URALSAPONIN W

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C42H62O15
Molecular Weight	806.9327
Optical Activity	UNSPECIFIED
Defined Stereocenters	19 / 19
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

C[C@@]1(CC[C@]2(C)CC[C@]3(C)C(=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)(C)[C@@H]5CC[C@@]34C)[C@@H]2C1)C=O

InChI

InChIKey=BBTZPUQIJXVLFI-HXBRCTIJSA-N

InChI=1S/C42H62O15/c1-37(2)22-8-11-42(7)32(21(44)16-19-20-17-38(3,18-43)12-13-39(20,4)14-15-41(19,42)6)40(22,5)10-9-23(37)54-36-31(27(48)26(47)30(56-36)34(52)53)57-35-28(49)24(45)25(46)29(55-35)33(50)51/h16,18,20,22-32,35-36,45-49H,8-15,17H2,1-7H3,(H,50,51)(H,52,53)/t20-,22-,23-,24-,25-,26-,27-,28+,29-,30-,31+,32+,35-,36+,38-,39+,40-,41+,42+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C42H62O15
Molecular Weight	806.9327
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	19 / 19
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:52:53 GMT 2025` Edited by `admin` on `Mon Mar 31 21:52:53 GMT 2025`
Record UNII	L8QT245VO6
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

3.BETA.-O-(.BETA.-D-GLUCURONOPYRANOSYL-(1->2)-.BETA.-D-GLUCURONOPYRANOSYL)GLYCYRRHETALDEHYDE

Preferred Name

English

URALSAPONIN W

Common Name

English

.BETA.-D-GLUCOPYRANOSIDURONIC ACID, (3.BETA.,20.BETA.)-11,29-DIOXOOLEAN-12-EN-3-YL 2-O-.BETA.-D-GLUCOPYRANURONOSYL-

Systematic Name

English

Code System Code Type Description

CAS

1616062-88-4

Created by admin on Mon Mar 31 21:52:53 GMT 2025 , Edited by admin on Mon Mar 31 21:52:53 GMT 2025

PRIMARY

FDA UNII

L8QT245VO6

Created by admin on Mon Mar 31 21:52:53 GMT 2025 , Edited by admin on Mon Mar 31 21:52:53 GMT 2025

PRIMARY

PUBCHEM

86278365

Created by admin on Mon Mar 31 21:52:53 GMT 2025 , Edited by admin on Mon Mar 31 21:52:53 GMT 2025

PRIMARY

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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.