848396-10-1 Usage
Uses
Used in Pharmaceutical Development:
3-(N-Ethanolamino)-L-alanine is used as a potential drug target for the treatment of certain diseases, particularly cancer, due to its anti-inflammatory and cytotoxic properties. Its role in the biosynthesis of bioactive natural products and its presence in marine organisms highlight its potential for therapeutic applications.
Used in Cancer Treatment:
3-(N-Ethanolamino)-L-alanine is used as a therapeutic agent for cancer treatment, leveraging its cytotoxic properties to target and eliminate cancer cells. Further research is needed to fully understand its therapeutic potential and possible applications in medicine, including its synergistic effects with other treatments and its impact on various types of cancer.
Used in Anti-Inflammatory Applications:
3-(N-Ethanolamino)-L-alanine is used as an anti-inflammatory agent, potentially beneficial in the treatment of conditions characterized by inflammation. Its anti-inflammatory properties may contribute to the management of inflammatory diseases and disorders, although more research is required to determine its full potential in this area.
Used in Marine Biotechnology:
3-(N-Ethanolamino)-L-alanine is used in marine biotechnology for the exploration of its role in the biosynthesis of bioactive natural products. Its presence in marine organisms makes it a valuable compound for studying marine-derived bioactive compounds and their potential applications in medicine and other industries.
Check Digit Verification of cas no
The CAS Registry Mumber 848396-10-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,3,9 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 848396-10:
(8*8)+(7*4)+(6*8)+(5*3)+(4*9)+(3*6)+(2*1)+(1*0)=211
211 % 10 = 1
So 848396-10-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H9N3O2/c7-5(6(10)11)3-9-2-1-8-4-9/h1-2,4-5H,3,7H2,(H,10,11)/t5-/m1/s1
848396-10-1Relevant academic research and scientific papers
Belokon, , Yuri N.,Sagyan, Ashot S.,Djamgaryan, Silva M.,Bakhmutov, Vladimir I.,Belikov, Vasili M.
, p. 5507 - 5514 (1988)
An efficient approach to the asymmetric synthesis of β-substituted (S)-alanines is describen.The chiral Ni(II) complex of a Schiff base derived from (S)-o-N-(N-benzylpropyl)aminobenzophenone (BBP) and glycine was treated with formaldehyde and sodium methoxide to give a corresponding (R)-serine complex which, in turn, was converted to the chiral Ni(II) dehydroalanine complex.Michael type base catalyzed addition of nucleophiles (including MeOH, Me2NH, PhCH2NH2, imidazole, PhSH, PhCH2SH,, malonic ester and benzylmagnesium chloride) produced a mixture of diastereoisomeric complexes with a 70-90percent excess of S,S (or L,L) isomers over the S,R (or L,D) ones.The cleavage of pure diastereoisomers with aqueous HCl gave, in good yields, β-substituted (S) (or L)-alanines and regenerated the chiral auxiliary (BBP).
