42294-03-1 Usage
Description
Alpha-d-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-d-glucopyranuronosyl-, monopotassium salt is a complex organic compound derived from the oleanolic acid family. It is characterized by its unique chemical structure, which includes a glucopyranosiduronic acid and a monopotassium salt. alpha-d-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-d-glucopyranuronosyl-, monopotassium salt has potential applications in various industries due to its unique properties and interactions with other molecules.
Uses
Used in Pharmaceutical Industry:
Alpha-d-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-d-glucopyranuronosyl-, monopotassium salt is used as a pharmaceutical compound for its potential therapeutic effects. alpha-d-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-d-glucopyranuronosyl-, monopotassium salt's unique structure allows it to interact with various biological targets, making it a promising candidate for the development of new drugs.
Used in Cosmetic Industry:
In the cosmetic industry, alpha-d-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-d-glucopyranuronosyl-, monopotassium salt is used as an active ingredient for its potential anti-aging and skin-protective properties. alpha-d-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-d-glucopyranuronosyl-, monopotassium salt's ability to interact with biopolymers and macromolecules may contribute to its effectiveness in promoting skin health and reducing the signs of aging.
Used in Research and Development:
Alpha-d-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-d-glucopyranuronosyl-, monopotassium salt is also used in research and development for its potential applications in various fields. Scientists and researchers may utilize this compound to study its interactions with other molecules and to develop new methods for synthesizing and modifying its structure for specific applications.
Note: The provided materials do not mention any specific uses for alpha-d-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-d-glucopyranuronosyl-, monopotassium salt. The uses listed above are hypothetical and based on the compound's potential properties and interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 42294-03-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,9 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42294-03:
(7*4)+(6*2)+(5*2)+(4*9)+(3*4)+(2*0)+(1*3)=101
101 % 10 = 1
So 42294-03-1 is a valid CAS Registry Number.
InChI:InChI=1/C42H62O16.K/c1-37(2)21-8-11-42(7)31(20(43)16-18-19-17-39(4,36(53)54)13-12-38(19,3)14-15-41(18,42)6)40(21,5)10-9-22(37)55-35-30(26(47)25(46)29(57-35)33(51)52)58-34-27(48)23(44)24(45)28(56-34)32(49)50;/h16,19,21-31,34-35,44-48H,8-15,17H2,1-7H3,(H,49,50)(H,51,52)(H,53,54);/q;+1/p-1/t19-,21-,22-,23-,24-,25-,26-,27+,28-,29-,30+,31+,34-,35-,38+,39-,40-,41+,42+;/m0./s1
42294-03-1Relevant articles and documents
TRANSFORMATIONS OF GLYCYRRHIZIC ACID. III.* SYNTHESIS OF NEW GLYCOPEPTIDES CONTAINING METHYL ESTERS OF AMINO ACIDS
Baltina, L. A.,Tolstikov, G. A.
, p. 1115 - 1120 (2007/10/02)
A new selective method has been proposed for the preparation of glycopeptides of β-glycyrrhizic acid (I) containing fragments of methyl esters of amino acids by reacting tris-N-hydroxysuccinimidic ester of a glycoside, obtained in situ using N,N'-dicyclohexylcarbodiimide, with hydrochlorides of methyl esters of amino acids or dipeptides in the presence of triethylamine.
