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For: Xu Y, Zhang Z, Shi J, Liu X, Tang W. Recent developments of synthesis and biological activity of sultone scaffolds in medicinal chemistry. Arabian Journal of Chemistry 2021;14:103037. [DOI: 10.1016/j.arabjc.2021.103037] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 5.0] [Reference Citation Analysis]
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1 Dobrydnev AV, Vashchenko BV, Popova MV, Volovenko YM. A Study on Sulfonylation of Cyanohydrins with α‐Functionalized Sulfonyl Chlorides. ChemistrySelect 2022;7. [DOI: 10.1002/slct.202202401] [Reference Citation Analysis]
2 Kumari S, Maddeboina K, Bachu RD, Boddu SHS, Trippier PC, Tiwari AK. Pivotal role of nitrogen heterocycles in Alzheimer's disease drug discovery. Drug Discov Today 2022:S1359-6446(22)00292-6. [PMID: 35868626 DOI: 10.1016/j.drudis.2022.07.007] [Reference Citation Analysis]
3 Pourabdi L, Küçükkılınç TT, Khoshtale F, Ayazgök B, Nadri H, Farokhi Alashti F, Forootanfar H, Akbari T, Shafiei M, Foroumadi A, Sharifzadeh M, Shafiee Ardestani M, Abaee MS, Firoozpour L, Khoobi M, Mojtahedi MM. Synthesis of New 3-Arylcoumarins Bearing N-Benzyl Triazole Moiety: Dual Lipoxygenase and Butyrylcholinesterase Inhibitors With Anti-Amyloid Aggregation and Neuroprotective Properties Against Alzheimer’s Disease. Front Chem 2022;9:810233. [DOI: 10.3389/fchem.2021.810233] [Reference Citation Analysis]
4 Zhang H, Wu C, Chen X, Zhang Z, Jiang X, Qin HL, Tang W. Novel pyridine-containing sultones: Structure-activity relationship and biological evaluation as selective AChE inhibitors for the treatment of Alzheimer's disease. ChemMedChem 2021. [PMID: 34036731 DOI: 10.1002/cmdc.202100272] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]