z-logo
Premium
New Triterpene Saponins from Herniaria glabra
Author(s) -
Freiler Michaela,
Reznicek Gottfried,
Jurenitsch Johann,
Kubelka Wolfgang,
Schmidt Wolfram,
SchubertZsilavecz Manfred,
Haslinger Ernst,
Reiner Josef
Publication year - 1996
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.19960790207
Subject(s) - chemistry , saponin , triterpene , stereochemistry , two dimensional nuclear magnetic resonance spectroscopy , traditional medicine , medicine , alternative medicine , pathology
Three new saponins 1–3 were isolated from Herniaria glabra by means of prep. HPLC and TLC. The structures were established mainly by a combination of 2D‐NMR techniques (COSY, TOCSY, ROESY, HMQC, and HMBC) as O ‐α‐ L ‐rhamnopyranosyl‐(1→4)‐ O ‐β‐ D ‐glucopyranosyl‐(1‐→6)‐ O ‐[β‐ D ‐glucopyranosyl‐(1→2)]‐β‐ D ‐glucopyranosyl medicagen‐28‐ate (herniaria saponin 4; 1 ), O ‐β‐ D ‐glucopyranosyl‐(1→3)‐ O ‐α‐ L ‐rhamnopyranosyl‐(1→2)‐ O ‐[β‐(3 R )‐ D ‐apiofuranosyl‐(1→3)]‐β‐ D ‐4‐ O ‐acetylfucopyranosyl 3‐ O ‐(β‐ D ‐glucuronopyranosyl)‐16α‐hydroxymedicagen‐28‐ate (herniaria saponin 5; 2 ), and O ‐α‐ L ‐rhamnopyranosyl‐(1→4)‐ O ‐β‐ D ‐glucopyranosyl‐(1→6)‐ O ‐[β‐ D ‐6‐ O ‐acetylglucopyra nosyl‐(1→2)]‐β‐ D ‐glucopyranosyl medicagen‐28‐ate (herniaria saponin 6; 3 ).

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom