BDBM2273 2-Pyridinone derivative 53::3-[2-(1,3-benzoxazol-2-yl)ethyl]-5-(methoxymethyl)-6-methyl-1,2-dihydropyridin-2-one::3-[2-(Benzoxazol-2-yl)ethyl]-5-(methoxymethyl)-6-methylpyridin-2(1H)-one::CHEMBL177174
SMILES: COCc1cc(CCc2nc3ccccc3o2)c(=O)[nH]c1C
InChI Key: InChIKey=VBVSFIQZDYOTQA-UHFFFAOYSA-N
Data: 2 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Human immunodeficiency virus type 1 reverse transcriptase (Human immunodeficiency virus 1) | BDBM2273 (2-Pyridinone derivative 53 | 3-[2-(1,3-benzoxazol-...) | PDB MMDB UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 2.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Reserch Laboratories Curated by ChEMBL | Assay Description Tested for inhibition against HIV-1 RT (used (poly)rC-(oligo)dG as the template) | J Med Chem 36: 953-66 (1993) BindingDB Entry DOI: 10.7270/Q2JW8G28 | |||||||||||
More data for this Ligand-Target Pair | |||||||||||||
HIV-1 Reverse Transcriptase (Human immunodeficiency virus type 1) | BDBM2273 (2-Pyridinone derivative 53 | 3-[2-(1,3-benzoxazol-...) | PDB MMDB B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 2.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Merck Reserch Laboratories Curated by ChEMBL | 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: 953-66 (1993) BindingDB Entry DOI: 10.7270/Q2JW8G28 | |||||||||||
More data for this Ligand-Target Pair |