16869-42-4 Usage
Uses
Used in Research Applications:
H-GAMMA-GLU-ABU-OH is used as a research compound for studying its potential functions and interactions in biological systems. H-GAMMA-GLU-ABU-OH's unique structure and amino acid composition make it a valuable subject for scientific inquiry.
Used in Pharmaceutical Applications:
H-GAMMA-GLU-ABU-OH is used as a potential therapeutic agent in the development of new drugs. Its peptide nature suggests that it may have applications in treating various diseases or conditions, although further research is required to determine its efficacy and safety.
Used in Biotechnological Applications:
H-GAMMA-GLU-ABU-OH is used as a component in biotechnological processes, such as the production of enzymes or other bioactive molecules. Its peptide structure may offer advantages in these applications, but more investigation is needed to explore its potential fully.
Check Digit Verification of cas no
The CAS Registry Mumber 16869-42-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,6 and 9 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16869-42:
(7*1)+(6*6)+(5*8)+(4*6)+(3*9)+(2*4)+(1*2)=144
144 % 10 = 4
So 16869-42-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H16N2O5/c1-2-5(8(13)14)11-6(9(15)16)3-4-7(10)12/h5-6,11H,2-4H2,1H3,(H2,10,12)(H,13,14)(H,15,16)/t5-,6-/m0/s1
16869-42-4Relevant articles and documents
Synthesis of γ-Glutamylpeptides by γ-Glutamylcysteine Synthetase from Proteus mirabilis
Nakayama, Reiko,Kumagai, Hedehiko,Maruyama, Takashi,Tochikura, Tatsurokuro,Ueno, Tamio,Fukami, Hiroshi
, p. 2839 - 2846 (2007/10/02)
Syntheses of various γ-glutamylpeptides were examined taking use of the highly purified γ-glutamylcysteine synthetase from Proteus mirabilis.The accumulation of each peptide was measured after long time incubation, and good formation was observed in the synthesis of peptides of following amino acids, L-cysteine, L-α-aminobutyrate, L-serine, L-homoserine, glycine, L-alanine, L-norvaline, L-lysine, L-threonine, taurine and L-valine.Peptide syntheses were confirmed by analyses of the component amino acids, after hydrolysis of the peptides.The structure of the glutamylpeptides, especially the peptide-linkage at the γ-carbonyl residue of L-glutamate, was determined by mass spectrometry of the N-trifluoroacetyl methylester derivatives of the glutamylpeptides.Enzymatic synthesis of γ-glutamyl-L-α-aminobutyrate was also confirmed by PMR spectrometry in the comparison with chemically synthesized compound.
