174879-28-8 Usage
Uses
Used in Pharmaceutical and Biochemical Research:
FMOC-DL-2-AMINOBUTYRIC ACID is used as a synthetic building block for the creation of custom peptides and proteins. Its incorporation allows researchers to study the effects of specific amino acid sequences on protein function and stability.
Used in Chemical Biology:
FMOC-DL-2-AMINOBUTYRIC ACID is utilized as a component in the design of bioactive molecules, facilitating the exploration of protein-ligand interactions and the development of novel biological probes.
Used in Drug Discovery:
In the quest for new therapeutic agents, FMOC-DL-2-AMINOBUTYRIC ACID is employed as a key constituent in the synthesis of peptide-based drugs, potentially leading to the discovery of medicines with improved pharmacological properties.
Used in Protein Engineering:
FMOC-DL-2-AMINOBUTYRIC ACID is used as a modifying agent in protein engineering, enabling the alteration of protein properties such as folding, stability, and activity, which is vital for the creation of proteins with tailored functions for various applications.
Used in Peptide Synthesis Education:
FMOC-DL-2-AMINOBUTYRIC ACID serves as an educational tool in teaching laboratories, where students learn about the principles of peptide synthesis and the role of protecting groups in the process.
Check Digit Verification of cas no
The CAS Registry Mumber 174879-28-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,8,7 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 174879-28:
(8*1)+(7*7)+(6*4)+(5*8)+(4*7)+(3*9)+(2*2)+(1*8)=188
188 % 10 = 8
So 174879-28-8 is a valid CAS Registry Number.
InChI:InChI=1/C19H19NO4/c1-2-17(18(21)22)20-19(23)24-11-16-14-9-5-3-7-12(14)13-8-4-6-10-15(13)16/h3-10,16-17H,2,11H2,1H3,(H,20,23)(H,21,22)/p-1/t17-/m1/s1
174879-28-8Relevant academic research and scientific papers
O'Donnell, Martin J.,Delgado, Francisca,Drew, Mark D.,Pottorf, Richard S.,Zhou, Changyou,Scott, William L.
, p. 5831 - 5835 (1999)
Unnatural amino acids were synthesized on solid-phase by reaction of a resin-bound Schiff base with organoboranes. This novel use of a resin-bound glycine cation equivalent allows for the preparation of a variety of amino acid structural types not readily available by the complementary anionic equivalent.
Dehydration of threonine esters during tosylation
Somlai,Lovas,Forgo,Murphy,Penke
, p. 3633 - 3640 (2007/10/03)
Tosylation of N-α-protected threonine methyl-and benzyl esters was investigated. Depending on the protecting groups, the composition of the reaction mixtures showed different ratio between O-tosyl-and dehydrothreonine derivatives. The latter was formed ex
Fibrinogen receptor antagonist and pharmaceutical compositions comprising the same
-
, (2008/06/13)
Compounds of the following general formula (I) and pharmaceutically acceptable salts thereof.
