7093-67-6 Usage
Description
PENTAGLYCINE, also known as a pentapeptide, is a compound comprised of five glycine residues. It is a white powder with unique chemical properties that make it a potential candidate for various applications in the pharmaceutical and medical industries.
Uses
Used in Pharmaceutical Industry:
PENTAGLYCINE is used as a tumor necrosis factor receptor 2 agonist for its potential role in modulating immune responses and treating certain medical conditions. Its specific interaction with the receptor may provide therapeutic benefits in targeted treatments.
Used in Research and Development:
PENTAGLYCINE, due to its unique structure and properties, can be utilized in research and development for understanding the mechanisms of various biological processes and the development of new drugs or therapies. Its role as a pentapeptide may offer insights into peptide-based drug design and synthesis.
Used in Drug Delivery Systems:
Similar to other peptides, PENTAGLYCINE can be employed in drug delivery systems to improve the targeting and efficacy of therapeutic agents. Its small size and specific interactions with receptors may allow for the development of novel drug carriers or targeted drug delivery methods.
Check Digit Verification of cas no
The CAS Registry Mumber 7093-67-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,9 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7093-67:
(6*7)+(5*0)+(4*9)+(3*3)+(2*6)+(1*7)=106
106 % 10 = 6
So 7093-67-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H17N5O6/c11-1-6(16)12-2-7(17)13-3-8(18)14-4-9(19)15-5-10(20)21/h1-5,11H2,(H,12,16)(H,13,17)(H,14,18)(H,15,19)(H,20,21)
7093-67-6Relevant articles and documents
Mechanochemical Prebiotic Peptide Bond Formation**
Cindro, Nikola,Grube?i?, Sa?a,Hernández, José G.,Me?trovi?, Ernest,Stolar, Tomislav,U?arevi?, Krunoslav
supporting information, p. 12727 - 12731 (2021/05/07)
The presence of amino acids on the prebiotic Earth, either stemming from endogenous chemical routes or delivered by meteorites, is consensually accepted. Prebiotically plausible pathways to peptides from inactivated amino acids are still unclear as most oligomerization approaches rely on thermodynamically disfavored reactions in solution. Now, a combination of prebiotically plausible minerals and mechanochemical activation enables the oligomerization of glycine at ambient temperature in the absence of water. Raising the reaction temperature increases the degree of oligomerization concomitantly with the formation of a commonly unwanted cyclic glycine dimer (DKP). However, DKP is a productive intermediate in the mechanochemical oligomerization of glycine. The findings of this research show that mechanochemical peptide bond formation is a dynamic process that provides alternative routes towards oligopeptides and establishes new synthetic approaches for prebiotic chemistry.
PEPTIDE FORMATION FROM AMINO ACID WITH PARTICULATE SEMICONDUCTOR PHOTOCATALYSTS
Onoe, Jun,Kawai, Tomoji,Kawai, Shichio
, p. 1667 - 1670 (2007/10/02)
Peptides of diglycine to pentaglycine are formed from glycine under irradiation in the presence of particulate semiconductor photocatalysts such as TiO2, CdS, CdSe, MoS2, In2O3, and GaP, with and without Pt deposition.Platinization of the semiconductors efficiently enhanced the yield of the peptides.
