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Details

Stereochemistry ABSOLUTE
Molecular Formula C30H46O4
Molecular Weight 470.6838
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GYPSOGENIN

SMILES

CC1(C)CC[C@@]2(CC[C@]3(C)C(=CC[C@@H]4[C@@]5(C)CC[C@H](O)[C@@](C)(C=O)[C@@H]5CC[C@@]34C)[C@@H]2C1)C(O)=O

InChI

InChIKey=QMHCWDVPABYZMC-MYPRUECHSA-N
InChI=1S/C30H46O4/c1-25(2)13-15-30(24(33)34)16-14-28(5)19(20(30)17-25)7-8-22-26(3)11-10-23(32)27(4,18-31)21(26)9-12-29(22,28)6/h7,18,20-23,32H,8-17H2,1-6H3,(H,33,34)/t20-,21+,22+,23-,26-,27-,28+,29+,30-/m0/s1

HIDE SMILES / InChI

Molecular Formula C30H46O4
Molecular Weight 470.6838
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
New resistance-correlated saponins from the insect-resistant crucifer Barbarea vulgaris.
2010-05-12
The role of lipid and carbohydrate digestive enzyme inhibitors in the management of obesity: a review of current and emerging therapeutic agents.
2010-05-10
Pancreatic lipase-inhibiting triterpenoid saponins from fruits of Acanthopanax senticosus.
2007-07
Pancreatic lipase-inhibiting triterpenoid saponins from Gypsophila oldhamiana.
2007-04
Four new triterpene glycosides from Nigella damascena.
2007-03
Analysis of gypsogenin saponins in homeopathic tinctures.
2007
Analysis of bisdesmosidic saponins in Saponaria vaccaria L. by HPLC-PAD-MS: identification of new quillaic acid and gypsogenin 3-O-trisaccharides.
2006-12-06
Bioactive flavonoids and saponins from Climacoptera obtusifolia.
2006-11
Triterpenoid saponins from the fruits of Akebiae quinata.
2006-05
A new adaptive subband decomposition approach for automatic analysis of NMR data.
2004-07
Triterpenoid saponins from the roots of Silene cucubalus.
2003-04
Studies on the constituents of Clematis species. VIII. Triterpenoid saponins from the aerial part of Clematis tibetana KUNTZ.
2001-05
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:47:00 GMT 2025
Edited
by admin
on Mon Mar 31 21:47:00 GMT 2025
Record UNII
2A9SGC905J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(3.BETA.,4.ALPHA.)-3-HYDROXY-23-OXOOLEAN-12-EN-28-OIC ACID
Preferred Name English
GYPSOGENIN
MI  
Common Name English
OLEAN-12-EN-28-OIC ACID, 3-HYDROXY-23-OXO-, (3.BETA.,4.ALPHA.)-
Systematic Name English
ALBSAPOGENIN
Common Name English
GITHAGENIN
Common Name English
GYPSOPHILASAPOGENIN
Common Name English
GYPSOGENIN [MI]
Common Name English
ASTRANTIAGENIN D
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID701026577
Created by admin on Mon Mar 31 21:47:00 GMT 2025 , Edited by admin on Mon Mar 31 21:47:00 GMT 2025
PRIMARY
CHEBI
5580
Created by admin on Mon Mar 31 21:47:00 GMT 2025 , Edited by admin on Mon Mar 31 21:47:00 GMT 2025
PRIMARY
CHEBI
140467
Created by admin on Mon Mar 31 21:47:00 GMT 2025 , Edited by admin on Mon Mar 31 21:47:00 GMT 2025
PRIMARY
PUBCHEM
92825
Created by admin on Mon Mar 31 21:47:00 GMT 2025 , Edited by admin on Mon Mar 31 21:47:00 GMT 2025
PRIMARY
FDA UNII
2A9SGC905J
Created by admin on Mon Mar 31 21:47:00 GMT 2025 , Edited by admin on Mon Mar 31 21:47:00 GMT 2025
PRIMARY
ECHA (EC/EINECS)
211-353-7
Created by admin on Mon Mar 31 21:47:00 GMT 2025 , Edited by admin on Mon Mar 31 21:47:00 GMT 2025
PRIMARY
CAS
639-14-5
Created by admin on Mon Mar 31 21:47:00 GMT 2025 , Edited by admin on Mon Mar 31 21:47:00 GMT 2025
PRIMARY
MERCK INDEX
m224
Created by admin on Mon Mar 31 21:47:00 GMT 2025 , Edited by admin on Mon Mar 31 21:47:00 GMT 2025
PRIMARY Merck Index