103340-16-5 Usage
Uses
Used in Peptide Synthesis:
BOC-PHE-GLY-GLY-OH is used as a protected amino acid in peptide synthesis for the controlled introduction of specific amino acid residues. The protective BOC group ensures that the amine group remains unreactive during the synthesis process, allowing for the precise assembly of peptide sequences.
Used in Pharmaceutical Development:
In the pharmaceutical industry, BOC-PHE-GLY-GLY-OH is utilized in the development of peptide-based drugs. Its controlled release of the phenylalanine residue upon removal of the BOC group allows for the creation of specific peptide therapeutics with targeted biological activities.
Used in Biochemical Research:
BOC-PHE-GLY-GLY-OH serves as an essential component in biochemical research, where it is employed to study the structure, function, and interactions of peptides. Its controlled release of the phenylalanine residue provides researchers with a tool to investigate the role of specific amino acids in peptide function and stability.
Used in the Creation of Complex Peptides:
BOC-PHE-GLY-GLY-OH is a crucial building block in the synthesis of complex peptides for various scientific and medical applications. Its versatility in peptide synthesis allows for the development of peptides with specific properties, such as enhanced stability, bioavailability, or targeted biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 103340-16-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,3,4 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 103340-16:
(8*1)+(7*0)+(6*3)+(5*3)+(4*4)+(3*0)+(2*1)+(1*6)=65
65 % 10 = 5
So 103340-16-5 is a valid CAS Registry Number.
InChI:InChI=1/C18H25N3O6/c1-18(2,3)27-17(26)21-13(9-12-7-5-4-6-8-12)16(25)20-10-14(22)19-11-15(23)24/h4-8,13H,9-11H2,1-3H3,(H,19,22)(H,20,25)(H,21,26)(H,23,24)
103340-16-5Relevant academic research and scientific papers
Novel peptide
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, (2008/06/13)
Peptides represented by the formula: STR1 wherein: X represents Met, Met(O), Nle, or Ile; Y represents a cystine residue or an α-amino suberic acid residue; Z represents Gly or Ala; m, n, and p each represent 0 or 1; A represents Ser, Ser-Ser, Arg-Ser-Ser, Arg-Arg-Ser-Ser, Leu-Arg-Arg-Ser-Ser, or Ser-Leu-Arg-Arg-Ser-Ser; and B represents Asn, Asn-Ser, Asn-Ser-Phe, Asn-Ser-Phe-Arg, or Asn-Ser-Phe-Arg-Tyr; with the proviso that α-hANP(1-28), α-rANP(1-28), α-rANP(4-28), α-rANP(5-27), α-rANP(5-25), and α-rANP(3-28) are excluded from the compounds represented by the formula are disclosed along with methods of using these compounds.
