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For: Leśnikowski ZJ. Recent developments with boron as a platform for novel drug design. Expert Opin Drug Discov 2016;11:569-78. [PMID: 27080414 DOI: 10.1080/17460441.2016.1174687] [Cited by in Crossref: 52] [Cited by in F6Publishing: 29] [Article Influence: 10.4] [Reference Citation Analysis]
Number Citing Articles
1 Kellert M, Sárosi I, Rajaratnam R, Meggers E, Lönnecke P, Hey-Hawkins E. Ruthenacarborane-Phenanthroline Derivatives as Potential Metallodrugs. Molecules 2020;25:E2322. [PMID: 32429279 DOI: 10.3390/molecules25102322] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
2 Murphy N, McCarthy E, Dwyer R, Farràs P. Boron clusters as breast cancer therapeutics. J Inorg Biochem 2021;218:111412. [PMID: 33773323 DOI: 10.1016/j.jinorgbio.2021.111412] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
3 Erkmen T, Serdar BS, Ateş H, Korkmaz M, Koçtürk S. Borax Pentahydrate and Disodium Pentaborate Decahydrate Are Candidates as Anti-leukemic Drug Components by Inducing Apoptosis and Changing Bax/Bcl-2 Ratio in HL-60 Cell Line. Biol Trace Elem Res 2021. [PMID: 34184213 DOI: 10.1007/s12011-021-02802-2] [Reference Citation Analysis]
4 Nekvinda J, Różycka D, Rykowski S, Wyszko E, Fedoruk-Wyszomirska A, Gurda D, Orlicka-Płocka M, Giel-Pietraszuk M, Kiliszek A, Rypniewski W, Bachorz R, Wojcieszak J, Grüner B, Olejniczak AB. Synthesis of naphthalimide-carborane and metallacarborane conjugates: Anticancer activity, DNA binding ability. Bioorg Chem 2020;94:103432. [PMID: 31776032 DOI: 10.1016/j.bioorg.2019.103432] [Cited by in Crossref: 13] [Cited by in F6Publishing: 7] [Article Influence: 6.5] [Reference Citation Analysis]
5 Dąbrowska A, Matuszewski M, Zwoliński K, Ignaczak A, Olejniczak AB. Insight into lipophilicity of deoxyribonucleoside‑boron cluster conjugates. European Journal of Pharmaceutical Sciences 2018;111:226-37. [DOI: 10.1016/j.ejps.2017.09.036] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
6 Bednarska-Szczepaniak K, Mieczkowski A, Kierozalska A, Pavlović Saftić D, Głąbała K, Przygodzki T, Stańczyk L, Karolczak K, Watała C, Rao H, Gao ZG, Jacobson KA, Leśnikowski ZJ. Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonists. Eur J Med Chem 2021;223:113607. [PMID: 34171656 DOI: 10.1016/j.ejmech.2021.113607] [Reference Citation Analysis]
7 Wu Z, Xia MB, Bertsetseg D, Wang YH, Bao XL, Zhu WB, Tao-Xu, Chen PR, Tang HS, Yan YJ, Chen ZL. Design, synthesis and biological evaluation of novel fluoro-substituted benzimidazole derivatives with anti-hypertension activities. Bioorg Chem 2020;101:104042. [PMID: 32650179 DOI: 10.1016/j.bioorg.2020.104042] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
8 Ali F, S Hosmane N, Zhu Y. Boron Chemistry for Medical Applications. Molecules 2020;25:E828. [PMID: 32070043 DOI: 10.3390/molecules25040828] [Cited by in Crossref: 38] [Cited by in F6Publishing: 17] [Article Influence: 38.0] [Reference Citation Analysis]
9 Vincenzi M, Bednarska K, Leśnikowski ZJ. Comparative Study of Carborane- and Phenyl-Modified Adenosine Derivatives as Ligands for the A2A and A3 Adenosine Receptors Based on a Rigid in Silico Docking and Radioligand Replacement Assay. Molecules 2018;23:E1846. [PMID: 30044380 DOI: 10.3390/molecules23081846] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
