30651-43-5 Usage
Uses
Used in Pharmaceutical Industry:
(S)-S-(2-amino-2-carboxyethyl)-D-homocysteine is used as an intermediate in the synthesis of various pharmaceutical compounds for its involvement in the methionine salvage pathway and its role as a precursor to S-adenosylmethionine, which is crucial in methylation reactions and other biochemical processes.
Used in Biochemical Research:
In the field of biochemical research, (S)-S-(2-amino-2-carboxyethyl)-D-homocysteine is utilized as a research tool to study the methionine salvage pathway, the role of S-adenosylmethionine in various cellular processes, and the synthesis and function of coenzyme A in metabolic reactions.
Used in Nutritional Supplements:
(S)-S-(2-amino-2-carboxyethyl)-D-homocysteine may be used as an ingredient in nutritional supplements aimed at supporting the methionine salvage pathway and overall methylation processes in the body, potentially contributing to improved health and well-being.
Used in Diagnostic Applications:
(S)-S-(2-amino-2-carboxyethyl)-D-homocysteine can be employed in the development of diagnostic tools and tests to measure the levels of homocysteine and related metabolites in the body, which can be indicative of various health conditions and the effectiveness of treatments targeting the methionine salvage pathway.
Check Digit Verification of cas no
The CAS Registry Mumber 30651-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,5 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 30651-43:
(7*3)+(6*0)+(5*6)+(4*5)+(3*1)+(2*4)+(1*3)=85
85 % 10 = 5
So 30651-43-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H14N2O4S/c8-4(6(10)11)1-2-14-3-5(9)7(12)13/h4-5H,1-3,8-9H2,(H,10,11)(H,12,13)/t4-,5?/m1/s1
30651-43-5Relevant academic research and scientific papers
Shiraiwa, Tadashi,Nakagawa, Kazuo,Kanemoto, Norito,Kinda, Tomohiro,Yamamoto, Hiroki
, p. 1081 - 1085 (2002)
In order to synthesize four stereoisomers of cystathionine (CYT), D- and L-homocysteines (D- and L-Hcy) were synthesized from methionine (Met) by a facile procedure. L-Met was reacted with dichloroacetic acid in concentrated hydrochloric acid under reflux to give (4S)-1,3-thiazane-2,4-dicarboxylic acid hydrochloride [(4S)-TDC? HCl]. L-Hcy was obtained by treatment of (4S)-TDC? HCl with hydroxylamine. D-Hcy was also synthesized from D-Met via (4R)-TDC? HCl intermediate. The obtained D- and L-Hcy were condensed with (R)- and (S)-2-amino-3-chloropropanoic acid hydrochlorides under alkaline conditions to give four stereoisomers of CYT.
