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Synthesis and biological evaluation of novel small non-peptidic HIV-1 PIs: the benzothiophene ring as an effective moiety
- Source :
- Bioorganicmedicinal chemistry letters. 22(8)
- Publication Year :
- 2012
-
Abstract
- Synthesis and biological evaluation of a new series of potential HIV-1 protease inhibitors incorporating different heterocycles are described. The variation of heteroatom in such molecules has displayed totally different biological activities and a benzothiophene containing inhibitor has shown high potency against wild type HIV-1 protease with IC50 = 60 nM, thanks to the lower desolvation penalty to be payed by such hydrophobic moiety.
- Subjects :
- Inhibitor
Stereochemistry
medicine.medical_treatment
Clinical Biochemistry
Heteroatom
Pharmaceutical Science
Heterocycles
Thiophenes
Ring (chemistry)
Biochemistry
Antiviral Agents
HIV protease
stereoselective synthesis
chemistry.chemical_compound
Synthesis
Inhibitory Concentration 50
Heterocyclic Compounds
Drug Discovery
medicine
Molecule
Moiety
Humans
Molecular Biology
Biological evaluation
Protease
Molecular Structure
Organic Chemistry
Wild type
Benzothiophene
HIV Protease Inhibitors
chemistry
HIV-1
Molecular Medicine
Subjects
Details
- ISSN :
- 14643405
- Volume :
- 22
- Issue :
- 8
- Database :
- OpenAIRE
- Journal :
- Bioorganicmedicinal chemistry letters
- Accession number :
- edsair.doi.dedup.....ff7261b9c991309eedd05b251a5888e8