BDBM3139 2-pyridinone deriv. 45::5-ethyl-3-{[(3-methoxypyridin-2-yl)methyl]amino}-6-methyl-1,2-dihydropyridin-2-one
SMILES: CCc1cc(NCc2ncccc2OC)c(=O)[nH]c1C
InChI Key: InChIKey=KFBVWLLJEARXPV-UHFFFAOYSA-N
Data: 1 IC50
Target/Host (Institution) | Ligand | Target/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 | pH | Temp °C |
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HIV-1 Reverse Transcriptase (Human immunodeficiency virus type 1) | BDBM3139![]() (2-pyridinone deriv. 45 | 5-ethyl-3-{[(3-methoxypyr...) | PDB MMDB B.MOAD GoogleScholar AffyNet ![]() | PC cid PC sid UniChem Similars | Article PubMed | n/a | n/a | 1.55E+3 | n/a | n/a | n/a | n/a | 8.2 | n/a |
Merck Research Laboratories | Assay Description The IC50 of reverse transcriptase is the concentration that inhibits 50% of recombinant HIV-1 RT RNA-directed DNA polymerase activity in vitro. | J Med Chem 36: 249-55 (1993) Article DOI: 10.1021/jm00054a009 BindingDB Entry DOI: 10.7270/Q20863HM | |||||||||||
More data for this Ligand-Target Pair |