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Synthesis and activity of tetrapeptidic HTLV-I protease inhibitors possessing different P3-cap moieties
- Source :
- Bioorganic & Medicinal Chemistry. 16:5795-5802
- Publication Year :
- 2008
- Publisher :
- Elsevier BV, 2008.
-
Abstract
- The causative agent behind adult T-cell leukemia and tropical spastic paraparesis/HTLV-I-associated myelopathy is the human T-cell leukemia virus type 1 (HTLV-I). Tetrapeptidic HTLV-I protease inhibitors were designed on a previously reported potent inhibitor KNI-10516, with modifications at the P3-cap moieties. All the inhibitors showed high HIV-1 protease inhibitory activity (over 98% inhibition at 50 nM) and most exhibited highly potent inhibition against HTLV-I protease (IC50 values were less than 100 nM).
- Subjects :
- Models, Molecular
viruses
medicine.medical_treatment
Clinical Biochemistry
Drug Evaluation, Preclinical
Molecular Conformation
Pharmaceutical Science
Biochemistry
Virus
Microbiology
Inhibitory Concentration 50
Structure-Activity Relationship
HIV Protease
hemic and lymphatic diseases
Drug Discovery
Tropical spastic paraparesis
medicine
Aspartic Acid Endopeptidases
Humans
Protease Inhibitors
Protease inhibitor (pharmacology)
Molecular Biology
chemistry.chemical_classification
Binding Sites
Protease
Dose-Response Relationship, Drug
biology
Chemistry
Organic Chemistry
virus diseases
Stereoisomerism
medicine.disease
In vitro
Leukemia
Enzyme
Enzyme inhibitor
biology.protein
Molecular Medicine
Oligopeptides
Subjects
Details
- ISSN :
- 09680896
- Volume :
- 16
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....8a0f1ac54055a8d4bc4f2d171389cd9a
- Full Text :
- https://doi.org/10.1016/j.bmc.2008.03.055