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For: Aneja DK, Lohan P, Arora S, Sharma C, Aneja KR, Prakash O. Synthesis of new pyrazolyl-2, 4-thiazolidinediones as antibacterial and antifungal agents. Org Med Chem Lett 2011;1:15. [PMID: 22373217 DOI: 10.1186/2191-2858-1-15] [Cited by in Crossref: 26] [Cited by in F6Publishing: 18] [Article Influence: 2.4] [Reference Citation Analysis]
Number Citing Articles
1 Khan FA, Jadhav KS, Patil RH, Shinde DB, Arote RB, Sangshetti JN. Biphenyl tetrazole-thiazolidinediones as novel bacterial peptide deformylase inhibitors: Synthesis, biological evaluations and molecular docking study. Biomedicine & Pharmacotherapy 2016;83:1146-53. [DOI: 10.1016/j.biopha.2016.08.036] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 1.7] [Reference Citation Analysis]
2 Rao KS, Ramesh P, Trivedi R, Kantam ML. Chiral squaramide catalyzed synthesis of C4 substituted chiral pyrazol-3-ol derivatives via a facile asymmetric Michael addition of 3-methyl-2-pyrazolin-5-one to β-nitrostyrenes. Tetrahedron Letters 2016;57:1227-31. [DOI: 10.1016/j.tetlet.2016.02.008] [Cited by in Crossref: 17] [Cited by in F6Publishing: 13] [Article Influence: 2.8] [Reference Citation Analysis]
3 Thuan NT, Dung DTM, Que DN, Dung PTP, Vu TK, Hahn H, Han BW, Kim Y, Han S, Nam N. Synthesis and bioevaluation of new 5-benzylidenethiazolidine-2,4-diones bearing benzenesulfonamide moiety. Med Chem Res 2015;24:3803-12. [DOI: 10.1007/s00044-015-1422-9] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
4 Trotsko N, Golus J, Kazimierczak P, Paneth A, Przekora A, Ginalska G, Wujec M. Design, synthesis and antimycobacterial activity of thiazolidine-2,4-dione-based thiosemicarbazone derivatives. Bioorganic Chemistry 2020;97:103676. [DOI: 10.1016/j.bioorg.2020.103676] [Cited by in Crossref: 9] [Cited by in F6Publishing: 2] [Article Influence: 4.5] [Reference Citation Analysis]
5 Jahan K, Khan KR, Akhter K, Romman UKR, Halim E. A convenient approach to synthesize substituted 5-Arylidene-3-m-tolyl thiazolidine-2, 4-diones by using morpholine as a catalyst and its theoretical study. PLoS One 2021;16:e0247619. [PMID: 33661961 DOI: 10.1371/journal.pone.0247619] [Reference Citation Analysis]
6 Khan FA, Patil RH, Shinde DB, Sangshetti JN. Design and synthesis of 4'-((5-benzylidene-2,4-dioxothiazolidin-3-yl)methyl)biphenyl-2-carbonitrile analogs as bacterial peptide deformylase inhibitors. Chem Biol Drug Des 2016;88:938-44. [PMID: 27401234 DOI: 10.1111/cbdd.12817] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 1.7] [Reference Citation Analysis]
7 Ammar YA, El-Sharief MA, Ghorab MM, Mohamed YA, Ragab A, Abbas SY. New Imidazolidineiminothione, Imidazolidin-2-one and Imidazoquinoxaline 
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8 Mech D, Kurowska A, Trotsko N. The Bioactivity of Thiazolidin-4-Ones: A Short Review of the Most Recent Studies. Int J Mol Sci 2021;22:11533. [PMID: 34768964 DOI: 10.3390/ijms222111533] [Reference Citation Analysis]
