Antimycobacterial compounds. Optimization of the BM 212 structure, the lead compound for a new pyrrole derivative class-Reference-Cited by-同舟云学术

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Antimycobacterial compounds. Optimization of the BM 212 structure, the lead compound for a new pyrrole derivative class

Published:2005-02 Issue:4 Volume:13 Page:1221-1230
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Biava Mariangela,Porretta Giulio Cesare,Poce Giovanna,Deidda Delia,Pompei Raffaello,Tafi Andrea,Manetti Fabrizio

Publisher

Elsevier BV

Subject

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

Reference22 articles.

1. Epidemiology of infection by nontuberculous mycobacteria

2. Recent developments in epidemiology, treatment, and diagnosis of tuberculosis

3. Active Tuberculosis in Individuals Infected with Human Immunodeficiency Virus after Isoniazid Prophylaxis

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1. Pyrrole: A Decisive Scaffold for the Development of Therapeutic Agents and Structure‐Activity Relationship;ChemMedChem;2023-11-22

2. Synthesis, biological evaluation and docking studies of silicon incorporated diarylpyrroles as MmpL3 inhibitors: An effective strategy towards development of potent anti-tubercular agents;European Journal of Medicinal Chemistry;2023-11

3. Targeting mycobacterial membranes and membrane proteins: Progress and limitations;Bioorganic & Medicinal Chemistry;2023-03

4. A Comprehensive Review on Journey of Pyrrole Scaffold Against Multiple Therapeutic Targets;Anti-Cancer Agents in Medicinal Chemistry;2022-11

5. Visible light photocatalysis in the synthesis of pharmaceutically relevant heterocyclic scaffolds;Organic Chemistry Frontiers;2022

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