16422-07-4 Usage
Description
H-ALA-ALA-GLY-OH is a chemical compound composed of three amino acids alanine, glycine, and alanine linked in a linear sequence. It is widely used in biochemistry and pharmaceutical research as a model compound for studying peptide formation, stability, and interactions. H-ALA-ALA-GLY-OH also serves as a building block for creating larger peptides and proteins, as well as for drug development. Due to its ability to mimic certain structural and functional properties of naturally occurring peptides and proteins, H-ALA-ALA-GLY-OH has potential applications in medicine and biotechnology. It is a valuable tool for understanding and manipulating the properties of peptides and proteins in various scientific and industrial contexts.
Uses
Used in Biochemistry and Pharmaceutical Research:
H-ALA-ALA-GLY-OH is used as a model compound for studying peptide formation, stability, and interactions. It helps researchers understand the fundamental properties of peptides and proteins, which is crucial for developing new drugs and therapies.
Used in Peptide and Protein Synthesis:
H-ALA-ALA-GLY-OH is used as a building block for creating larger peptides and proteins. Its linear sequence of amino acids allows for the development of complex structures with specific functions, which can be applied in various scientific and industrial applications.
Used in Drug Development:
H-ALA-ALA-GLY-OH is used in drug development as a potential therapeutic agent or as a component of drug delivery systems. Its ability to mimic naturally occurring peptides and proteins makes it a promising candidate for the development of new drugs with specific targets and mechanisms of action.
Used in Medicine:
H-ALA-ALA-GLY-OH has potential applications in medicine due to its ability to mimic certain structural and functional properties of naturally occurring peptides and proteins. It can be used for the development of new therapeutic agents or as a component of diagnostic tools.
Used in Biotechnology:
H-ALA-ALA-GLY-OH is used in biotechnology for the development of novel biomaterials, biosensors, and other applications that require the manipulation of peptide and protein properties. Its versatility and ability to mimic natural peptides and proteins make it a valuable tool in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 16422-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,4,2 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16422-07:
(7*1)+(6*6)+(5*4)+(4*2)+(3*2)+(2*0)+(1*7)=84
84 % 10 = 4
So 16422-07-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H15N3O4/c1-4(9)7(14)11-5(2)8(15)10-3-6(12)13/h4-5H,3,9H2,1-2H3,(H,10,15)(H,11,14)(H,12,13)
