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For: Nocentini A, Moi D, Deplano A, Osman SM, Alothman ZA, Balboni G, Supuran CT, Onnis V. Sulfonamide/sulfamate switch with a series of piperazinylureido derivatives: Synthesis, kinetic and in silico evaluation as carbonic anhydrase isoforms I, II, IV, and IX inhibitors. European Journal of Medicinal Chemistry 2020;186:111896. [DOI: 10.1016/j.ejmech.2019.111896] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
Number Citing Articles
1 Moi D, Deplano A, Angeli A, Balboni G, Supuran CT, Onnis V. Synthesis of Sulfonamides Incorporating Piperidinyl-Hydrazidoureido and Piperidinyl-Hydrazidothioureido Moieties and Their Carbonic Anhydrase I, II, IX and XII Inhibitory Activity. Molecules 2022;27:5370. [DOI: 10.3390/molecules27175370] [Reference Citation Analysis]
2 Ghiasi M, Goli NE, Gholami S, Supuran CT. QM and QM/MM study on inhibition mechanism of polyphenolic compounds as non-classical inhibitors of α-human carbonic anhydrase (II). Theor Chem Acc 2021;140. [DOI: 10.1007/s00214-021-02839-5] [Reference Citation Analysis]
3 Aimene Y, Eychenne R, Rodriguez F, Mallet-ladeira S, Saffon-merceron N, Winum J, Nocentini A, Supuran CT, Benoist E, Seridi A. Synthesis, Crystal Structure, Inhibitory Activity and Molecular Docking of Coumarins/Sulfonamides Containing Triazolyl Pyridine Moiety as Potent Selective Carbonic Anhydrase IX and XII Inhibitors. Crystals 2021;11:1076. [DOI: 10.3390/cryst11091076] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Huo XS, Jian XE, Ou-Yang J, Chen L, Yang F, Lv DX, You WW, Rao JJ, Zhao PL. Discovery of highly potent tubulin polymerization inhibitors: Design, synthesis, and structure-activity relationships of novel 2,7-diaryl-[1,2,4]triazolo[1,5-a]pyrimidines. Eur J Med Chem 2021;220:113449. [PMID: 33895499 DOI: 10.1016/j.ejmech.2021.113449] [Cited by in Crossref: 2] [Cited by in F6Publishing: 16] [Article Influence: 2.0] [Reference Citation Analysis]
5 Kast RE. Adding high-dose celecoxib to increase effectiveness of standard glioblastoma chemoirradiation. Ann Pharm Fr 2021;79:481-8. [PMID: 33689795 DOI: 10.1016/j.pharma.2021.03.001] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
6 Mondal S. Sulfonamide synthesis under green conditions. Synthetic Communications 2021;51:1023-44. [DOI: 10.1080/00397911.2020.1870238] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
7 Ghorab MM, Soliman AM, Bua S, Supuran CT. Biological evaluation, radiosensitizing activity and structural insights of novel halogenated quinazoline-sulfonamide conjugates as selective human carbonic anhydrases IX/XII inhibitors. Bioorg Chem 2021;107:104618. [PMID: 33485104 DOI: 10.1016/j.bioorg.2020.104618] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
8 Sahasrabuddhe A, Oakley D, Chen K, McCarter JD. Development of a High-Throughput Affinity Mass Spectrometry (AMS) Platform Using Laser Diode Thermal Desorption Ionization Coupled to Mass Spectrometry (LDTD-MS). SLAS Discov 2021;26:230-41. [PMID: 33334237 DOI: 10.1177/2472555220979596] [Reference Citation Analysis]
9 Yan X, Wen J, Zhou L, Fan L, Wang X, Xu Z. Current Scenario of 1,3-oxazole Derivatives for Anticancer Activity. CTMC 2020;20:1916-37. [DOI: 10.2174/1568026620666200624161151] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
10 Ghiasi M, Gholami S. Quantum mechanical study of human carbonic anhydrase II in complex with polyamines as novel inhibitors: Kinetic and thermodynamic investigation. Computational and Theoretical Chemistry 2020;1186:112911. [DOI: 10.1016/j.comptc.2020.112911] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
11 Moi D, Nocentini A, Deplano A, Osman SM, AlOthman ZA, Piras V, Balboni G, Supuran CT, Onnis V. Appliance of the piperidinyl-hydrazidoureido linker to benzenesulfonamide compounds: Synthesis, in vitro and in silico evaluation of potent carbonic anhydrase II, IX and XII inhibitors. Bioorg Chem 2020;98:103728. [PMID: 32182519 DOI: 10.1016/j.bioorg.2020.103728] [Cited by in Crossref: 7] [Cited by in F6Publishing: 10] [Article Influence: 3.5] [Reference Citation Analysis]