30802-26-7 Usage
Uses
Used in Drug Design and Chemical Biology:
AC-ALA-ALA-OME is used as a building block for the synthesis of peptides and peptidomimetics, contributing to the development of new pharmaceutical agents. Its incorporation into these molecules can enhance their stability, bioavailability, and target specificity.
Used in Therapeutic Applications:
AC-ALA-ALA-OME is used as a potential therapeutic agent for targeting specific receptors or enzymes in the body, which may have implications for the treatment of various diseases and conditions.
Used in Research and Development:
AC-ALA-ALA-OME is used as a research tool for studying protein-protein interactions, aiding in the understanding of complex biological processes and the discovery of new drug targets.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, AC-ALA-ALA-OME is used as a component in the development of new drug candidates with improved pharmacokinetic properties, potentially leading to more effective and safer medications.
Check Digit Verification of cas no
The CAS Registry Mumber 30802-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,0 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30802-26:
(7*3)+(6*0)+(5*8)+(4*0)+(3*2)+(2*2)+(1*6)=77
77 % 10 = 7
So 30802-26-7 is a valid CAS Registry Number.
30802-26-7Relevant academic research and scientific papers
COMPOUNDS FOR AMIDE-FORMING REACTIONS
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Page/Page column 11; 18, (2014/01/07)
Provided herein is a compound of Formula I, that displays remarkable physicochemical properties as a peptide-coupling additive for peptide-forming reactions in water, wherein said coupling reactions proceed without measurable racemization. A method of pro
A new oxyma derivative for nonracemizable amide-forming reactions in water
Wang, Qinghui,Wang, Yong,Kurosu, Michio
supporting information; experimental part, p. 3372 - 3375 (2012/09/07)
An Oxyma derivative, (2,2-dimethyl-1,3-dioxolan-4-yl)methyl 2-cyano-2-(hydroxyimino)acetate (2), displayed remarkable physicochemical properties as a peptide-coupling additive for peptide-forming reactions in water. Short peptides to oligopeptides could b
Thermitase - A Thermostable Serine Protease. I. Synthesis of Alanine Peptide Esters as Substrates of the Enzyme
Jahreis, Guenther,Fittkau, Siegfried
, p. 35 - 40 (2007/10/02)
The synthesis of N-acetylated and N-succinylated peptide esters of alanine is described.The peptides are built up from the Z-protected peptides by liquid phase fragment condensation and by acylation of the deprotected peptide esters.The kinetic parameters Km and kcat of some compounds are presented.
