Biological activity of oxadiazole and thiadiazole derivatives-Reference-Cited by-同舟云学术

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Biological activity of oxadiazole and thiadiazole derivatives

Published:2022-05 Issue:9-10 Volume:106 Page:3489-3505
ISSN:0175-7598
Container-title:Applied Microbiology and Biotechnology
language:en
Short-container-title:Appl Microbiol Biotechnol

Author:

Atmaram Upare Abhay,Roopan Selvaraj Mohana^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Applied Microbiology and Biotechnology,General Medicine,Biotechnology

Link

https://link.springer.com/content/pdf/10.1007/s00253-022-11969-0.pdf

Reference82 articles.

1. Aguiar DF, Dutra LAA, Dantas WM, Carvalho GC, Lemes RP, Pessoa CO, Paier CK, Araujo PL, Araujo ES, Pena LJ, de Oliveira RN (2019) Synthesis, antitumor and cytotoxic activity of new adamantyl o-acylamidoximes and 3-aryl-5-adamantane1,2,4-oxadiazole derivatives. Chem Select 4:9112–9118. https://doi.org/10.1002/slct.201901285

2. Almansour AL, Kumar RS, Arumugam N, Sriram DA (2012) Solvent free, four-component synthesis and 1,3-dipolar cycloaddition of 4(H)-pyrans with nitrile oxides: synthesis and discovery of antimycobacterial activity of enantiomerically pure 1,2,4-oxadiazoles. Eur J Med Chem 53:416–423. https://doi.org/10.1016/j.ejmech.2012.04.021

3. Al-Omar MA, Amar AEE, Wahab AA (2011) Synthesis and antimicrobial activity of some heterocyclic 2, 6-bis(substituted)-1,3,4-thiadiazolo-, oxadiazolo-, and oxathiazolidino-pyridine derivatives from 2,6-pyridine dicarboxylic acid dihydrazide. J Heterocycl Chem 48(5):1103–1110. https://doi.org/10.1002/jhet.690

4. Altıntop MD, Ciftci HI, Radwan MO, Sever B, Kaplancıkl ZA, Ali Taha FS, Koga R, Fujita M, Otsuka M, Özdemir A (2018) Design, synthesis, and biological evaluation of novel 1,3,4-thiadiazole derivatives as potential antitumor agents against chronic myelogenous leukemia, striking effect of nitrothiazole moiety. Molecules 23(1):59–76. https://doi.org/10.3390/molecules23010059

5. Amin KM, Taha AM, George RF, Mohamed NM, Elsenduny FF (2017) Synthesis, antitumor activity evaluation, and DNA-binding study of coumarin-based agents. Arch Pharm Chem Life Sci 351(1):1–18. https://doi.org/10.1002/ardp.201700199

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1. 2,5-Disubstituted structures of 1,3,4-oxadiazole and 1,3,4-thiodiazole for anti-inflammatory potential: DFT approach for the structural aspects;Journal of Molecular Structure;2024-12

2. Synthesis, characterization, antimicrobial screening and in-silico studies of thiadiazole derivatives;Journal of Molecular Structure;2024-11

3. Synthesis, spectroscopic, electrochemistry and antioxidant properties of benzofuroxan and 2H-benzimidazole 1,3-dioxide derivatives: Effects of conjugation with electron-acceptor 1,2,3-triazolyl-1,2,4-oxadiazole;Journal of Molecular Structure;2024-09

4. Synthesis of Hybrid Molecules with Imidazole-1,3,4-thiadiazole Core and Evaluation of Biological Activity on Trypanosoma cruzi and Leishmania donovani;Molecules;2024-08-30

5. Unveiling the Anti-cancer Potential of Oxadiazole Derivatives: A Comprehensive Exploration of Structure-Activity Relationships and Chemico-Biological Insights;Medicinal Chemistry;2024-08-29

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