2382-80-1 Usage
Description
AC-TRP-OET, also known as N-Acetyl-L-tryptophan ethyl ester, is a synthetic compound derived from the combination of N-Acetyl-L-tryptophan and ethyl ester. It is a white to slightly cream crystalline powder with unique chemical properties that make it suitable for various applications.
Uses
Used in Pharmaceutical Industry:
AC-TRP-OET is used as a substrate for enzymes such as chymotrypsin and carboxypeptidase Y. Its role in the pharmaceutical industry is to aid in the study and development of drugs targeting these enzymes, which are involved in various biological processes and diseases.
Used in Research and Development:
AC-TRP-OET serves as a valuable compound for research and development purposes. Its unique chemical properties allow scientists to investigate its interactions with different enzymes and proteins, potentially leading to the discovery of new therapeutic agents and applications in the medical field.
Used in Quality Control:
In the pharmaceutical industry, AC-TRP-OET can be used as a reference material for quality control purposes. Its consistent chemical properties make it an ideal candidate for ensuring the accuracy and reliability of analytical methods and assays used in the development and production of drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 2382-80-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2382-80:
(6*2)+(5*3)+(4*8)+(3*2)+(2*8)+(1*0)=81
81 % 10 = 1
So 2382-80-1 is a valid CAS Registry Number.
InChI:InChI=1/C15H18N2O3/c1-3-20-15(19)14(17-10(2)18)8-11-9-16-13-7-5-4-6-12(11)13/h4-7,9,14,16H,3,8H2,1-2H3,(H,17,18)/t14-/m0/s1
2382-80-1Relevant articles and documents
The retro-mannich cleavage of δ1,δ1'-tryptophan dimers
Biggs, Bluegrass,Presley, Alice L.,Van Vranken, David L.
, p. 975 - 981 (1998)
Under acidic conditions tryptophan sidechains crosslink to form δ1, δ1'-tryptophan dimers through a Mannich-type mechanism. Tryptophan dimers are readily cleaved at high temperatures under acidic conditions making it impossible to isolate tryptophan dimers under standard conditions of acidic protein hydrolysis. In a prescriptive sense this cleavage can be used to recover peptides that have undergone tryptophan crosslinking, although the yields drop with increasing peptide length due to competitive cleavage of the amide bonds. The best conditions for cleavage involve heating the dimeric peptides in dilute ethanolic HCl at 150°C in the presence of ten equivalents of ethanedithiol. Copyright (C) 1998 Elsevier Science Ltd.
USE OF ESTER DERIVATIVE OF TRYPTOPHAN AS DEODORANT AND/OR PERFUME AGENT
-
, (2016/07/05)
This invention relates to the use of at least one following compound having formula (I), as well as the salts thereof, the optical and geometric isomers thereof, and the solvates thereof, as deodorant agent for treating body odor, preferably underarm odor:
Resolution of N-protected amino acid esters using whole cells of Candida parapsilosis ATCC 7330
Stella, Selvaraj,Chadha, Anju
experimental part, p. 457 - 460 (2010/06/21)
Whole cells of Candida parapsilosis ATCC 7330 were used for the resolution of N-acetyl amino acid esters. Excellent enantioselectivities (E = 40 to >500) were achieved for the resolution of N-protected protein and non-protein amino acid esters giving good yields (28-50%) and high enantiomeric excesses (up to >99%) for both enantiomers.