Inhibition of matrix metalloproteinases by N-carboxyalkyl dipeptides: Enhanced potency and selectivity with substituted P1′ homophenylalanines-Reference-Cited by-同舟云学术

Inhibition of matrix metalloproteinases by N-carboxyalkyl dipeptides: Enhanced potency and selectivity with substituted P1′ homophenylalanines

Published:1995-10 Issue:20 Volume:5 Page:2441-2446
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Sahoo Soumya P.,Caldwell Charles G.,Chapman Kevin T.,Durette Philippe L.,Esser Craig K.,Kopka Ihor E.,Polo Scott A.,Sperow Kelly M.,Niedzwiecki Lisa M.,Izquierdo-Martin Maria,Chang Benedict C.,Harrison Richard K.,Stein Ross L.,MacCoss Malcolm,Hagmann William K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference23 articles.

1. The origin of matrix metalloproteinases and their familial relationships

2. Metalloproteinases and their inhibitors in matrix remodeling

3. The matrix-degrading metalloproteinases

4. Evidence for metalloproteinase and metalloproteinase inhibitor imbalance in human osteoarthritic cartilage.

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