9 Subhashini NJP, Kumar KP, Kumar EP, Shravani P, Singh SS, Vani T, Vijjulatha M. Design and synthesis of novel (Z)-5-((1,3-diphenyl-1H-pyrazol-4-yl)methylene)-3-((1-substituted phenyl-1H-1,2,3-triazol-4-yl)methyl)thiazolidine-2,4-diones: a potential cytotoxic scaffolds and their molecular modeling studies. Mol Divers. [DOI: 10.1007/s11030-020-10093-3] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Kolluri PK, Gurrapu N, Edigi PK, N. J. P. S, Putta S, Singh SS. Design, synthesis of ( Z )‐3‐benzyl‐5‐((1‐phenyl‐3‐(3‐((1‐ substituted phenyl‐1 H ‐1,2,3‐triazol‐4‐yl)methoxy)phenyl)‐1 H ‐pyrazol‐4‐yl)methylene)thiazolidine‐2,4‐dione analogues as potential cytotoxic agents. J Heterocyclic Chem 2019;56:3244-56. [DOI: 10.1002/jhet.3720] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
11 Hamama WS, Ibrahim ME, Zoorob HH. Synthesis, DFT Study, and Antitumor Activity of Some New Heterocyclic Compounds Incorporating Isoxazole Moiety: Synthesis Some New Isoxazole compounds. Journal of the Chinese Chemical Society 2017;64:1203-12. [DOI: 10.1002/jccs.201700064] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.6] [Reference Citation Analysis]
12 Pedada KK, Zhou X, Jogiraju H, Carroll RT, Geldenhuys WJ, Lin L, Anderson DJ. A quantitative LC-MS/MS method for determination of thiazolidinedione mitoNEET ligand NL-1 in mouse serum suitable for pharmacokinetic studies. J Chromatogr B Analyt Technol Biomed Life Sci 2014;945-946:141-6. [PMID: 24334225 DOI: 10.1016/j.jchromb.2013.11.048] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 0.8] [Reference Citation Analysis]
13 Mousavi SM, Zarei M, Hashemi SA, Babapoor A, Amani AM. A conceptual review of rhodanine: current applications of antiviral drugs, anticancer and antimicrobial activities. Artificial Cells, Nanomedicine, and Biotechnology 2019;47:1132-48. [DOI: 10.1080/21691401.2019.1573824] [Cited by in Crossref: 19] [Cited by in F6Publishing: 9] [Article Influence: 6.3] [Reference Citation Analysis]
14 Abd Alhameed R, Almarhoon Z, Bukhari SI, El-Faham A, de la Torre BG, Albericio F. Synthesis and Antimicrobial Activity of a New Series of Thiazolidine-2,4-diones Carboxamide and Amino Acid Derivatives. Molecules 2019;25:E105. [PMID: 31892119 DOI: 10.3390/molecules25010105] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.7] [Reference Citation Analysis]
15 Chopra B, Dhingra AK, Prasad DN, Bhardwaj S, Dubey S. Synthesis and In Silico Molecular Docking Studies on Substituted Piperic Acid Derivatives as Inhibitors of Bacterial DNA Gyrase. CAD 2020;16:281-94. [DOI: 10.2174/1573409915666190710092032] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
16 Trotsko N, Kosikowska U, Paneth A, Wujec M, Malm A. Synthesis and antibacterial activity of new (2,4-dioxothiazolidin-5-yl/ylidene)acetic acid derivatives with thiazolidine-2,4-dione, rhodanine and 2-thiohydantoin moieties. Saudi Pharm J 2018;26:568-77. [PMID: 29844729 DOI: 10.1016/j.jsps.2018.01.016] [Cited by in Crossref: 22] [Cited by in F6Publishing: 14] [Article Influence: 5.5] [Reference Citation Analysis]
