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TargetHuman immunodeficiency virus type 1 protease
LigandBDBM50291055
Substrate/Competitorn/a
Meas. Tech.ChEBML_157558
Ki 0.860000±n/a nM
Citation Schwartz TMBundy GLStrohbach JWThaisrivongs SJohnson PDSkulnick HITomich PKLynn JCChong KTHinshaw RRRaub TJPadbury GEToth LN Synthesis and pharmacological evaluation of sulfone substituted HIV protease inhibitors Bioorg Med Chem Lett 7:399-402 (1997)    Article
More Info.:Get all data from this article,  Assay Method
 
Human immunodeficiency virus type 1 protease
Name:Human immunodeficiency virus type 1 protease
Synonyms:Pol polyprotein
Type:Enzyme Subunit
Mol. Mass.:10781.16
Organism:Human immunodeficiency virus type 1
Description:n/a
Residue:99
Sequence:
PQVTLWQRPLVTIKIGGQLKEALLDTGADDTVLEEMSLPGRWKPKMIGGIGGFIKVRQYD
QILIEICGHKAIGTVLVGPTPVNIIGRNLLTQIGCTLNF
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BDBM50291055
n/a
NameBDBM50291055
Synonyms:CHEMBL16636 | Pyridine-2-sulfonic acid {3-[cyclopropyl-(4-hydroxy-2-oxo-5,6,7,8,9,10-hexahydro-2H-cycloocta[b]pyran-3-yl)-methyl]-phenyl}-amide
TypeSmall organic molecule
Emp. Form.C26H28N2O5S
Mol. Mass.480.576
SMILESOc1c2CCCCCCc2oc(=O)c1C(C1CC1)c1cccc(NS(=O)(=O)c2ccccn2)c1
Structure
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