10 Rykowski S, Gurda-Woźna D, Orlicka-Płocka M, Fedoruk-Wyszomirska A, Giel-Pietraszuk M, Wyszko E, Kowalczyk A, Stączek P, Bak A, Kiliszek A, Rypniewski W, Olejniczak AB. Design, Synthesis, and Evaluation of Novel 3-Carboranyl-1,8-Naphthalimide Derivatives as Potential Anticancer Agents. Int J Mol Sci 2021;22:2772. [PMID: 33803403 DOI: 10.3390/ijms22052772] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Neochoritis CG, Shaabani S, Ahmadianmoghaddam M, Zarganes-Tzitzikas T, Gao L, Novotná M, Mitríková T, Romero AR, Irianti MI, Xu R, Olechno J, Ellson R, Helan V, Kossenjans M, Groves MR, Dömling A. Rapid approach to complex boronic acids. Sci Adv 2019;5:eaaw4607. [PMID: 31281893 DOI: 10.1126/sciadv.aaw4607] [Cited by in Crossref: 15] [Cited by in F6Publishing: 6] [Article Influence: 7.5] [Reference Citation Analysis]
12 Pan S, Barroso J, Jalife S, Heine T, Asmis KR, Merino G. Fluxional Boron Clusters: From Theory to Reality. Acc Chem Res 2019;52:2732-44. [PMID: 31487150 DOI: 10.1021/acs.accounts.9b00336] [Cited by in Crossref: 39] [Cited by in F6Publishing: 9] [Article Influence: 19.5] [Reference Citation Analysis]
13 Goszczyński TM, Fink K, Boratyński J. Icosahedral boron clusters as modifying entities for biomolecules. Expert Opin Biol Ther 2018;18:205-13. [PMID: 30063861 DOI: 10.1080/14712598.2018.1473369] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
14 Bello M, Guadarrama-García C, Velasco-Silveyra LM, Farfán-García ED, Soriano-Ursúa MA. Several effects of boron are induced by uncoupling steroid hormones from their transporters in blood. Med Hypotheses 2018;118:78-83. [PMID: 30037620 DOI: 10.1016/j.mehy.2018.06.024] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 2.7] [Reference Citation Analysis]
15 Lopalco A, Lopedota AA, Laquintana V, Denora N, Stella VJ. Boric Acid, a Lewis Acid With Unique and Unusual Properties: Formulation Implications. Journal of Pharmaceutical Sciences 2020;109:2375-86. [DOI: 10.1016/j.xphs.2020.04.015] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 8.0] [Reference Citation Analysis]
16 Fernandes GFS, Denny WA, Dos Santos JL. Boron in drug design: Recent advances in the development of new therapeutic agents. Eur J Med Chem 2019;179:791-804. [PMID: 31288128 DOI: 10.1016/j.ejmech.2019.06.092] [Cited by in Crossref: 48] [Cited by in F6Publishing: 21] [Article Influence: 24.0] [Reference Citation Analysis]
17 Couto M, Alamón C, Nievas S, Perona M, Dagrosa MA, Teixidor F, Cabral P, Viñas C, Cerecetto H. Bimodal Therapeutic Agents Against Glioblastoma, One of the Most Lethal Forms of Cancer. Chemistry 2020;26:14335-40. [PMID: 32738078 DOI: 10.1002/chem.202002963] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 5.0] [Reference Citation Analysis]
18 Mieczkowski A, Kierozalska A, Białek-pietras M, Goszczyński TM, Janczak S, Olejniczak AB, Studzińska M, Paradowska E, Leśnikowski ZJ. Comparative study of inorganic, boron-rich cluster and organic, phenyl adenosine modifications: synthesis and properties. Future Medicinal Chemistry 2019;11:1267-84. [DOI: 10.4155/fmc-2018-0517] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
