Literature DB >> 30255953

Novel sulfamate derivatives of menthol: Synthesis, characterization, and cholinesterases and carbonic anhydrase enzymes inhibition properties.

Shahla Daryadel1, Ufuk Atmaca1,2, Parham Taslimi1, İlhami Gülçin1, Murat Çelik1.   

Abstract

Sulfamates have a large spectrum of biological activities including enzyme inhibition. Eight sulfamates derived from menthol (2a-h) were synthesized. Also, in the other section of this study, novel sulfamate derivatives of menthol were tested against some metabolic enzymes including acetylcholinesterase (AChE), butyrylcholinesterase (BChE), and carbonic anhydrase I and II enzymes (hCAs I and II). The newly synthesized novel menthol sulfamate and menthol carbonyl sulfamate derivatives showed Ki values in the range of 34.37 ± 8.17 to 53.40 ± 10.61 nM against hCA I, 12.91 ± 4.57 to 38.67 ± 6.22 nM against hCA II, 111.17 ± 52.36 to 522.86 ± 120.08 nM against AChE, and 50.01 ± 11.73 to 109.63 ± 50.08 nM against BChE. As a result, the novel menthol sulfamate and menthol carbonyl sulfamate derivatives can be promising Alzheimer's disease drug candidates and novel hCA I and hCA II enzymes inhibitors.
© 2018 Deutsche Pharmazeutische Gesellschaft.

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Keywords:  acetylcholinesterase; butyrylcholinesterase; carbonic anhydrase; enzyme inhibition; sulfamate

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Year:  2018        PMID: 30255953     DOI: 10.1002/ardp.201800209

Source DB:  PubMed          Journal:  Arch Pharm (Weinheim)        ISSN: 0365-6233            Impact factor:   3.751


  1 in total

1.  One-pot synthesis of oxazolidinones and five-membered cyclic carbonates from epoxides and chlorosulfonyl isocyanate: theoretical evidence for an asynchronous concerted pathway.

Authors:  Esra Demir; Ozlem Sari; Yasin Çetinkaya; Ufuk Atmaca; Safiye Sağ Erdem; Murat Çelik
Journal:  Beilstein J Org Chem       Date:  2020-07-21       Impact factor: 2.883

  1 in total

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