U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C36H62O9
Molecular Weight 638.8721
Optical Activity UNSPECIFIED
Defined Stereocenters 16 / 16
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GINSENOSIDE RH1, (20S)-

SMILES

[H][C@@]1(CC[C@]2(C)[C@]1([H])[C@H](O)C[C@]3([H])[C@@]4(C)CC[C@H](O)C(C)(C)[C@]4([H])[C@H](C[C@@]23C)O[C@]5([H])O[C@H](CO)[C@@H](O)[C@H](O)[C@H]5O)[C@@](C)(O)CCC=C(C)C

InChI

InChIKey=RAQNTCRNSXYLAH-RFCGZQMISA-N
InChI=1S/C36H62O9/c1-19(2)10-9-13-36(8,43)20-11-15-34(6)26(20)21(38)16-24-33(5)14-12-25(39)32(3,4)30(33)22(17-35(24,34)7)44-31-29(42)28(41)27(40)23(18-37)45-31/h10,20-31,37-43H,9,11-18H2,1-8H3/t20-,21+,22-,23+,24+,25-,26-,27+,28-,29+,30-,31+,33+,34+,35+,36-/m0/s1

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Ginsenoside Rh1 suppresses inducible nitric oxide synthase gene expression in IFN-gamma-stimulated microglia via modulation of JAK/STAT and ERK signaling pathways.
2010 Jun 25
Ameliorative effects of Compound K and ginsenoside Rh1 on non-alcoholic fatty liver disease in rats.
2017 Jan 20
Preparation and evaluation of self-microemulsions for improved bioavailability of ginsenoside-Rh1 and Rh2.
2017 Oct
Ginsenoside Rh1: A Systematic Review of Its Pharmacological Properties.
2018 Feb
Suppressive Effects of Ginsenoside Rh1 on HMGB1-Mediated Septic Responses.
2019
Name Type Language
GINSENOSIDE RH1, (20S)-
Common Name English
.BETA.-D-GLUCOPYRANOSIDE, (3.BETA.,6.ALPHA.,12.BETA.)-3,12,20-TRIHYDROXYDAMMAR-24-EN-6-YL
Common Name English
SANCHINOSIDE RH1
Common Name English
PROSAPOGENIN A2
Common Name English
GINSENOSIDE RH1
INCI  
Official Name English
20(S)-GINSENOSIDE RH1
Common Name English
S-GINSENOSIDE RH1
Common Name English
SANCHINOSIDE B2
Common Name English
Code System Code Type Description
FDA UNII
XBR6F7G8FU
Created by admin on Sat Dec 16 20:01:25 GMT 2023 , Edited by admin on Sat Dec 16 20:01:25 GMT 2023
PRIMARY
CAS
63223-86-9
Created by admin on Sat Dec 16 20:01:25 GMT 2023 , Edited by admin on Sat Dec 16 20:01:25 GMT 2023
PRIMARY
PUBCHEM
12855920
Created by admin on Sat Dec 16 20:01:25 GMT 2023 , Edited by admin on Sat Dec 16 20:01:25 GMT 2023
PRIMARY
EPA CompTox
DTXSID80979245
Created by admin on Sat Dec 16 20:01:25 GMT 2023 , Edited by admin on Sat Dec 16 20:01:25 GMT 2023
PRIMARY