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For: Kumar M, Kumar V, Gupta GK. Synthesis, antibacterial evaluation, and SAR study of some novel 3-aryl/heteroaryl-9-methyl-1,2,4-triazolo-[4,3-a]-quinoline derivatives. Med Chem Res 2015;24:1857-68. [DOI: 10.1007/s00044-014-1254-z] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.9] [Reference Citation Analysis]
Number Citing Articles
1 Kamal R, Kumar V, Kumar R. Hypervalent-Iodine(III)-Mediated Oxidative Methodology for the Synthesis of Fused Triazoles. Chem Asian J 2016;11:1988-2000. [DOI: 10.1002/asia.201600119] [Cited by in Crossref: 20] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
2 Gao F, Wang T, Xiao J, Huang G. Antibacterial activity study of 1,2,4-triazole derivatives. Eur J Med Chem 2019;173:274-81. [PMID: 31009913 DOI: 10.1016/j.ejmech.2019.04.043] [Cited by in Crossref: 71] [Cited by in F6Publishing: 46] [Article Influence: 23.7] [Reference Citation Analysis]
3 Kumar S, Sukhvinder, Kumar V, Gupta GK, Beniwal V, Abdmouleh F, Ketata E, El Arbi M. Antibacterial, tyrosinase, and DNA photocleavage studies of some triazolylnucleosides. Nucleosides Nucleotides Nucleic Acids 2017;36:543-51. [PMID: 28854118 DOI: 10.1080/15257770.2017.1342830] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 0.8] [Reference Citation Analysis]
4 Zhang J, Wang S, Ba Y, Xu Z. 1,2,4-Triazole-quinoline/quinolone hybrids as potential anti-bacterial agents. European Journal of Medicinal Chemistry 2019;174:1-8. [DOI: 10.1016/j.ejmech.2019.04.033] [Cited by in Crossref: 44] [Cited by in F6Publishing: 25] [Article Influence: 14.7] [Reference Citation Analysis]
5 Kumar V, Kumar M, Kumar S. (Diacetoxyiodo)Benzene Mediated Fused 1,2,4-Triazole Derivatives: Synthetic and Medicinal Perspective. MROC 2018;16:12-25. [DOI: 10.2174/1570193x15666180406142116] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
6 Li Q, Chen P, Yang H, Luo M, You W, Zhao P. Synthesis, antiproliferative evaluation, and structure–activity relationships of novel triazole–isoindoline hybrids bearing 3,4,5-trimethoxyphenyl moiety. Chem Pap 2018;72:651-9. [DOI: 10.1007/s11696-017-0311-8] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.8] [Reference Citation Analysis]