Isoniazid–phytochemical conjugation: A new approach for potent and less toxic anti‐TB drug development-Reference-Cited by-同舟云学术

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Isoniazid–phytochemical conjugation: A new approach for potent and less toxic anti‐TB drug development

Published:2020-05-14 Issue:2 Volume:96 Page:714-730
ISSN:1747-0277
Container-title:Chemical Biology & Drug Design
language:en
Short-container-title:Chem Biol Drug Des

Author:

Swain Shasank S.¹²^ORCID,Paidesetty Sudhir K.³^ORCID,Padhy Rabindra N.²^ORCID,Hussain Tahziba¹^ORCID

Affiliation:

1. Division of Microbiology and NCDs ICMR‐Regional Medical Research Centre Bhubaneswar India

2. Central Research Laboratory Institute of Medical Sciences and SUM Hospital Siksha ‘O’ Anusandhan Deemed to be University Bhubaneswar India

3. Department of Pharmaceutical Chemistry School of Pharmaceutical Sciences Siksha ‘O’ Anusandhan Deemed to be University Bhubaneswar India

Funder

ICMR-Young Scientist Scheme

Publisher

Wiley

Subject

Molecular Medicine,Biochemistry,Drug Discovery,Pharmacology,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cbdd.13685

Reference138 articles.

1. Synthesis, antitubercular activity and pharmacokinetic studies of some schiff bases derived from 1- alkylisatin and isonicotinic acid hydrazide (inh)

2. Addressing the Challenges of Tuberculosis: A Brief Historical Account

3. Betulinic Acid: Recent Advances in Chemical Modifications, Effective Delivery, and Molecular Mechanisms of a Promising Anticancer Therapy

4. Downregulation of katG expression is associated with isoniazid resistance in Mycobacterium tuberculosis

5. Hybrid compounds of ent-beyerane diterpenoid isosteviol with pyridinecarboxylic acid hydrazides. Synthesis, structure, and antitubercular activity

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4. Experimental, spectroscopic, and theoretical investigation on structural and anticancer activities of Schiff bases derived from isonicotinohydrazide;Journal of Molecular Structure;2023-12

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