2017
DOI: 10.1080/10286020.2017.1342636
|View full text |Cite
|
Sign up to set email alerts
|

Isolation and structure elucidation of halymeniaol, a new antimalarial sterol derivative from the red alga Halymenia floresii

Abstract: A new mono-hydroxy acetylated sterol derivative: 12β-hydroxy-3β, 15α, 16β-triacetoxy-cholest-5-en-7-one (halymeniaol) (1), and cholesterol (2) were isolated from the marine red alga Halymenia floresii. The structure of the compound 1 (halymeniaol) was established from its spectral data, derived from HRMS/MS and 2D NMR. Compound 1 exhibited growth inhibitory activity against chloroquine-resistant Plasmodium falciparum 3D7 strain with an IC of 3.0 μM.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
9
0

Year Published

2018
2018
2024
2024

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 14 publications
(9 citation statements)
references
References 22 publications
0
9
0
Order By: Relevance
“…Crucially, the aglycone, which was isolated from the chloroform fraction, was inactive, suggesting that the two sugars potentiate antiplasmodial activity [175]. The marine red alga Halymenia floresii has produced a new steroid, halymeniaol ( 293 ), which inhibited 3D7 P. falciparum and was not cytotoxic [176]. Chemical reinvestigation of the Caribbean sponge Pandaros acanthifolium has yielded two new steroid glycosides, pandaroside G ( 294 ) and pandaroside G methyl ester ( 295 ).…”
Section: Terpenesmentioning
confidence: 99%
“…Crucially, the aglycone, which was isolated from the chloroform fraction, was inactive, suggesting that the two sugars potentiate antiplasmodial activity [175]. The marine red alga Halymenia floresii has produced a new steroid, halymeniaol ( 293 ), which inhibited 3D7 P. falciparum and was not cytotoxic [176]. Chemical reinvestigation of the Caribbean sponge Pandaros acanthifolium has yielded two new steroid glycosides, pandaroside G ( 294 ) and pandaroside G methyl ester ( 295 ).…”
Section: Terpenesmentioning
confidence: 99%
“…5f ) were isolated from marine alga Halymenia floresii. The former exhibited inhibitory activity against chloroquine-resistant P. falciparum 3D7 strain (IC 50 = 3.0 μmol/L) and was not cytotoxic to RAW 264.7 and N2A cells [49]. Sterols, kaimanol (1) and saringosterol (2) (Fig.…”
Section: Marine-derived Quinones Macrolide Lactones and Sterolmentioning
confidence: 99%
“…Chloroquine-resistant malaria parasite, P. falciparum 3D7 strain was very susceptible to a new mono-hydroxy acetylated sterol derivative, 12β-hydroxy-3β, 15α, 16β-triacetoxy-cholest-5-en-7-one (halymeniaol) (1) (IC 50 = 3.0 µM) produced by an Indian marine red alga, Halymenia Floresii. This is the first sterol derivative (aside cholesterol (2)) isolated from a red alga that is non-cytotoxic and has antimalarial potency [116].…”
Section: Marine-derived Antimicrobial Compounds From Algaementioning
confidence: 99%