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For: Malarz K, Zych D, Gawecki R, Kuczak M, Musioł R, Mrozek-Wilczkiewicz A. New derivatives of 4'-phenyl-2,2':6',2″-terpyridine as promising anticancer agents. Eur J Med Chem 2021;212:113032. [PMID: 33261897 DOI: 10.1016/j.ejmech.2020.113032] [Cited by in Crossref: 3] [Cited by in F6Publishing: 11] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Zimosz S, Zych D, Szafraniec-gorol G, Kotowicz S, Malarz K, Musioł R, Slodek A. Does the change in the length of the alkyl chain bring us closer to the compounds with the expected photophysical and biological properties? – Studies based on D-π-D-A imidazole-phenothiazine system. Journal of Molecular Liquids 2022;365:120076. [DOI: 10.1016/j.molliq.2022.120076] [Reference Citation Analysis]
2 Maroń AM, Palion-gazda J, Szłapa-kula A, Schab-balcerzak E, Siwy M, Sulowska K, Maćkowski S, Machura B. Controlling of Photophysical Behavior of Rhenium(I) Complexes with 2,6-Di(thiazol-2-yl)pyridine-Based Ligands by Pendant π-Conjugated Aryl Groups. IJMS 2022;23:11019. [DOI: 10.3390/ijms231911019] [Reference Citation Analysis]
3 Qiu L, Liu Y, Miao Y, Zhang W, Gong A, Liu Z, Asyraf MRM. Synthesis and Properties of a New Type of Terpyridine Cholesterol Derivative Gelator with Applications to Medical Treatments. International Journal of Polymer Science 2022;2022:1-16. [DOI: 10.1155/2022/3695462] [Reference Citation Analysis]
4 Liang Y, Huang W, Situ Q, Su W, Qiu W, Li S, He L, Chen J. Novel Terpyridine Conjugated Nitrogen Mustard Derivatives: Synthesis, Spectral Properties, and Anticancer Activity. Russ J Gen Chem 2022;92:725-31. [DOI: 10.1134/s1070363222040144] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Panicker RR, Sivaramakrishna A. Remarkably flexible 2,2′:6′,2″-terpyridines and their group 8–10 transition metal complexes – Chemistry and applications. Coordination Chemistry Reviews 2022;459:214426. [DOI: 10.1016/j.ccr.2022.214426] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
6 Musiol R, Malecki P, Pacholczyk M, Mularski J. Terpyridines as promising antitumor agents: an overview of their discovery and development. Expert Opin Drug Discov 2021;:1-13. [PMID: 34928186 DOI: 10.1080/17460441.2022.2017877] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
7 Liu W, Jin W, Zhu S, Chen Y, Liu B. Targeting regulated cell death (RCD) with small-molecule compounds in cancer therapy: A revisited review of apoptosis, autophagy-dependent cell death and necroptosis. Drug Discov Today 2021:S1359-6446(21)00450-5. [PMID: 34718209 DOI: 10.1016/j.drudis.2021.10.011] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
8 Adrian RA, Duarte JJ, Arman HD. Di-μ-chlorido-bis[(2,2′:6′,2′′-terpyridine-κ 3N , N ′, N ′′)copper(II)] bis(trifluoromethanesulfonate). IUCrData 2021;6. [DOI: 10.1107/s2414314621010968] [Reference Citation Analysis]
9 Wang J, Zhang PL, Ansari MF, Li S, Zhou CH. Molecular design and preparation of 2-aminothiazole sulfanilamide oximes as membrane active antibacterial agents for drug resistant Acinetobacter baumannii. Bioorg Chem 2021;113:105039. [PMID: 34091291 DOI: 10.1016/j.bioorg.2021.105039] [Cited by in Crossref: 1] [Cited by in F6Publishing: 16] [Article Influence: 1.0] [Reference Citation Analysis]
10 Malarz K, Mularski J, Kuczak M, Mrozek-Wilczkiewicz A, Musiol R. Novel Benzenesulfonate Scaffolds with a High Anticancer Activity and G2/M Cell Cycle Arrest. Cancers (Basel) 2021;13:1790. [PMID: 33918637 DOI: 10.3390/cancers13081790] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
11 Khan E. Pyridine Derivatives as Biologically Active Precursors; Organics and Selected Coordination Complexes. ChemistrySelect 2021;6:3041-64. [DOI: 10.1002/slct.202100332] [Cited by in Crossref: 3] [Cited by in F6Publishing: 9] [Article Influence: 3.0] [Reference Citation Analysis]