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J.A. Saliu

Researcher at Adekunle Ajasin University

Publications -  19
Citations -  389

J.A. Saliu is an academic researcher from Adekunle Ajasin University. The author has contributed to research in topics: Rutin & Caffeic acid. The author has an hindex of 7, co-authored 16 publications receiving 310 citations. Previous affiliations of J.A. Saliu include Universidade Federal de Santa Maria & University of Ibadan.

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Inhibitory effect of polyphenol-rich extracts of jute leaf (Corchorus olitorius) on key enzyme linked to type 2 diabetes (α-amylase and α-glucosidase) and hypertension (angiotensin I converting) in vitro

TL;DR: In this paper, the inhibitory action of polyphenol-rich extracts (free and bound) of C. olitorius on α-amylase, α-glucosidase and angiotensin I converting enzyme (ACE), as well as identifying the phenolic compound responsible for these activities were characterized.
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In vitro antidiabetes and antihypertension properties of phenolic extracts from bitter leaf (vernonia amygdalina del.)

TL;DR: In this paper, the authors investigated the inhibitory effect of free and bound phenol extracts of bitter leaf on key enzymes linked to type-2 diabetes (α-glucosidase and α-amylase) and hypertension (angiotensin-I converting enzyme [ACE]).
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Chromatographic Fingerprint Analysis, Acetylcholinesterase Inhibitory Properties and Antioxidant Activities of Redflower Ragleaf (Crassocephalum Crepidioides) Extract

TL;DR: Results reveal that the vegetable extract of redflower ragleaf is a rich source of phenolic compounds with antioxidant and acetylcholinesterase inhibitory potential and may be beneficial for treatment of Alzheimer's disease.
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Comparative Study on the Phenolic Content, Antioxidant Properties and HPLC Fingerprinting of Three Varieties of Celosia Species

TL;DR: In this article, the phenolic content, characterization and antioxidant properties of aqueous extracts of three varieties of Celosia species were assessed and it was shown that the extracts showed strong antioxidant actions as revealed by their 2.2-diphenyl-1-picrylhydrazyl radical, 2,2′-azinobis-3-ethylbenzo-thiazoline-6-sulfonate, nitric oxide radical-scavenging abilities and reducing power.