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Cited by in F6Publishing
For: Prakash O, Aneja DK, Lohan P, Hussain K, Arora S, Sharma C, Aneja KR. Synthesis and antimicrobial activity of 5-((3-aryl-1-phenyl-1H-pyrazol-4-yl)methylene)thiazolidine-2,4-diones. Med Chem Res 2012;21:2961-8. [DOI: 10.1007/s00044-011-9829-4] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 0.8] [Reference Citation Analysis]
Number Citing Articles
1 Viveka S, Dinesha, Shama P, Nagaraja GK, Deepa N, Sreenivasa MY. Design, synthesis, and pharmacological studies of some new Mannich bases and S-alkylated analogs of pyrazole integrated 1,3,4-oxadiazole. Res Chem Intermed 2016;42:2597-617. [DOI: 10.1007/s11164-015-2170-7] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
2 Sengupta S, Goswami A, Mondal R. Silver-promoted gelation studies of an unorthodox chelating tripodal pyridine–pyrazole-based ligand: templated growth of catalytic silver nanoparticles, gas and dye adsorption. New J Chem 2014;38:2470. [DOI: 10.1039/c3nj01334k] [Cited by in Crossref: 20] [Cited by in F6Publishing: 14] [Article Influence: 2.5] [Reference Citation Analysis]
3 Sengupta S, Mondal R. Elusive Nanoscale Metal-Organic-Particle-Supported Metallogel Formation Using a Nonconventional Chelating Pyridine-Pyrazole-Based Bis-Amide Ligand. Chem Eur J 2013;19:5537-41. [DOI: 10.1002/chem.201204242] [Cited by in Crossref: 23] [Cited by in F6Publishing: 20] [Article Influence: 2.6] [Reference Citation Analysis]
4 Kumar H, Deep A, Marwaha RK. Chemical Synthesis, Mechanism of Action and Anticancer Potential of Medicinally Important Thiazolidin-2,4-dione Derivatives: A Review. MRMC 2019;19:1474-516. [DOI: 10.2174/1389557519666190513093618] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
5 Naim MJ, Alam MJ, Ahmad S, Nawaz F, Shrivastava N, Sahu M, Alam O. Therapeutic journey of 2,4-thiazolidinediones as a versatile scaffold: An insight into structure activity relationship. European Journal of Medicinal Chemistry 2017;129:218-50. [DOI: 10.1016/j.ejmech.2017.02.031] [Cited by in Crossref: 41] [Cited by in F6Publishing: 29] [Article Influence: 8.2] [Reference Citation Analysis]