Reaction Details Report a problem with these data
Target
Integrase
Ligand
BDBM506
Substrate
n/a
Meas. Tech.
ChEMBL_88776 (CHEMBL701807)
IC50
1000±n/a nM
Citation
 Mazumder, A; Wang, S; Neamati, N; Nicklaus, M; Sunder, S; Chen, J; Milne, GW; Rice, WG; Burke, TR; Pommier, Y Antiretroviral agents as inhibitors of both human immunodeficiency virus type 1 integrase and protease. J Med Chem 39:2472-81 (1996) [PubMed]  Article 
Target
Name:
Integrase
Synonyms:
Human immunodeficiency virus type 2 integrase
Type:
PROTEIN
Mol. Mass.:
10781.73
Organism:
Human immunodeficiency virus 2
Description:
ChEMBL_88781
Residue:
95
Sequence:
IPQETGRQTALFLLKLASRWPITHLHTDNGSNFTSQEVKMVAWWIGIEQSFGVPYNPQSQGVVEAMNHHLKNQISRIREQANTVETIVLVAVHCM
  
Inhibitor
Name:
BDBM506
Synonyms:
3-({4-[bis(4-hydroxy-2-oxo-2H-chromen-3-yl)methyl]phenyl}(4-hydroxy-2-oxo-2H-chromen-3-yl)methyl)-4-hydroxy-2H-chromen-2-one | CHEMBL293914 | Cancer Chemotherapy National Service Center (CCNSC) compound 158393 | NSC 158393
Type:
Small organic molecule
Emp. Form.:
C44H26O12
Mol. Mass.:
746.67
SMILES:
Oc1c(C(c2ccc(cc2)C(c2c(O)c3ccccc3oc2=O)c2c(O)c3ccccc3oc2=O)c2c(O)c3ccccc3oc2=O)c(=O)oc2ccccc12
Structure:
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