149196-85-0 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-3-AMINO-3-(2-PYRIDINYL)PROPIONIC ACID is utilized as a key component in the synthesis of peptides and pharmaceuticals, leveraging its unique structural features to create novel therapeutic agents.
Used in Neurological Disorder Treatment:
In the medical field, (S)-3-AMINO-3-(2-PYRIDINYL)PROPIONIC ACID is employed as a potential treatment for neurological disorders, owing to its capacity to modulate specific biological pathways and mechanisms associated with such conditions.
Used as a Ligand for GPR18:
(S)-3-AMINO-3-(2-PYRIDINYL)PROPIONIC ACID serves as a ligand for the G protein-coupled receptor 18 (GPR18), playing a significant role in the study and potential therapeutic targeting of this receptor, which is implicated in various physiological and pathological processes.
Used in Drug Delivery System Development:
(S)-3-AMINO-3-(2-PYRIDINYL)PROPIONIC ACID is also harnessed in the development of innovative drug delivery systems, aiming to enhance the efficacy and targeted delivery of pharmaceuticals, thereby improving treatment outcomes.
Used as a Building Block in Organic Synthesis:
In the realm of organic chemistry, (S)-3-AMINO-3-(2-PYRIDINYL)PROPIONIC ACID is valued as a building block, contributing to the creation of new organic compounds with diverse applications in chemical research and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 149196-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,1,9 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 149196-85:
(8*1)+(7*4)+(6*9)+(5*1)+(4*9)+(3*6)+(2*8)+(1*5)=170
170 % 10 = 0
So 149196-85-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O2/c9-6(5-8(11)12)7-3-1-2-4-10-7/h1-4,6H,5,9H2,(H,11,12)/t6-/m0/s1
149196-85-0Relevant academic research and scientific papers
Burkholderia cepacia lipase is an excellent enzyme for the enantioselective hydrolysis of β-heteroaryl-β-amino esters
Tasnadi, Gabor,Forro, Eniko,Fueloep, Ferenc
experimental part, p. 1771 - 1777 (2009/12/28)
The enantioselective (E >200) lipase PS-catalysed hydrolysis of β-heteroaryl-β-amino esters is described. The reactions were performed with H2O (0.5 equiv) in either diisopropyl ether or tert-butyl methyl ether at 25 °C. The resulting β-heteroaryl-substituted β-amino acid enantiomers were formed in high enantiomeric excess (ee ≥ 97%) and in good yield (≥40%).