17 Khloya P, Kumar P, Mittal A, Aggarwal NK, Sharma PK. Synthesis of some novel 4-arylidene pyrazoles as potential antimicrobial agents. Org Med Chem Lett 2013;3:9. [PMID: 23981685 DOI: 10.1186/2191-2858-3-9] [Cited by in Crossref: 23] [Cited by in F6Publishing: 16] [Article Influence: 2.6] [Reference Citation Analysis]
18 Trotsko N, Przekora A, Zalewska J, Ginalska G, Paneth A, Wujec M. Synthesis and in vitro antiproliferative and antibacterial activity of new thiazolidine-2,4-dione derivatives. J Enzyme Inhib Med Chem 2018;33:17-24. [PMID: 29098896 DOI: 10.1080/14756366.2017.1387543] [Cited by in Crossref: 16] [Cited by in F6Publishing: 13] [Article Influence: 3.2] [Reference Citation Analysis]
19 Mague JT, Akkurt M, Mohamed SK, Hassan AA, Albayati MR. Methyl 2-((2Z,5Z)-4-oxo-3-phenyl-2-{2-[(1E)-1,2,3,4-tetra-hydro-naphthalen-1-yl-idene]hydrazin-1-yl-idene}-1,3-thia-zolidin-5-yl-idene)acetate. Acta Crystallogr Sect E Struct Rep Online 2014;70:o436-7. [PMID: 24826142 DOI: 10.1107/S1600536814005285] [Cited by in Crossref: 1] [Article Influence: 0.1] [Reference Citation Analysis]
20 Oraby AK, Abdellatif KRA, Abdelgawad MA, Attia KM, Dawe LN, Georghiou PE. 2,4-Disubstituted Phenylhydrazonopyrazolone and Isoxazolone Derivatives as Antibacterial Agents: Synthesis, Preliminary Biological Evaluation and Docking Studies. ChemistrySelect 2018;3:3295-301. [DOI: 10.1002/slct.201800174] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 1.8] [Reference Citation Analysis]
21 Obydennov KL, Khamidullina LA, Galushchinskiy AN, Shatunova SA, Kosterina MF, Kalinina TA, Fan Z, Glukhareva TV, Morzherin YY. Discovery of Methyl (5 Z)-[2-(2,4,5-Trioxopyrrolidin-3-ylidene)-4-oxo-1,3-thiazolidin-5-ylidene]acetates as Antifungal Agents against Potato Diseases. J Agric Food Chem 2018;66:6239-45. [PMID: 29807429 DOI: 10.1021/acs.jafc.8b02151] [Cited by in Crossref: 15] [Cited by in F6Publishing: 6] [Article Influence: 3.8] [Reference Citation Analysis]
22 S.n.c. S, Bhurta D, Kantiwal D, George G, Monga V, Paul AT. Design, synthesis, biological evaluation and molecular modelling studies of novel diaryl substituted pyrazolyl thiazolidinediones as potent pancreatic lipase inhibitors. Bioorganic & Medicinal Chemistry Letters 2017;27:3749-54. [DOI: 10.1016/j.bmcl.2017.06.069] [Cited by in Crossref: 21] [Cited by in F6Publishing: 14] [Article Influence: 4.2] [Reference Citation Analysis]
23 Chauhan D, George G, Sridhar SNC, Bhatia R, Paul AT, Monga V. Design, synthesis, biological evaluation, and molecular modeling studies of rhodanine derivatives as pancreatic lipase inhibitors. Arch Pharm (Weinheim) 2019;352:e1900029. [PMID: 31407389 DOI: 10.1002/ardp.201900029] [Cited by in Crossref: 12] [Cited by in F6Publishing: 9] [Article Influence: 4.0] [Reference Citation Analysis]
24 Demin KA, Refeld AG, Bogdanova AA, Prazdnova EV, Popov IV, Kutsevalova OY, Ermakov AM, Bren AB, Rudoy DV, Chistyakov VA, Weeks R, Chikindas ML. Mechanisms of Candida Resistance to Antimycotics and Promising Ways to Overcome It: The Role of Probiotics. Probiotics Antimicrob Proteins 2021;13:926-48. [PMID: 33738706 DOI: 10.1007/s12602-021-09776-6] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]