A natural pregnane from Sansevieria hyacinthoides

A study of the steroidal constituents of the leaves of Sansevieria hyacinthoides led to the isolation of 25 S-ruscogenin and a new natural pregnane: 1β, 3β-dihydroxy-5,16-pregnadien-20-one, whose structure was elucidated by spectroscopic methods and confirmed by chemical correlation.

Saved in:
Bibliographic Details
Published inPhytochemistry (Oxford) Vol. 43; no. 5; pp. 1079 - 1081
Main Authors GamboaAngulo, MM, ReyesLopez, J, PenaRodriguez, LM
Format Journal Article
LanguageEnglish
Published OXFORD Elsevier Ltd 01.11.1996
Elsevier
Subjects
Biochemistry & Molecular Biology
Biological and medical sciences
Chemical constitution
Fundamental and applied biological sciences. Psychology
Life Sciences & Biomedicine
Plant physiology and development
Plant Sciences
Science & Technology
Dracenaceae
ruscogenin
Sansevieria hyacinthoides
pregnane
sapogenin
ROOTS
Pregnane derivatives
Steroid
Monocotyledones
Molecular structure
Angiospermae
Sapogenin
Isolation
Agavaceae
Spermatophyta
Plant leaf
Online AccessGet full text

Cover

More Information
Summary:A study of the steroidal constituents of the leaves of Sansevieria hyacinthoides led to the isolation of 25 S-ruscogenin and a new natural pregnane: 1β, 3β-dihydroxy-5,16-pregnadien-20-one, whose structure was elucidated by spectroscopic methods and confirmed by chemical correlation.
ISSN:0031-9422
1873-3700
DOI:10.1016/S0031-9422(96)00409-8