75539-79-6 Usage
Uses
Used in Pharmaceutical Industry:
N-CBZ-D-PHE-PHE-GLY is used as a building block in peptide synthesis for the development of new pharmaceuticals. Its role in creating longer peptide chains allows for the design and synthesis of various therapeutic agents with specific functions and properties.
Used in Research:
N-CBZ-D-PHE-PHE-GLY is used as a research tool for studying the interactions of peptides with opioid receptors in the body. This helps scientists understand the mechanisms of action and potential therapeutic applications of peptide-based drugs.
Used in Opioid Antagonist Development:
N-CBZ-D-PHE-PHE-GLY has been studied for its potential as an opioid antagonist. Its structure and interactions with opioid receptors make it a promising candidate for the development of new treatments for opioid addiction and related disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 75539-79-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,5,3 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 75539-79:
(7*7)+(6*5)+(5*5)+(4*3)+(3*9)+(2*7)+(1*9)=166
166 % 10 = 6
So 75539-79-6 is a valid CAS Registry Number.
InChI:InChI=1/C28H29N3O6/c32-25(33)18-29-26(34)23(16-20-10-4-1-5-11-20)30-27(35)24(17-21-12-6-2-7-13-21)31-28(36)37-19-22-14-8-3-9-15-22/h1-15,23-24H,16-19H2,(H,29,34)(H,30,35)(H,31,36)(H,32,33)/t23-,24+/m0/s1
75539-79-6Relevant academic research and scientific papers
Juby, Carl D.,Richardson, Christopher D.,Brousseau, Roland
, p. 879 - 882 (1991)
The solid phase synthesis of 3′ deoxyoligonucleotide (17 mer)-peptide conjugates is described. The oligonucleotide is complementary to the template strand of the measles virus in the region of the nucleocapsid protein on the 60 nucleotide leader RNA. The conjugates were synthesized on teflon support using a combination of solid phase FMOC peptide chemistry and phosphoramidite chemistry linked by a branched modifier.
Peptidophospholipids: Synthesis, phospholipase A2 catalyzed hydrolysis, and application to development of phospholipid prodrugs
Rosseto, Renato,Hajdu, Joseph
, p. 110 - 116 (2014/07/08)
New phospholipid analogues incorporating sn-2-peptide substituents have been prepared to probe the fundamental structural requirements for phospholipase A2 catalyzed hydrolysis of PLA2-directed synthetic substrates. Two structurally
