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Design, synthesis, molecular docking study, and α-glucosidase inhibitory evaluation of novel hydrazi...

Design, synthesis, molecular docking study, and α-glucosidase inhibitory evaluation of novel hydrazi...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_5b9e13ea75d7412c9a071a48508f6ac4

Design, synthesis, molecular docking study, and α-glucosidase inhibitory evaluation of novel hydrazide–hydrazone derivatives of 3,4-dihydroxyphenylacetic acid

About this item

Full title

Design, synthesis, molecular docking study, and α-glucosidase inhibitory evaluation of novel hydrazide–hydrazone derivatives of 3,4-dihydroxyphenylacetic acid

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2024-05, Vol.14 (1), p.11410-11410, Article 11410

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

A series of novel Schiff base derivatives
(1–28)
of 3,4-dihydroxyphenylacetic acid were synthesized in a multi-step reaction. All the synthesized Schiff bases were obtained in high yields and their structures were determined by
1
HNMR,
13
CNMR, and HR-ESI–MS spectroscopy. Except for compounds
22
,
26
,
27,
and

Alternative Titles

Full title

Design, synthesis, molecular docking study, and α-glucosidase inhibitory evaluation of novel hydrazide–hydrazone derivatives of 3,4-dihydroxyphenylacetic acid

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_5b9e13ea75d7412c9a071a48508f6ac4

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_5b9e13ea75d7412c9a071a48508f6ac4

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/s41598-024-62034-x

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