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Natural Product Research
Formerly Natural Product Letters
Volume 36, 2022 - Issue 16
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Research Articles

Triterpenoids from the aerial parts of Anabasis articulata (Forssk) Moq: gastroprotective effect in vivo with in silico studies, cytotoxic and antimicrobial activities

, &
Pages 4076-4084 | Received 12 Jun 2021, Accepted 22 Jul 2021, Published online: 12 Aug 2021
 

Abstract

A new triterpenoid named 3β,20α-dihydroxy-30-nor-olean-12-ene-23,28 dioic acid (4) along with 3β-hydroxy-23-aldehyde-lup-20(29)-ene-28-oic acid (1), 3β-hydroxy-23-aldehyde-30-nor-olean-12,20(29)-diene-28-oic acid (2), 3β-hydroxy-lup-20(29)-ene-23,28 dioic acid (3), 3β-hydroxy-lup-20(29)-ene-23,28 dioic acid-23-O-β-D-glucopyranosyl ester (5), 3-O-β-D-glucuronopyranosyl-lup-20(29)-ene-23,28 dioic acid-28-O-β-D-glucopyranosyl ester (6), 3-O-β-D-glucuronopyranosyl-lup-20(29)-ene-23-aldehyde-28-oic acid-28-O-β-D glucopyranosyl ester (7) were isolated for the first time from the aerial parts of Anabasis articulata (Forssk) Moq. Isolated pure compounds were structurally elucidated using spectral analysis. Cytotoxic, antimicrobial, antiulcer activities and antioxidant parameters were evaluated using the total methanol extract and its successive fractions. The methylene chloride fraction showed strong cytotoxic activity against HepG-2 (6.9 µg/ml) and HCT-116 (5.5 µg/ml) tumour cell lines in comparative with 5-fluorouracil (7.9 µg/ml). Treatment of indomethacin induced ulcerated rats with ethyl acetate fraction (400 mg/kg, p.o./day) achieved reduced Ulcer index (0.18), potent inhibition percentage of ulceration (84.86%) in comparison to ranitidine and high antioxidant effect. Compound(6) exhibited high docking score against gastric H+/K+ ATPase.

Graphical Abstract

Acknowledgement

The authors are grateful to Dr. Abdullah A. Elgazar, teaching assistant, Department of Pharmacognosy, Faculty of Pharmacy, Kafr Elsheikh University for his contribution at our research by molecular docking.

Disclosure statement

No potential conflict of interest was reported by the authors.

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