Target/Host (Institution) | Ligand | Target/Host Links | Ligand Links | Trg + Lig Links | Ki nM | ΔG° kJ/mole | IC50 nM | Kd nM | EC50/IC50 nM | koff s-1 | kon M-1s-1 | pH | Temp °C |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Protein Tat (Human immunodeficiency virus type 1 (isolate PCV12...) | BDBM50045400 (Acetic acid 2-methanesulfonyl-10,13-dimethyl-3-oxo...) | PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 2.60E+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 | |||||||||||||
Protein Tat (Human immunodeficiency virus type 1 (isolate PCV12...) | BDBM50045403 (Acetic acid 2-carbamoyl-3-hydroxy-10,13-dimethyl-1...) | PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 2.60E+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 | |||||||||||||
Protein Tat (Human immunodeficiency virus type 1 (isolate PCV12...) | BDBM50032828 (7-Chloro-5-(1H-pyrrol-2-yl)-1,3-dihydro-benzo[e][1...) | PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | Purchase CHEMBL MCE PC cid PC sid UniChem Patents | PubMed | n/a | n/a | 4.00E+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 | |||||||||||||
Protein Tat (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 | |||||||||||||
Protein Tat (Human immunodeficiency virus type 1 (isolate PCV12...) | BDBM50045402 (3,17-Dihydroxy-10,13-dimethyl-1,4,6,7,8,9,10,11,12...) | PDB MMDB Reactome pathway UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 1.43E+4 | 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 |