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

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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),… Click to show full 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.

Keywords: lup ene; dioic acid; ene; acid; aerial parts; ene dioic

Journal Title: Natural product research
Year Published: 2021

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