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For: Swain B, Angeli A, Singh P, Supuran CT, Arifuddin M. New coumarin/sulfocoumarin linked phenylacrylamides as selective transmembrane carbonic anhydrase inhibitors: Synthesis and in-vitro biological evaluation. Bioorg Med Chem 2020;28:115586. [PMID: 32631564 DOI: 10.1016/j.bmc.2020.115586] [Cited by in Crossref: 5] [Cited by in F6Publishing: 11] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
1 Francesconi O, Corzana F, Kontogianni G, Pesciullesi G, Gualdani R, Supuran CT, Angeli A, Kavasi RM, Chatzinikolaidou M, Nativi C. Lipoyl-Based Antagonists of Transient Receptor Potential Cation A (TRPA1) Downregulate Osteosarcoma Cell Migration and Expression of Pro-Inflammatory Cytokines. ACS Pharmacol Transl Sci . [DOI: 10.1021/acsptsci.2c00114] [Reference Citation Analysis]
2 Tanini D, Capperucci A, Locuoco M, Ferraroni M, Costantino G, Angeli A, Supuran CT. Benzoselenoates: A novel class of carbonic anhydrase inhibitors. Bioorg Chem 2022;122:105751. [PMID: 35344894 DOI: 10.1016/j.bioorg.2022.105751] [Reference Citation Analysis]
3 Chen D, Nie X, Feng Q, Zhang Y, Wang Y, Wang Q, Huang L, Huang S, Liao S. Electrochemical Oxo-Fluorosulfonylation of Alkynes under Air: Facile Access to β-Keto Sulfonyl Fluorides. Angew Chem Int Ed Engl 2021;60:27271-6. [PMID: 34729882 DOI: 10.1002/anie.202112118] [Cited by in F6Publishing: 8] [Reference Citation Analysis]
4 Chen D, Nie X, Feng Q, Zhang Y, Wang Y, Wang Q, Huang L, Huang S, Liao S. Electrochemical Oxo‐Fluorosulfonylation of Alkynes under Air: Facile Access to β‐Keto Sulfonyl Fluorides. Angew Chem 2021;133:27477-82. [DOI: 10.1002/ange.202112118] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
5 Singh P, Kumar Sigalapalli D, Sridhar Goud N, Swain B, Kumar Sahoo S, Angeli A, Shaik AB, Madhavi Yaddanapudi V, Supuran CT, Arifuddin M. Ureidosulfocoumarin Derivatives As Selective and Potent Carbonic Anhydrase IX and XII Inhibitors. ChemMedChem 2021;:e202100725. [PMID: 34898017 DOI: 10.1002/cmdc.202100725] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Lv Z, Jialin Zang, Xing Y, Yang J, Bu M. Synthesis and Biological Evaluation of (Thiophene-2-yl)-4H-Chromen-7-yl-Sulfonate Derivatives. Russ J Bioorg Chem 2021;47:1097-104. [DOI: 10.1134/s1068162021050368] [Reference Citation Analysis]
7 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]
8 Sahoo SK, Rani B, Gaikwad NB, Ahmad MN, Kaul G, Shukla M, Nanduri S, Dasgupta A, Chopra S, Yaddanapudi VM. Synthesis and structure-activity relationship of new chalcone linked 5-phenyl-3-isoxazolecarboxylic acid methyl esters potentially active against drug resistant Mycobacterium tuberculosis. Eur J Med Chem 2021;222:113580. [PMID: 34116324 DOI: 10.1016/j.ejmech.2021.113580] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
9 Zaki I, El-sayed EH, Radwan EM. Synthesis and Antiproliferative Activity of Some New Coumarin Derivatives Derived from 8-Hydroxycoumarin. Russ J Bioorg Chem 2021;47:514-23. [DOI: 10.1134/s106816202102028x] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Thacker PS, Srikanth D, Angeli A, Singh P, Chinchilli KK, Arifuddin M, Supuran CT. Coumarin-Thiourea Hybrids Show Potent Carbonic Anhydrase IX and XIII Inhibitory Action. ChemMedChem 2021;16:1252-6. [PMID: 33346945 DOI: 10.1002/cmdc.202000915] [Cited by in F6Publishing: 4] [Reference Citation Analysis]
11 Carneiro A, Matos MJ, Uriarte E, Santana L. Trending Topics on Coumarin and Its Derivatives in 2020. Molecules 2021;26:501. [PMID: 33477785 DOI: 10.3390/molecules26020501] [Cited by in Crossref: 4] [Cited by in F6Publishing: 29] [Article Influence: 4.0] [Reference Citation Analysis]