Adekunle, YA, Samuel, BB, Nahar, L, Fatokun, AA and Sarker, S 
ORCID: 0000-0003-4038-0514
  
(2023)
Cytotoxic triterpenoid saponins from the root of Olax subscorpioidea Oliv. (Olacaceae).
    Phytochemistry: the international journal of plant chemistry, plant biochemistry and molecular biology.
    
     ISSN 0031-9422
  
  
  
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 Cytotoxic triterpenoid saponins from the root of Olax subscorpioidea Oliv. (Olacaceae).pdf - Published Version Available under License Creative Commons Attribution Non-commercial No Derivatives. Download (2MB) | Preview  | 
          
Abstract
Bioactivity-guided phytochemical fractionation of the methanol extract of Olax subscorpioidea root has led to the isolation of six triterpenes. Three of these compounds are previously undescribed triterpenoid saponins: oleanolic acid 3-O-[α-L-rhamnopyranosyl-(1→3)-β-D-glucopyranosyl-(1→2)-6-O-methyl-β-D-glucuronopyranoside]-28-O-β-D-glucopyranosyl ester (2), oleanolic acid 3-O-[β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→3)-β-D-glucopyranoside] (3), and oleanolic acid 3-O-[β-D-glucopyranosyl-(1→4)-6-O-methyl-β-D-glucuronopyranoside] ester (5). Other reported known compounds include two triterpene glycosides: oleanolic acid 3-O-[β-D-glucopyranosyl-(1→4)-6-O-methyl-β-D-glucuronopyranoside]-28-O-β-D-glucopyranosyl ester (1) and oleanolic acid 3-O-[β-D-glucopyranosyl-(1→4)-β-D-glucuronopyranoside] (4); and a triterpene acid, oleanolic acid (6). The structures of these compounds were elucidated by spectroscopic means. The isolated compounds were tested against human cervical cancer (HeLa), colorectal cancer (Caco-2) and breast cancer (MCF-7) cell lines using the in vitro 3-[4,5-dimethylthiazole-2-yl] 3,5-diphenyltetrazolium bromide (MTT) assay, with vincristine as positive control. The cytotoxicity assay showed that compounds 3 and 5 exhibited significant inhibitory effects on the HeLa cell line, with IC50 values of 7.42±0.34 µM and 10.27±1.26 µM; and moderate effects on MCF-7 (IC50 values, 36.67±1.23 µM and 43.83±0.65 µM) and Caco-2 (IC50 values, 35.83±0.55 µM and 39.03±4.38 µM, respectively) cell lines. They were also more selectively cytotoxic than vincristine against the cancer cell lines, when compared with cytotoxicity against the normal lung cell line MRC5.
| Item Type: | Article | 
|---|---|
| Uncontrolled Keywords: | 03 Chemical Sciences; 06 Biological Sciences; 11 Medical and Health Sciences; Plant Biology & Botany | 
| Subjects: | R Medicine > RS Pharmacy and materia medica | 
| Divisions: | Pharmacy and Biomolecular Sciences | 
| Publisher: | Elsevier | 
| Date of acceptance: | 5 September 2023 | 
| Date of first compliant Open Access: | 28 September 2023 | 
| Date Deposited: | 08 Sep 2023 10:01 | 
| Last Modified: | 04 Jul 2025 16:45 | 
| URI: | https://researchonline.ljmu.ac.uk/id/eprint/21289 | 
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