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TargetGag-Pol polyprotein [489-587]
LigandBDBM50052738
Substrate/Competitorn/a
Meas. Tech.ChEMBL_159317 (CHEMBL769370)
IC50 0.3±n/a nM
Citation Kim, CUMcGee, LRKrawczyk, SHHarwood, EHarada, YSwaminathan, SBischofberger, NChen, MSCherrington, JMXiong, SFGriffin, LCundy, KCLee, AYu, BGulnik, SErickson, JW New series of potent, orally bioavailable, non-peptidic cyclic sulfones as HIV-1 protease inhibitors. J Med Chem39:3431-4 (1996) [PubMed]  Article
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
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  Blast E-value cutoff:
BDBM50052738
n/a
NameBDBM50052738
Synonyms:(2R,3R,4R,5R,6R,7R)-2,7-Dibenzyl-1,1-dioxo-3,6-bis-(thiazol-5-ylmethoxy)-1lambda*6*-thiepane-4,5-diol | CHEMBL326764
TypeSmall organic molecule
Emp. Form.C28H30N2O6S3
Mol. Mass.586.743
SMILESO[C@@H]1[C@@H](O)[C@@H](OCc2cncs2)[C@@H](Cc2ccccc2)S(=O)(=O)[C@H](Cc2ccccc2)[C@@H]1OCc1cncs1
Structure
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