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Cited by in F6Publishing
For: Sharma A, Agrahari AK, Rajkhowa S, Tiwari VK. Emerging impact of triazoles as anti-tubercular agent. Eur J Med Chem 2022;238:114454. [PMID: 35597009 DOI: 10.1016/j.ejmech.2022.114454] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Dhameja M, Kumar H, Kurella S, Singh R, Uma A, Gupta P. Inhibition of α-glucosidase enzyme by 'click'-inspired pharmacophore framework 1,3,4-thiadiazole-1,2,3-triazole hybrids. Future Med Chem 2023. [PMID: 36942781 DOI: 10.4155/fmc-2022-0289] [Reference Citation Analysis]
2 Thanh ND, Hai DS, Huyen LT, Hanh NT, Anh HH, Bich VTN, Hien PTT, Toan VN, Van HTK, Giang NTK. 1H-1,2,3-Triazole-4H-chromene-D-glucose hybrid compounds: Synthesis and inhibitory activity against Mycobacterium tuberculosis protein tyrosine phosphatase B. Arch Pharm (Weinheim) 2023;356:e2200459. [PMID: 36417559 DOI: 10.1002/ardp.202200459] [Reference Citation Analysis]
3 Jin B, Song Y, Ma Y, Zhou Y, Tang G, Wang Y. Syntheses, crystal structure, luminescent properties and Hirshfeld surface of a set of triazole-based salts. Journal of Molecular Structure 2023. [DOI: 10.1016/j.molstruc.2023.134980] [Reference Citation Analysis]
4 Maphupha MM, Vidov A, de Koning CB, Brady D. Laccase-catalysed azide-alkyne cycloadditions: Synthesis of benzothiazole and benzimidazole fused 1,2,3-triazole derivatives by copper containing oxidoreductase enzymes. Biocatalysis and Biotransformation 2022. [DOI: 10.1080/10242422.2022.2140588] [Reference Citation Analysis]
5 Dai J, Tian S, Yang X, Liu Z. Synthesis methods of 1,2,3-/1,2,4-triazoles: A review. Front Chem 2022;10:891484. [DOI: 10.3389/fchem.2022.891484] [Reference Citation Analysis]
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