19 Różycka D, Korycka-Machała M, Żaczek A, Dziadek J, Gurda D, Orlicka-Płocka M, Wyszko E, Biniek-Antosiak K, Rypniewski W, Olejniczak AB. Novel Isoniazid-Carborane Hybrids Active in Vitro Against Mycobacterium tuberculosis. Pharmaceuticals (Basel) 2020;13:E465. [PMID: 33333865 DOI: 10.3390/ph13120465] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 Yan J, Yang W, Zhang Q, Yan Y. Introducing borane clusters into polymeric frameworks: architecture, synthesis, and applications. Chem Commun 2020;56:11720-34. [DOI: 10.1039/d0cc04709k] [Cited by in Crossref: 5] [Article Influence: 5.0] [Reference Citation Analysis]
21 Nekvinda J, Kugler M, Holub J, El Anwar S, Brynda J, Pospíšilová K, Růžičková Z, Řezáčová P, Grüner B. Direct Introduction of an Alkylsulfonamido Group on C‐sites of Isomeric Dicarba‐ closo ‐dodecaboranes: The Influence of Stereochemistry on Inhibitory Activity against the Cancer‐Associated Carbonic Anhydrase IX Isoenzyme. Chem Eur J 2020;26:16541-53. [DOI: 10.1002/chem.202002809] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
22 Psurski M, Łupicka-Słowik A, Adamczyk-Woźniak A, Wietrzyk J, Sporzyński A. Discovering simple phenylboronic acid and benzoxaborole derivatives for experimental oncology - phase cycle-specific inducers of apoptosis in A2780 ovarian cancer cells. Invest New Drugs 2019;37:35-46. [PMID: 29779163 DOI: 10.1007/s10637-018-0611-z] [Cited by in Crossref: 10] [Cited by in F6Publishing: 5] [Article Influence: 3.3] [Reference Citation Analysis]
23 Xiao YC, Chen XP, Deng J, Yan YH, Zhu KR, Li G, Yu JL, Brem J, Chen F, Schofield CJ, Li GB. Design and enantioselective synthesis of 3-(α-acrylic acid) benzoxaboroles to combat carbapenemase resistance. Chem Commun (Camb) 2021;57:7709-12. [PMID: 34259249 DOI: 10.1039/d1cc03026d] [Reference Citation Analysis]
24 Butcher TW, McClain EJ, Hamilton TG, Perrone TM, Kroner KM, Donohoe GC, Akhmedov NG, Petersen JL, Popp BV. Regioselective Copper-Catalyzed Boracarboxylation of Vinyl Arenes. Org Lett 2016;18:6428-31. [PMID: 27978640 DOI: 10.1021/acs.orglett.6b03326] [Cited by in Crossref: 57] [Cited by in F6Publishing: 26] [Article Influence: 11.4] [Reference Citation Analysis]
25 Grygorenko OO, Moskvina VS, Hryshchuk OV, Tymtsunik AV. Cycloadditions of Alkenylboronic Derivatives. Synthesis 2020;52:2761-80. [DOI: 10.1055/s-0040-1707159] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
26 Kavoosi S, Dey D, Islam K. Synthesis of 5-Dihydroxyboryluridine Phosphoramidite and Its Site-Specific Incorporation into Oligonucleotides for Probing Thymine DNA Glycosylase. Org Lett 2019;21:6614-8. [PMID: 31448618 DOI: 10.1021/acs.orglett.9b02042] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
27 Mereddy GR, Chakradhar A, Rutkoski RM, Jonnalagadda SC. Benzoboroxoles: Synthesis and applications in medicinal chemistry. Journal of Organometallic Chemistry 2018;865:12-22. [DOI: 10.1016/j.jorganchem.2018.03.017] [Cited by in Crossref: 20] [Cited by in F6Publishing: 5] [Article Influence: 6.7] [Reference Citation Analysis]
28 Sopchenski L, Cogo S, Dias-ntipanyj M, Elifio-espósito S, Popat K, Soares P. Bioactive and antibacterial boron doped TiO2 coating obtained by PEO. Applied Surface Science 2018;458:49-58. [DOI: 10.1016/j.apsusc.2018.07.049] [Cited by in Crossref: 16] [Cited by in F6Publishing: 4] [Article Influence: 5.3] [Reference Citation Analysis]