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Jean Duplex Wansi

Researcher at University of Douala

Publications -  84
Citations -  864

Jean Duplex Wansi is an academic researcher from University of Douala. The author has contributed to research in topics: Chemistry & Medicine. The author has an hindex of 14, co-authored 67 publications receiving 645 citations. Previous affiliations of Jean Duplex Wansi include Bielefeld University & Liverpool John Moores University.

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α-Glucosidase inhibitory pentacyclic triterpenes from the stem bark of Fagara tessmannii (Rutaceae)

TL;DR: In addition to fatty acids, a mixture of sterols, lupeol, arctigenin methylether, sesamin, vanillic acid, 2,6-dimethoxy-1,4-benzoquinone, betulinic acid and two pentacyclic triterpene acetates were isolated from Fagara tessmannii Engl.
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α-Glucosidase inhibitory constituents from stem bark of Terminalia superba (Combretaceae)

TL;DR: The CH(2)Cl(2)/CH(3)OH (1/1) extract of the dried stem bark of Terminalia superba afforded two compounds, (7S,8R, 7'R,8'S)-4'-hydroxy-4-methoxy-7,7'-epoxylignan and meso-(rel 7S, 8R,7'R-8' S)-4,4'-dimethoxy
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Alpha-glucosidase inhibitory and antioxidant acridone alkaloids from the stem bark of Oriciopsis glaberrima ENGL. (Rutaceae).

TL;DR: The CH2Cl2/MeOH extract of the stem bark of Oriciopsis glaberrima ENGL. afforded four new acridone alkaloids namely oriciacridone C, D, E and F along with six known compounds: atalaphyllidine, oleanolic acid, butulinic acid, beta-sitosterol, stigmasterol, glucoside of stig masterol and one synthetically known acridones: 1,3,5-trihydroxy-4-prenylacridone as mentioned in this paper
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Antimicrobial Furoquinoline Alkaloids from Vepris lecomteana (Pierre) Cheek & T. Heller (Rutaceae).

TL;DR: Three new prenylated furoquinoline alkaloids named lecomtequinoline A, B, and C are isolated by bioassay-guided fractionation of the methanolic extracts of leaves and stem of Vepris lecomeana, suggesting synergistic effect.
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Antiplasmodial activities of furoquinoline alkaloids from Teclea afzelii.

TL;DR: The antimalarial activity of compounds 1–4 against Plasmodium falciparum in vitro shows partial suppression of parasitic growth.