New arylidene-linked chromane-2,4-dione analogs as potential leads for diabetic management; syntheses, α-amylase inhibitory, and radical scavenging activities-Reference-Cited by-同舟云学术

New arylidene-linked chromane-2,4-dione analogs as potential leads for diabetic management; syntheses, α-amylase inhibitory, and radical scavenging activities

Published:2023-01-03 Issue:5 Volume:77 Page:2581-2604
ISSN:0366-6352
Container-title:Chemical Papers
language:en
Short-container-title:Chem. Pap.

Author:

Haq Israr ul,Ali Irfan,Khan Khalid Mohammed,Chigurupati Sridevi,Habib Atiya,Salar Uzma,Ahmad Manzoor,Konanki Sreenath,Felemban Shatha Ghazi,Taha Muhammad,Haq Zaheer Ul

Funder

Sindh Higher Education Commission

Publisher

Springer Science and Business Media LLC

Subject

Materials Chemistry,Industrial and Manufacturing Engineering,General Chemical Engineering,Biochemistry,General Chemistry

Link

https://link.springer.com/content/pdf/10.1007/s11696-022-02648-5.pdf

Reference71 articles.

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3. Al-Dabbas MM, Kitahara K, Suganuma T, Hashimoto F, Tadera K (2006) Antioxidant and α-amylase inhibitory compounds from aerial parts of varthemia iphionoides boiss. Biosci Biotechnol Biochem 70:2178–2184. https://doi.org/10.1271/bbb.60132

4. Al-Haiza M, Mostafa M, El-Kady M (2003) Synthesis and biological evaluation of some new coumarin derivatives. Molecules 8:275–286. https://doi.org/10.3390/80200275

5. Ali I, Rafique R, Khan KM, Chigurupati S, Ji X, Wadood A, Rehman AU, Salar U, Iqbal MS, Taha M, Perveen S (2020) Potent α-amylase inhibitors and radical (DPPH and ABTS) scavengers based on benzofuran-2-yl (phenyl) methanone derivatives: syntheses, in vitro, kinetics, and in silico studies. Bioorg Chem 104:104238. https://doi.org/10.1016/j.bioorg.2020.104238

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1. Semi-synthesis, α-amylase inhibition, and kinetic and molecular docking studies of arylidene-based sesquiterpene coumarins isolated from Ferula tunetana Pomel ex Batt;RSC Advances;2024