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Details

Stereochemistry ABSOLUTE
Molecular Formula C42H64O16
Molecular Weight 824.948
Optical Activity ( + )
Defined Stereocenters 20 / 20
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of URALSAPONIN P

SMILES

CC1(C)[C@H](CC[C@@]2(C)[C@H]1CC[C@]3(C)[C@@H]2C(=O)C=C4[C@@H]5C[C@](C)([C@H](O)C[C@]5(C)CC[C@@]34C)C(O)=O)O[C@@H]6O[C@@H]([C@@H](O)[C@H](O)[C@H]6O[C@@H]7O[C@H](CO)[C@H](O)[C@H](O)[C@H]7O)C(O)=O

InChI

InChIKey=RMNUYAJCFQKSFY-CVZCIHLESA-N
InChI=1S/C42H64O16/c1-37(2)22-8-11-42(7)32(20(44)14-18-19-15-40(5,36(53)54)23(45)16-38(19,3)12-13-41(18,42)6)39(22,4)10-9-24(37)56-35-31(28(49)27(48)30(57-35)33(51)52)58-34-29(50)26(47)25(46)21(17-43)55-34/h14,19,21-32,34-35,43,45-50H,8-13,15-17H2,1-7H3,(H,51,52)(H,53,54)/t19-,21+,22-,23+,24-,25-,26-,27-,28-,29+,30-,31+,32+,34-,35+,38-,39-,40+,41+,42+/m0/s1

HIDE SMILES / InChI

Molecular Formula C42H64O16
Molecular Weight 824.948
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 20:56:17 GMT 2025
Edited
by admin
on Mon Mar 31 20:56:17 GMT 2025
Record UNII
PW27SD8M92
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3.BETA.,21.ALPHA.-DIHYDROXY-11-OXO-OLEAN-12-EN-30-OIC ACID(21.ALPHA.-HYDROXYGLYCYRRHETINIC ACID)
Preferred Name English
URALSAPONIN P
Common Name English
.BETA.-D-GLUCOPYRANOSIDURONIC ACID, (3.BETA.,20.BETA.,21.ALPHA.)-20-CARBOXY-21-HYDROXY-11-OXO-30-NOROLEAN-12-EN-3-YL 2-O-.BETA.-D-GALACTOPYRANOSYL-
Systematic Name English
Code System Code Type Description
CAS
1616062-81-7
Created by admin on Mon Mar 31 20:56:17 GMT 2025 , Edited by admin on Mon Mar 31 20:56:17 GMT 2025
PRIMARY
FDA UNII
PW27SD8M92
Created by admin on Mon Mar 31 20:56:17 GMT 2025 , Edited by admin on Mon Mar 31 20:56:17 GMT 2025
PRIMARY
PUBCHEM
162623698
Created by admin on Mon Mar 31 20:56:17 GMT 2025 , Edited by admin on Mon Mar 31 20:56:17 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> CONSTITUENT ALWAYS PRESENT
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.