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For: Krasowska D, Iraci N, Santi C, Drabowicz J, Cieslak M, Kaźmierczak-Barańska J, Palomba M, Królewska-Golińska K, Magiera J, Sancineto L. Diselenides and Benzisoselenazolones as Antiproliferative Agents and Glutathione-S-Transferase Inhibitors. Molecules 2019;24:E2914. [PMID: 31405214 DOI: 10.3390/molecules24162914] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 4.3] [Reference Citation Analysis]
Number Citing Articles
1 Singh A, Kaushik A, Dhau JS, Kumar R. Exploring coordination preferences and biological applications of pyridyl-based organochalcogen (Se, Te) ligands. Coordination Chemistry Reviews 2022;450:214254. [DOI: 10.1016/j.ccr.2021.214254] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 9.0] [Reference Citation Analysis]
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3 Ekumah J, Ma Y, Akpabli-tsigbe NDK, Kwaw E, Ma S, Hu J. Global soil distribution, dietary access routes, bioconversion mechanisms and the human health significance of selenium: A review. Food Bioscience 2021;41:100960. [DOI: 10.1016/j.fbio.2021.100960] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
4 Chuai H, Zhang SQ, Bai H, Li J, Wang Y, Sun J, Wen E, Zhang J, Xin M. Small molecule selenium-containing compounds: Recent development and therapeutic applications. Eur J Med Chem 2021;223:113621. [PMID: 34217061 DOI: 10.1016/j.ejmech.2021.113621] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Heredia AA, Soria-castro SM, Castro-godoy WD, Lemir ID, López-vidal M, Bisogno FR, Argüello JE, Oksdath-mansilla G. Multistep Synthesis of Organic Selenides under Visible Light Irradiation: A Continuous-Flow Approach. Org Process Res Dev 2020;24:540-5. [DOI: 10.1021/acs.oprd.9b00548] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
6 Mangiavacchi F, Coelho Dias IF, Di Lorenzo I, Grzes P, Palomba M, Rosati O, Bagnoli L, Marini F, Santi C, Lenardao EJ, Sancineto L. Sweet Selenium: Synthesis and Properties of Selenium-Containing Sugars and Derivatives. Pharmaceuticals (Basel) 2020;13:E211. [PMID: 32859124 DOI: 10.3390/ph13090211] [Cited by in Crossref: 9] [Cited by in F6Publishing: 5] [Article Influence: 4.5] [Reference Citation Analysis]
7 Nogueira CW, Barbosa NV, Rocha JBT. Toxicology and pharmacology of synthetic organoselenium compounds: an update. Arch Toxicol 2021;95:1179-226. [PMID: 33792762 DOI: 10.1007/s00204-021-03003-5] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 6.0] [Reference Citation Analysis]
8 Etxebeste-Mitxeltorena M, Plano D, Astrain-Redín N, Morán-Serradilla C, Aydillo C, Encío I, Moreno E, Espuelas S, Sanmartín C. New Amides and Phosphoramidates Containing Selenium: Studies on Their Cytotoxicity and Antioxidant Activities in Breast Cancer. Antioxidants (Basel) 2021;10:590. [PMID: 33920484 DOI: 10.3390/antiox10040590] [Reference Citation Analysis]
9 Nascimento V, Cordeiro PS, Arca M, Marini F, Sancineto L, Braga AL, Lippolis V, Iwaoka M, Santi C. Fast and easy conversion of ortho amidoaryldiselenides into the corresponding ebselen-like derivatives driven by theoretical investigations. New J Chem 2020;44:9444-51. [DOI: 10.1039/d0nj01605e] [Cited by in Crossref: 6] [Article Influence: 3.0] [Reference Citation Analysis]
10 Santi C, Scimmi C, Sancineto L. Ebselen and Analogues: Pharmacological Properties and Synthetic Strategies for Their Preparation. Molecules 2021;26:4230. [PMID: 34299505 DOI: 10.3390/molecules26144230] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
11 Alcolea V, Pérez-Silanes S. Selenium as an interesting option for the treatment of Chagas disease: A review. Eur J Med Chem 2020;206:112673. [PMID: 32810750 DOI: 10.1016/j.ejmech.2020.112673] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
12 Osmanov VK, Askerov RK, Chipinsky EV, Borisova GN, Khrustalev VN, Chizhov AO, Peregudov AS, Cisterna J, Borisov AV, Brito I. 4-(3-Methoxyphenyl)-5-(2-thienylmethyl)-2,4-dihydro-3H-1,2,4-triazole-3-selone: Synthesis, structural characteristics and reactions. Journal of Molecular Structure 2021;1227:129537. [DOI: 10.1016/j.molstruc.2020.129537] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]