URALSAPONIN M

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C44H64O18
Molecular Weight	880.9682
Optical Activity	( + )
Defined Stereocenters	20 / 20
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

[H][C@@]7(O[C@@H]1[C@@H](O)[C@H](O)[C@H](O[C@@]1([H])O[C@H]2CC[C@@]3(C)[C@@]([H])(CC[C@]4(C)[C@]3([H])C(=O)C=C5[C@]6([H])C[C@](C)(C[C@@H](OC(C)=O)[C@]6(C)CC[C@@]45C)C(O)=O)C2(C)C)C(O)=O)O[C@@H]([C@H](O)[C@H](O)[C@H]7O)C(O)=O

InChI

InChIKey=OBFDSOYVKVRFGY-JEHLDPHZSA-N

InChI=1S/C44H64O18/c1-18(45)58-24-17-40(4,38(56)57)16-20-19-15-21(46)33-42(6)11-10-23(39(2,3)22(42)9-12-44(33,8)43(19,7)14-13-41(20,24)5)59-37-32(28(50)27(49)31(61-37)35(54)55)62-36-29(51)25(47)26(48)30(60-36)34(52)53/h15,20,22-33,36-37,47-51H,9-14,16-17H2,1-8H3,(H,52,53)(H,54,55)(H,56,57)/t20-,22-,23-,24+,25-,26+,27-,28-,29+,30-,31-,32+,33+,36-,37+,40+,41+,42-,43+,44+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C44H64O18
Molecular Weight	880.9682
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 `Sat Dec 16 01:54:27 UTC 2023` Edited by `admin` on `Sat Dec 16 01:54:27 UTC 2023`
Record UNII	SY5TBS2UJ6
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

URALSAPONIN M

Common Name

English

3.BETA.-O-(.BETA.-D-GALACTURONOPYRANOSYL-(1->2)-.BETA.-D-GLUCURONOPYRANOSYL)- 22.BETA.-ACETOXY-11-OXO-OLEAN-12-EN-30-OIC ACID

Common Name

English

.BETA.-D-GLUCOPYRANOSIDURONIC ACID, (3.BETA.,20.BETA.,22.BETA.)-22-(ACETYLOXY)-20-CARBOXY-11-OXO-30-NOROLEAN-12-EN-3-YL 2-O-.BETA.-D-GALACTOPYRANURONOSYL-

Systematic Name

English

Code System Code Type Description

CAS

1616062-78-2

Created by admin on Sat Dec 16 01:54:27 UTC 2023 , Edited by admin on Sat Dec 16 01:54:27 UTC 2023

PRIMARY

PUBCHEM

162623962

Created by admin on Sat Dec 16 01:54:27 UTC 2023 , Edited by admin on Sat Dec 16 01:54:27 UTC 2023

PRIMARY

FDA UNII

SY5TBS2UJ6

Created by admin on Sat Dec 16 01:54:27 UTC 2023 , Edited by admin on Sat Dec 16 01:54:27 UTC 2023

PRIMARY

Related Record Type Details


					42B5YD8F0K

GLYCYRRHIZA URALENSIS ROOT

PARENT -> CONSTITUENT ALWAYS PRESENT

Comments:

Anti-H1N1 (IC50 in uM) activity of compound was shown to be 48.0 uM. 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: