Synthesis, tuberculosis inhibitory activity, and SAR study of N-substituted-phenyl-1,2,3-triazole derivatives-Reference-Cited by-同舟云学术

Synthesis, tuberculosis inhibitory activity, and SAR study of N-substituted-phenyl-1,2,3-triazole derivatives

Published:2006-12 Issue:24 Volume:14 Page:8644-8653
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Costa Marilia S.,Boechat Núbia,Rangel Érica A.,da Silva Fernando de C.,de Souza Alessandra M.T.,Rodrigues Carlos R.,Castro Helena C.,Junior Ivan N.,Lourenço Maria Cristina S.,Wardell Solange M.S.V.,Ferreira Vitor F.

Publisher

Elsevier BV

Subject

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

Reference51 articles.

1. Synthesis of galactopyranosyl amino alcohols as a new class of antitubercular and antifungal agents

2. World Health Organization - WHO/HTM/TB/2006— http://www.who.int/tb.

3. Fighting tuberculosis: An old disease with new challenges

4. Azole-antifungal binding to a novel cytochrome P450 from Mycobacterium tuberculosis : implications for treatment of tuberculosis 2 2Abbreviations: CYP, cytochrome P450; CYP51, lanosterol-14α-demethylase; MT, Mycobacterium tuberculosis and PCR, polymerase chain reaction.

5. Genotypic patterns of multiple isolates of M. tuberculosis from tuberculous HIV patients

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