Structure-Based design, synthesis and sAR of a novel series of thiopheneamidine urokinase plasminogen activator inhibitors-Reference-Cited by-同舟云学术

Structure-Based design, synthesis and sAR of a novel series of thiopheneamidine urokinase plasminogen activator inhibitors

Published:2001-06 Issue:11 Volume:11 Page:1379-1382
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Subasinghe Nalin L.,Illig Carl,Hoffman James,Rudolph M.Jonathan,Wilson Kenneth J.,Soll Richard,Randle Troy,Green David,Lewandowski Frank,Zhang Marie,Bone Roger,Spurlino John,DesJarlais Renee,Deckman Ingrid,Molloy Christopher J.,Manthey Carl,Zhou Zhau,Sharp Celia,Maguire Diane,Crysler Carl,Grasberger Bruce

Publisher

Elsevier BV

Subject

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

Reference22 articles.

1. Chapter 12. The Urokinase-type Plasminogen Activator and Its Receptor in Cancer

2. Structural Relationship Between Human High and Low Molecular Mass Urokinase

3. Clinical Impact of the Plasminogen Activation System in Tumor Invasion and Metastasis: Prognostic Relevance and Target for Therapy

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