 CHEMBL4439382

SMILES: CCn1c2c(Oc3cc(C)cc(C)c3)cccc2[nH]c1=O

InChI Key: InChIKey=DVXVPYYPPJWRIL-UHFFFAOYSA-N

Data: 1 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50508791   
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


(Human immunodeficiency virus 1)
BDBM50508791
PNG
(CHEMBL4439382)
Show SMILES CCn1c2c(Oc3cc(C)cc(C)c3)cccc2[nH]c1=O
Show InChI InChI=1S/C17H18N2O2/c1-4-19-16-14(18-17(19)20)6-5-7-15(16)21-13-9-11(2)8-12(3)10-13/h5-10H,4H2,1-3H3,(H,18,20)
PDB
MMDB

UniProtKB/TrEMBL

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 303n/an/an/an/an/an/a



Stellenbosch University

Curated by ChEMBL


Assay Description
Inhibition of wild-type HIV1 reverse transcriptase in HIV1 infected HEK293T cells harboring luciferase gene assessed as reduction in viral infection ...


ACS Med Chem Lett 10: 196-202 (2019)


Article DOI: 10.1021/acsmedchemlett.8b00549
More data for this
Ligand-Target Pair