EventsThe 2nd International Electronic Conference on Diversity
Published
with-doi10.3390/IECD2022-12417 (registering DOI)
This submission belongs to the session A. Animals Diversity of the event The 2nd International Electronic Conference on Diversity
Published date
15 Mar, 2022
Academic Editor
author-avatarMatthieu Chauvat
Citation
Juan Enrique Tacoronte Morales, Joseph Cruel Sigüenza, María Elizabeth Canchingre, Carla Bernal Villavicencio, Lanostane triol (holothurin group) isolated from triterpenic fraction of Holothuria floridana inhabiting in shallow waters of Cuban Archipelago, in Proceedings of The 2nd International Electronic Conference on Diversity, 15 March–31 March 2022, MDPI: Basel, Switzerland, doi: 10.3390/IECD2022-12417
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Lanostane triol (holothurin group) isolated from triterpenic fraction of Holothuria floridana inhabiting in shallow waters of Cuban Archipelago

Joseph Cruel Sigüenza 2
María Elizabeth Canchingre 2
Carla Bernal Villavicencio 2
1. Technical University of Esmeraldas. Campus New Horizons. Faculty of Science & Technology, Chemical En-gineering Coordination. Esmeraldas, Republic of Ecuador, China
2. Technical University of Esmeraldas. Campus New Horizons. Faculty of Science & Technology, Chemical En-gineering Coordination. Esmeraldas, Republic of Ecuador
Abstract

Holothurians (Echinodermata, Aspirochirotida, Holothuridae, Holothuria) are marine epibenthic organisms with a wide geographical distribution which are used for human consumption. They have an extraordinary variety of metabolites, specifically triterpenic glycosides of the holostane type (lanostane). The present work is intended to develop a preliminary chemical study of holothurians (sea cucumbers) that inhabit the shallow waters of the south-western marine insular platform of Cuba and report a preliminary structural detail of a triterpenic holostanic glycoside isolated from methanolic extracts of Holothuria floridana. A triterpene glycoside fraction was separated chromatographically on Amberlite and was isolated as a triterpene glycoside. Its structure has been deduced, from spectral analysis (NMR, FTIR) and chromogenic reactions. The compound is an open-chain, holost-Δ9,11-en-12α,17α,22ξ triol tetraoside, belonging to the group A of the holoturins, which possesses 3β-D-glucose, D-xylose, D-quinovose and 3-O-methyl-D-glucose as monosaccharide fragments.

Keywords
Holothuria floridana
triterpene glycoside
holothurin
monosaccharides
chromogenic reactions
Manuscript
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