BDBM50045401 17-Hydroxy-2-methanesulfonyl-10,13-dimethyl-tetradecahydro-20-oxa-cyclopropa[4,5]cyclopenta[a]phenanthren-3-one::CHEMBL3137862
SMILES: [H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@]23OC2C(=O)C(C[C@]13C)S(C)(=O)=O
InChI Key: InChIKey=FELAYLQGNMVPPT-HOARYHOPSA-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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Human immunodeficiency virus type 1 Tat protein (Human immunodeficiency virus type 1 (isolate PCV12...) | BDBM50045401![]() (17-Hydroxy-2-methanesulfonyl-10,13-dimethyl-tetrad...) | PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet ![]() | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 8.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Sterling Winthrop Pharmaceuticals Research Division Curated by ChEMBL | Assay Description Inhibition of HIV-1 nuclear regulatory protein Tat | J Med Chem 36: 2701-2 (1993) BindingDB Entry DOI: 10.7270/Q2NG4PP3 | |||||||||||
More data for this Ligand-Target Pair |