Target
Integrase
Ligand
BDBM50477465
Substrate
n/a
Meas. Tech.
ChEMBL_455147 (CHEMBL887177)
IC50
20000±n/a nM
Citation
 Sriram, DYogeeswari, PSenchani, GBanerjee, D Newer tetracycline derivatives: synthesis, anti-HIV, antimycobacterial activities and inhibition of HIV-1 integrase. Bioorg Med Chem Lett 17:2372-5 (2007) [PubMed]  Article
Target
Name:
Integrase
Synonyms:
pol
Type:
PROTEIN
Mol. Mass.:
32203.43
Organism:
Human immunodeficiency virus 1
Description:
ChEMBL_106649
Residue:
288
Sequence:
FLDGIDKAQEEHEKYHSNWRAMASDFNLPPVVAKEIVASCDKCQLKGEAMHGQVDCSPGIWQLDCTHLEGKVILVAVHVASGYIEAEVIPAETGQETAYFLLKLAGRWPVKTVHTDNGSNFTSTTVKAACWWAGIKQEFGIPYNPQSQGVIESMNKELKKIIGQVRDQAEHLKTAVQMAVFIHNFKRKGGIGGYSAGERIVDIIATDIQTKELQKQITKIQNFRVYYRDSRDPVWKGPAKLLWKGEGAVVIQDNSDIKVVPRRKAKIIRDYGKQMAGDDCVASRQDED
  
Inhibitor
Name:
BDBM50477465
Synonyms:
CHEMBL239177
Type:
Small organic molecule
Emp. Form.:
C41H46F2N6O10
Mol. Mass.:
820.8349
SMILES:
[H][C@@]12Cc3c(ccc(O)c3C(=O)C1=C(O)[C@]1(O)C(=O)C(C(=O)NCN3CCN(CC3C)c3c(F)cc4c(c3F)n(CC)cc(C(O)=O)c4=O)=C(O)[C@@H](N(C)C)[C@]1([H])C2)N(C)C |t:14,53|
Structure:
Search PDB for entries with ligand similarity: