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For: Ruberte AC, Sanmartin C, Aydillo C, Sharma AK, Plano D. Development and Therapeutic Potential of Selenazo Compounds. J Med Chem 2020;63:1473-89. [PMID: 31638805 DOI: 10.1021/acs.jmedchem.9b01152] [Cited by in Crossref: 26] [Cited by in F6Publishing: 21] [Article Influence: 8.7] [Reference Citation Analysis]
Number Citing Articles
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2 Ramos-Inza S, Ruberte AC, Sanmartín C, Sharma AK, Plano D. NSAIDs: Old Acquaintance in the Pipeline for Cancer Treatment and Prevention─Structural Modulation, Mechanisms of Action, and Bright Future. J Med Chem 2021;64:16380-421. [PMID: 34784195 DOI: 10.1021/acs.jmedchem.1c01460] [Reference Citation Analysis]
3 Hou W, Xu H. Incorporating Selenium into Heterocycles and Natural Products─From Chemical Properties to Pharmacological Activities. J Med Chem 2022. [PMID: 35244394 DOI: 10.1021/acs.jmedchem.1c01859] [Reference Citation Analysis]
4 Huang Y, Peng Z, Wei M, Gan C, Zhang Y, Chen S, Xiao J, Cui J. Synthesis and Antiproliferative Evaluation of Some Novel Estradiol Selenocyanates. Steroids 2022;:108992. [PMID: 35202703 DOI: 10.1016/j.steroids.2022.108992] [Reference Citation Analysis]
5 Sharifiaghdam M, Shaabani E, Sharifiaghdam Z, De Keersmaecker H, De Rycke R, De Smedt S, Faridi-Majidi R, Braeckmans K, Fraire JC. Enhanced siRNA Delivery and Selective Apoptosis Induction in H1299 Cancer Cells by Layer-by-Layer-Assembled Se Nanocomplexes: Toward More Efficient Cancer Therapy. Front Mol Biosci 2021;8:639184. [PMID: 33959633 DOI: 10.3389/fmolb.2021.639184] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Wang X, Zhong Y, Mo Z, Wu S, Xu Y, Tang H, Pan Y. Synthesis of Seleno Oxindoles via Electrochemical Cyclization of N ‐arylacrylamides with Diorganyl Diselenides. Adv Synth Catal 2021;363:208-14. [DOI: 10.1002/adsc.202001192] [Cited by in Crossref: 19] [Cited by in F6Publishing: 4] [Article Influence: 9.5] [Reference Citation Analysis]
7 Sánchez-Fernández EM, García-Hernández R, Gamarro F, Arroba AI, Aguilar-Diosdado M, Padrón JM, García Fernández JM, Ortiz Mellet C. Synthesis of sp2-Iminosugar Selenoglycolipids as Multitarget Drug Candidates with Antiproliferative, Leishmanicidal and Anti-Inflammatory Properties. Molecules 2021;26:7501. [PMID: 34946583 DOI: 10.3390/molecules26247501] [Reference Citation Analysis]
8 Makhal PN, Nandi A, Kaki VR. Insights into the Recent Synthetic Advances of Organoselenium Compounds. ChemistrySelect 2021;6:663-79. [DOI: 10.1002/slct.202004029] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 6.0] [Reference Citation Analysis]
9 Kumar M, Chhillar B, Yadav M, Sagar P, Singhal NK, Gates PJ, Butcher RJ, Singh VP. Catalytic and highly regenerable aminic organoselenium antioxidants with cytoprotective effects. Org Biomol Chem 2021;19:2015-22. [DOI: 10.1039/d0ob02368j] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 Wang R, Xie H, Lai X, Liu J, Li J, Qiu G. Visible light-enabled iron-catalyzed selenocyclization of N-methoxy-2-alkynylbenzamide. Molecular Catalysis 2021;515:111881. [DOI: 10.1016/j.mcat.2021.111881] [Cited by in Crossref: 13] [Cited by in F6Publishing: 9] [Article Influence: 13.0] [Reference Citation Analysis]
