110527-69-0 Usage
Description
(S)-2-(((Benzyloxy)carbonyl)amino)-3-((R)-2-oxoindolin-3-yl)propanoic acid is a complex chiral organic compound, characterized by its molecular formula C24H22N2O6. It is an amino acid derivative featuring a benzyl group and an indolin-3-yl group attached to the central propanoic acid moiety. The structural complexity and the presence of these functional groups suggest potential applications in pharmaceuticals or research, particularly in drug design and development due to their possible interactions with proteins and enzymes.
Uses
Used in Pharmaceutical Industry:
(S)-2-(((Benzyloxy)carbonyl)amino)-3-((R)-2-oxoindolin-3-yl)propanoic acid is used as a building block for the development of novel pharmaceutical compounds. Its unique structure and chirality allow for the creation of drugs with specific interactions with biological targets, potentially leading to more effective and selective therapies.
Used in Research and Development:
In the field of research and development, (S)-2-(((benzyloxy)carbonyl)amino)-3-((R)-2-oxoindolin-3-yl)propanoic acid serves as a valuable compound for studying the interactions between small molecules and biological systems. Its structural features can be exploited to understand the binding mechanisms and specificity of various proteins and enzymes, which is crucial for the advancement of drug discovery and design.
Used in Drug Design:
(S)-2-(((Benzyloxy)carbonyl)amino)-3-((R)-2-oxoindolin-3-yl)propanoic acid is used as a key component in the design of new drugs targeting specific protein-protein interactions. The presence of the benzyloxy and indolin-3-yl groups may facilitate the development of molecules with high affinity and selectivity for their intended biological targets, potentially leading to improved therapeutic outcomes.
Used in Enzyme Inhibition Studies:
(S)-2-(((Benzyloxy)carbonyl)amino)-3-((R)-2-oxoindolin-3-yl)propanoic acid can be employed in the study of enzyme inhibition, particularly for enzymes that are involved in various diseases. Its structural complexity and chirality may allow for the development of inhibitors with high specificity, which could be beneficial in the treatment of conditions such as cancer, inflammation, and other diseases where enzyme inhibition plays a crucial role.
Check Digit Verification of cas no
The CAS Registry Mumber 110527-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,5,2 and 7 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 110527-69:
(8*1)+(7*1)+(6*0)+(5*5)+(4*2)+(3*7)+(2*6)+(1*9)=90
90 % 10 = 0
So 110527-69-0 is a valid CAS Registry Number.
110527-69-0Relevant articles and documents
A concise preparation of the non-proteinogenic amino acid l-kynurenine
Kleijn, Laurens H.J.,Müskens, Frederike M.,Oppedijk, Sabine F.,De Bruin, Gerjan,Martin, Nathaniel I.
supporting information, p. 6430 - 6432 (2013/01/15)
A concise and practical preparation of the non-proteinogenic amino acid l-kynurenine is reported. The synthetic approach is scalable and provides ready access to this valuable amino acid in either l- or d-stereochemistry starting from l- or d-tryptophan, respectively. In the optimized procedure, two discreet oxidation steps are applied sequentially to convert the tryptophan indole ring into the keto-aniline moiety contained within the kynurenine side chain.
