Benzenesulfonamides with pyrimidine moiety as inhibitors of human carbonic anhydrases I, II, VI, VII, XII, and XIII-Reference-Cited by-同舟云学术

Benzenesulfonamides with pyrimidine moiety as inhibitors of human carbonic anhydrases I, II, VI, VII, XII, and XIII

Published:2013-11 Issue:22 Volume:21 Page:6937-6947
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Čapkauskaitė Edita,Zubrienė Asta,Smirnov Alexey,Torresan Jolanta,Kišonaitė Miglė,Kazokaitė Justina,Gylytė Joana,Michailovienė Vilma,Jogaitė Vaida,Manakova Elena,Gražulis Saulius,Tumkevičius Sigitas,Matulis Daumantas

Funder

Research Council of Lithuania

FP7-REGPOT-2009-1

Promotion of Student Scientific Activities

Republic of Lithuania and European Social Fund

Human Resources Development Operational Programme’s

Publisher

Elsevier BV

Subject

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

Reference37 articles.

1. Design of [(2-pyrimidinylthio)acetyl]benzenesulfonamides as inhibitors of human carbonic anhydrases

2. Carbonic anhydrases: novel therapeutic applications for inhibitors and activators

3. Carbonic Anhydrase as a Model for Biophysical and Physical-Organic Studies of Proteins and Protein−Ligand Binding

4. HUMAN CARBONIC ANHYDRASES AND CARBONIC ANHYDRASE DEFICIENCIES

5. Multiple Binding Modes of Inhibitors to Carbonic Anhydrases: How to Design Specific Drugs Targeting 15 Different Isoforms?

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