URALSAPONIN U

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C42H62O17
Molecular Weight	838.9315
Optical Activity	( + )
Defined Stereocenters	20 / 20
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

C[C@]12CC[C@](C)(C[C@H]1C3=CC(=O)[C@@H]4[C@@]5(C)CC[C@H](O[C@@H]6O[C@@H]([C@@H](O)[C@H](O)[C@H]6O[C@@H]7O[C@@H]([C@@H](O)[C@H](O)[C@H]7O)C(O)=O)C(O)=O)[C@](C)(CO)[C@@H]5CC[C@@]4(C)[C@]3(C)CC2)C(O)=O

InChI

InChIKey=WBQVRPYEEYUEBQ-ZZRFBVNQSA-N

InChI=1S/C42H62O17/c1-37-11-12-38(2,36(54)55)16-19(37)18-15-20(44)31-39(3)9-8-22(40(4,17-43)21(39)7-10-42(31,6)41(18,5)14-13-37)56-35-30(26(48)25(47)29(58-35)33(52)53)59-34-27(49)23(45)24(46)28(57-34)32(50)51/h15,19,21-31,34-35,43,45-49H,7-14,16-17H2,1-6H3,(H,50,51)(H,52,53)(H,54,55)/t19-,21+,22-,23-,24-,25-,26-,27+,28-,29-,30+,31+,34-,35+,37+,38+,39-,40+,41+,42+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C42H62O17
Molecular Weight	838.9315
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	20 / 20
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 20:56:18 GMT 2025` Edited by `admin` on `Mon Mar 31 20:56:18 GMT 2025`
Record UNII	HT2MUA8H8Z
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

24-HYDROXY-20.ALPHA.-GLYCYRRHIZIN

Preferred Name

English

URALSAPONIN U

Common Name

English

3.BETA.-O-(.BETA.-DGLUCURONOPYRANOSYL-(1->2)-.BETA.-D-GLUCURONOPYRANOSYL)-24-HYDROXY-11-OXO-OLEAN-12-EN-29-OIC ACID

Common Name

English

.BETA.-D-GLUCOPYRANOSIDURONIC ACID, (3.BETA.,4.BETA.,20.ALPHA.)-20-CARBOXY-23-HYDROXY-11-OXO-30-NOROLEAN-12-EN-3-YL 2-O-.BETA.-D-GLUCOPYRANURONOSYL-

Systematic Name

English

Code System Code Type Description

FDA UNII

HT2MUA8H8Z

Created by admin on Mon Mar 31 20:56:18 GMT 2025 , Edited by admin on Mon Mar 31 20:56:18 GMT 2025

PRIMARY

CAS

1616062-86-2

Created by admin on Mon Mar 31 20:56:18 GMT 2025 , Edited by admin on Mon Mar 31 20:56:18 GMT 2025

PRIMARY

PUBCHEM

162368379

Created by admin on Mon Mar 31 20:56:18 GMT 2025 , Edited by admin on Mon Mar 31 20:56:18 GMT 2025

PRIMARY

Related Record Type Details


					42B5YD8F0K

GLYCYRRHIZA URALENSIS ROOT

PARENT -> CONSTITUENT ALWAYS PRESENT

Comments:

The compound did not show significant cytotoxicity against uninfected MDCK cells at 100 uM, but showed inhibitory activity against the H1N1 virus at 100 uM. The compound was also evaluated for anti-HIV activity.

Amount: