25460-87-1 Usage
Description
AC-GLU-NH2, also known as N-Acetyl-L-isoglutamine, is the N-Acetyl analogue of L-isoglutamine, an isomer of the non-essential amino acid L-glutamine. It is a modified form of L-glutamine with an acetyl group attached to the nitrogen atom, which may confer unique properties and potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
AC-GLU-NH2 is used as a pharmaceutical compound for its potential therapeutic effects. The N-Acetyl modification may enhance the stability and bioavailability of the molecule, making it a promising candidate for drug development.
Used in Nutritional Supplements:
AC-GLU-NH2 is used as a nutritional supplement to support overall health and well-being. The N-Acetyl group may improve the absorption and utilization of the compound, providing benefits such as enhanced immune function and muscle recovery.
Used in Cosmetics Industry:
AC-GLU-NH2 is used as an ingredient in cosmetic products for its potential skin benefits. The N-Acetyl modification may provide enhanced hydration and skin barrier function, contributing to healthier and more youthful-looking skin.
Used in Research Applications:
AC-GLU-NH2 is used in research settings to study the effects of N-Acetyl modifications on amino acid function and metabolism. This knowledge can help in the development of new therapeutic agents and a better understanding of amino acid biology.
Check Digit Verification of cas no
The CAS Registry Mumber 25460-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,6 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25460-87:
(7*2)+(6*5)+(5*4)+(4*6)+(3*0)+(2*8)+(1*7)=111
111 % 10 = 1
So 25460-87-1 is a valid CAS Registry Number.
25460-87-1Relevant articles and documents
Two-Step Synthesis of α-Aryl-α-diazoamides as Modular Bioreversible Labels
Jun, Joomyung V.,Raines, Ronald T.
supporting information, p. 3110 - 3114 (2021/05/04)
α-Aryl-α-diazoamides were synthesized in two steps under mild conditions. This expeditious route employs Pd-catalyzed C-H arylation of N-succinimidyl 2-diazoacetate to obtain N-succinimidyl 2-aryl-2-diazoacetates, followed by aminolysis. The ensuing diazo compounds can esterify carboxyl groups in aqueous solution, and the ester products are substrates for an esterase. The broad scope of the synthetic route enables the continued development of diazo compounds in chemical biology.
