Pteridine–sulfonamide conjugates as dual inhibitors of carbonic anhydrases and dihydrofolate reductase with potential antitumor activity-Reference-Cited by-同舟云学术

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Pteridine–sulfonamide conjugates as dual inhibitors of carbonic anhydrases and dihydrofolate reductase with potential antitumor activity

Published:2010-07 Issue:14 Volume:18 Page:5081-5089
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Marques Sérgio M.,Enyedy Éva A.,Supuran Claudiu T.,Krupenko Natalia I.,Krupenko Sergey A.,Amélia Santos M.

Funder

Fundação para a Ciência e Tecnologia

NIH

Publisher

Elsevier BV

Subject

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

Reference30 articles.

1. Designed Multiple Ligands. An Emerging Drug Discovery Paradigm

2. Multi-target therapeutics: when the whole is greater than the sum of the parts

3. Methotrexate γ-hydroxamate derivatives as potential dual target antitumor drugs

4. Dual Inhibitors of Matrix Metalloproteinases and Carbonic Anhydrases: Iminodiacetyl-Based Hydroxamate−Benzenesulfonamide Conjugates

5. Pemetrexed disodium, a novel antifolate with multiple targets

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