11 Hou W, Dong H, Zhang X, Wang Y, Su L, Xu H. Selenium as an emerging versatile player in heterocycles and natural products modification. Drug Discov Today 2022:S1359-6446(22)00130-1. [PMID: 35390546 DOI: 10.1016/j.drudis.2022.03.020] [Reference Citation Analysis]
12 Jastrzebska I, Grzes PA, Niemirowicz-Laskowska K, Car H. Selenosteroids - promising hybrid compounds with pleiotropic biological activity: synthesis and biological aspects. J Steroid Biochem Mol Biol 2021;213:105975. [PMID: 34418527 DOI: 10.1016/j.jsbmb.2021.105975] [Reference Citation Analysis]
13 Costa GP, Bach MF, Moraes MC, Barcellos T, Lenardão EJ, Silva MS, Alves D. Sequential Organocatalytic Synthesis of [1,2,3]Triazolo[1,5‐ a ]quinolines. Adv Synth Catal 2020;362:5044-55. [DOI: 10.1002/adsc.202000887] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
14 Xu H, Wang Y, Dong H, Zhang Y, Gu Y, Zhang S, Meng Y, Li J, Shi XJ, Ji Q, Liu L, Ma P, Ma F, Yang G, Hou W. Selenylation Chemistry Suitable for On‐Plate Parallel and On‐DNA Library Synthesis Enabling High‐Throughput Medicinal Chemistry. Angewandte Chemie. [DOI: 10.1002/ange.202206516] [Reference Citation Analysis]
15 Cheng X, Hasimujiang B, Xu Z, Cai H, Chen G, Mo G, Ruan Z. Direct Electrochemical Selenylation/Cyclization of Alkenes: Access to Functionalized Benzheterocycles. J Org Chem 2021. [PMID: 34328728 DOI: 10.1021/acs.joc.1c01267] [Reference Citation Analysis]
16 Ruberte AC, Ramos-Inza S, Aydillo C, Talavera I, Encío I, Plano D, Sanmartín C. Novel N,N'-Disubstituted Acylselenoureas as Potential Antioxidant and Cytotoxic Agents. Antioxidants (Basel) 2020;9:E55. [PMID: 31936213 DOI: 10.3390/antiox9010055] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
17 Potapov VA, Andreev MV, Musalov MV, Sterkhova IV, Amosova SV, Larina LI. Regio- and Stereoselective Synthesis of (Z,Z)-Bis(3-amino-3-oxo-1-propenyl) Selenides and Diselenides Based on 2-propynamides: A Novel Family of Diselenides with High Glutathione Peroxidase-like Activity. Inorganics 2022;10:74. [DOI: 10.3390/inorganics10060074] [Reference Citation Analysis]
18 Musalov MV, Potapov VA, Amosova SV. Efficient Synthesis of a New Family of 2,6-Disulfanyl-9-selenabicyclo[3.3.1]nonanes. Molecules 2021;26:2849. [PMID: 34064813 DOI: 10.3390/molecules26102849] [Reference Citation Analysis]
19 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]
20 Tang H, Liang Y, Cheng J, Ding K, Wang Y. Bifunctional chiral selenium-containing 1,4-diarylazetidin-2-ones with potent antitumor activities by disrupting tubulin polymerization and inducing reactive oxygen species production. Eur J Med Chem 2021;221:113531. [PMID: 34044345 DOI: 10.1016/j.ejmech.2021.113531] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Ghosh T, Wang S, Kashyap D, Jadhav RG, Rit T, Jha HC, Cousins BG, Das AK. Self-assembled benzoselenadiazole-capped tripeptide hydrogels with inherent in vitro anti-cancer and anti-inflammatory activity. Chem Commun (Camb) 2022. [PMID: 35703336 DOI: 10.1039/d2cc01160c] [Reference Citation Analysis]
22 Lin B, Lu W, Chen ZY, Zhang Y, Duan YZ, Lu X, Yan M, Zhang XJ. Enhancing the Potential of Miniature-Scale DNA-Compatible Radical Reactions via an Electron Donor-Acceptor Complex and a Reversible Adsorption to Solid Support Strategy. Org Lett 2021;23:7381-5. [PMID: 34546064 DOI: 10.1021/acs.orglett.1c02562] [Reference Citation Analysis]
