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TargetGag-Pol polyprotein [489-587]
LigandBDBM50114969
Substrate/Competitorn/a
Meas. Tech.ChEBML_79805
IC50 7740±n/a nM
Citation Murphy, PVO'Brien, JLGorey-Feret, LJSmith, AB Structure-based design and synthesis of HIV-1 protease inhibitors employing beta-D-mannopyranoside scaffolds. Bioorg Med Chem Lett12:1763-6 (2002) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Gag-Pol polyprotein [489-587]
Name:Gag-Pol polyprotein [489-587]
Synonyms:Human immunodeficiency virus type 1 protease | POL_HV1H2 | Pol polyprotein | gag-pol
Type:Enzyme Subunit
Mol. Mass.:10781.16
Organism:Human immunodeficiency virus type 1
Description:P04585[489-587]
Residue:99
Sequence:
PQVTLWQRPLVTIKIGGQLKEALLDTGADDTVLEEMSLPGRWKPKMIGGIGGFIKVRQYD
QILIEICGHKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50114969
n/a
NameBDBM50114969
Synonyms:CHEMBL51564 | N-[(3R,5R,6R)-4-Benzyloxy-5-hydroxy-6-methoxy-3-(4-methoxy-phenoxy)-tetrahydro-pyran-2-ylmethyl]-acetamide
TypeSmall organic molecule
Emp. Form.C23H29NO7
Mol. Mass.431.4789
SMILESCO[C@@H]1OC(CNC(C)=O)[C@@H](Oc2ccc(OC)cc2)C(OCc2ccccc2)[C@H]1O
Structure
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