Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

348147

Sigma-Aldrich

Sarsasapogenin

95%

Synonym(s):

(25S)-Spirostan-3β-ol, Parigenin

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C27H44O3
CAS Number:
126-19-2
Molecular Weight:
416.64
MDL number:
MFCD00270414
UNSPSC Code:
12352200
PubChem Substance ID:
329755058

Assay

95%

form

solid

SMILES string

C[C@H]1CC[C@@]2(OC1)O[C@H]3C[C@H]4[C@@H]5CC[C@@H]6C[C@@H](O)CC[C@]6(C)[C@H]5CC[C@]4(C)[C@H]3[C@@H]2C

InChI

1S/C27H44O3/c1-16-7-12-27(29-15-16)17(2)24-23(30-27)14-22-20-6-5-18-13-19(28)8-10-25(18,3)21(20)9-11-26(22,24)4/h16-24,28H,5-15H2,1-4H3/t16-,17-,18+,19-,20+,21-,22-,23-,24-,25-,26-,27+/m0/s1

InChI key

GMBQZIIUCVWOCD-WWASVFFGSA-N

Looking for similar products? Visit Product Comparison Guide

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
07202HW

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Yaer Hu et al.
Neurobiology of aging, 31(6), 1010-1019 (2008-08-05)
The purpose of this work is to study the effect of smilagenin on the mRNA stability of muscarinic receptor subtype 1 (M(1); m1 mRNA) in aged rat brains and its significance in improving memory. The Y-maze avoidance task showed that
Haiyan Hu et al.
FEBS letters, 584(8), 1549-1552 (2010-03-11)
This work studied the role of cyclic AMP responsive element binding protein (CREB) in the up-regulation of M(1) muscarinic acetylcholine receptor (M(1) receptor) density by sarsasapogenin (ZMS) in CHO cells transfected with M(1) receptor gene (CHOm1 cells). During cell aging
Bertrand Liagre et al.
International journal of molecular medicine, 20(4), 451-460 (2007-09-06)
We conducted our study to assess the antiproliferative and proapoptotic potential of hecogenin and tigogenin, two saponins which are structurally similar to diosgenin. We particularly focused our attention on mitogen-activated protein kinase (MAPK) activation in relation to apoptosis but also
Xue-Feng Huang et al.
Journal of integrative plant biology, 50(6), 717-722 (2008-08-21)
One new (Sarsasapogenin O) and seven known steroids were isolated from the roots of Asparagus officinalis L. Their structures were elucidated on the basis of spectroscopic analysis, including various 2D-NMR techniques, hydrolysis, and by comparison of spectral data of known
Jing Wang et al.
Acta pharmacologica Sinica, 31(8), 984-989 (2010-08-06)
To generate a polyclonal antibody against sarsasapogenin and to develop an indirect competitive enzyme-linked immunosorbent assay (IC-ELISA) method for the pharmacokinetic study of Sarsasapogenin in rats. The antigen of sarsasapogenin was produced using an active ester method and subsequently used
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service