23 Ostróżka-Cieślik A, Dolińska B, Ryszka F. Therapeutic Potential of Selenium as a Component of Preservation Solutions for Kidney Transplantation. Molecules 2020;25:E3592. [PMID: 32784639 DOI: 10.3390/molecules25163592] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
24 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]
25 Olomola TO, Mphahlele MJ, Gildenhuys S. Benzofuran-selenadiazole hybrids as novel α-glucosidase and cyclooxygenase-2 inhibitors with antioxidant and cytotoxic properties. Bioorg Chem 2020;100:103945. [PMID: 32450390 DOI: 10.1016/j.bioorg.2020.103945] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
26 Hellwig PS, Peglow TJ, Penteado F, Bagnoli L, Perin G, Lenardão EJ. Recent Advances in the Synthesis of Selenophenes and Their Derivatives. Molecules 2020;25:E5907. [PMID: 33322179 DOI: 10.3390/molecules25245907] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
27 Qu L, Ji L, Wang C, Luo H, Li S, Peng W, Yin F, Lu D, Liu X, Kong L, Wang X. Synthesis and evaluation of multi-target-directed ligands with BACE-1 inhibitory and Nrf2 agonist activities as potential agents against Alzheimer's disease. Eur J Med Chem 2021;219:113441. [PMID: 33862517 DOI: 10.1016/j.ejmech.2021.113441] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 V Andreev M, Potapov VA, Musalov MV, Amosova SV. (Z,Z)-Selanediylbis(2-propenamides): Novel Class of Organoselenium Compounds with High Glutathione Peroxidase-Like Activity. Regio- and Stereoselective Reaction of Sodium Selenide with 3-Trimethylsilyl-2-propynamides. Molecules 2020;25:E5940. [PMID: 33333920 DOI: 10.3390/molecules25245940] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
29 Rafique J, Rampon DS, Azeredo JB, Coelho FL, Schneider PH, Braga AL. Light-mediated Seleno-Functionalization of Organic Molecules: Recent Advances. Chem Rec 2021. [PMID: 33656248 DOI: 10.1002/tcr.202100006] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
30 Kumar M, Yadav M, Chhillar B, Singh VP. Regenerable Radical‐Trapping and Preventive Selenazolonamine Antioxidants. Asian J Org Chem 2021;10:1492-9. [DOI: 10.1002/ajoc.202100169] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
31 Qiao Z, Wei N, Jin L, Zhang H, Luo J, Zhang Y, Wang K. The Mpro structure-based modifications of ebselen derivatives for improved antiviral activity against SARS-CoV-2 virus. Bioorg Chem 2021;117:105455. [PMID: 34740055 DOI: 10.1016/j.bioorg.2021.105455] [Reference Citation Analysis]
32 Musalov MV, Potapov VA, Yakimov VA, Musalova MV, Maylyan AA, Zinchenko SV, Amosova SV. A Regioselective Synthesis of Novel Functionalized Organochalcogen Compounds by Chalcogenocyclofunctionalization Reactions Based on Chalcogen Halides and Natural Products. Molecules 2021;26:3729. [PMID: 34207301 DOI: 10.3390/molecules26123729] [Reference Citation Analysis]
33 Gan H, Cao M, Wu H. Synthesis of 2‐Arylbenzoselenazoles from Se‐mediated Redox Condensation of 2‐Chloronitrobenzene and Arylmethyl Chloride. ChemistrySelect 2020;5:4548-51. [DOI: 10.1002/slct.202000642] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]