68039-19-0 Usage
Uses
Used in Pharmaceutical Applications:
Alpha-D-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-D-glucopyranuronosyl-, potassium salt is used as a potential biologically active substance for [application reason], given its complex structure and potential interactions with biological systems.
Used in Research and Development:
In the field of organic chemistry and biochemistry, alpha-D-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-D-glucopyranuronosyl-, potassium salt is used as a research compound for [application reason], to explore its chemical properties, potential reactivity, and possible applications in various scientific fields.
Used in Drug Discovery:
alpha-d-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-d-glucopyranuronosyl-, potassium salt is used as a lead molecule in drug discovery for [application reason], due to its unique structure and the possibility of it interacting with biological targets, which could lead to the development of new therapeutic agents.
(Note: The "application reason" should be filled in with specific reasons based on the targeted research and potential applications that have been identified for alpha-d-Glucopyranosiduronic acid, (3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en-3-yl 2-O-beta-d-glucopyranuronosyl-, potassium salt.)
Check Digit Verification of cas no
The CAS Registry Mumber 68039-19-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,3 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68039-19:
(7*6)+(6*8)+(5*0)+(4*3)+(3*9)+(2*1)+(1*9)=140
140 % 10 = 0
So 68039-19-0 is a valid CAS Registry Number.
68039-19-0Relevant 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.