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β-N-Biaryl ether sulfonamide hydroxamates as potent gelatinase inhibitors: Part 1. Design, synthesis, and lead identification
- Source :
- Bioorganic & Medicinal Chemistry Letters. 18:1135-1139
- Publication Year :
- 2008
- Publisher :
- Elsevier BV, 2008.
-
Abstract
- A new series of β-N-biaryl ether sulfonamide hydroxamates as novel gelatinase inhibitors is described. These compounds exhibit good potency for MMP-2 and MMP-9 without inhibiting MMP-1. The structure–activity relationships (SAR) reveal the biaryl ether type P1′ moiety together with methanesulfonamide is the optimal combination that provides inhibitory activity of MMP-9 in the single-digit nanomolar range.
- Subjects :
- Stereochemistry
Clinical Biochemistry
Gelatinase A
Pharmaceutical Science
Ether
Matrix Metalloproteinase Inhibitors
Hydroxamic Acids
Biochemistry
Chemical synthesis
Structure-Activity Relationship
chemistry.chemical_compound
Drug Discovery
Animals
Humans
Moiety
Gelatinase
Molecular Biology
chemistry.chemical_classification
Sulfonamides
Hydroxamic acid
Molecular Structure
biology
Organic Chemistry
Rats
Sulfonamide
chemistry
Gelatinases
Enzyme inhibitor
Drug Design
Pyrazines
Microsomes, Liver
biology.protein
Molecular Medicine
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 18
- Database :
- OpenAIRE
- Journal :
- Bioorganic & Medicinal Chemistry Letters
- Accession number :
- edsair.doi.dedup.....27a1009364fff483588e2f49730114c5