63023-95-0 Usage
Uses
Used in Pharmaceutical Applications:
Z-TYR-PHE-OH is used as a pharmaceutical compound for its potential role in modifying biological activity and interactions with other molecules. The presence of the hydroxyl group may enhance its therapeutic properties and contribute to the development of new drugs.
Used in Research Applications:
Z-TYR-PHE-OH is used as a research compound for studying the effects of amino acid modifications on biological activity and interactions. Its unique structure allows scientists to investigate the role of Z-tyrosine and phenylalanine in various biological processes and their potential applications in medicine.
Used in Peptide Synthesis:
Z-TYR-PHE-OH is used as a building block in peptide synthesis, where it can be incorporated into larger peptide structures. This allows for the creation of novel peptides with specific functions and properties, which can be used in various applications, such as drug development and medical research.
Used in Neurotransmitter and Hormone Production:
Z-TYR-PHE-OH is used as a precursor in the production of neurotransmitters and hormones, given its composition of Z-tyrosine and phenylalanine. These molecules play crucial roles in the nervous system and endocrine system, respectively, and are essential for maintaining proper physiological function.
Check Digit Verification of cas no
The CAS Registry Mumber 63023-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,0,2 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63023-95:
(7*6)+(6*3)+(5*0)+(4*2)+(3*3)+(2*9)+(1*5)=100
100 % 10 = 0
So 63023-95-0 is a valid CAS Registry Number.
InChI:InChI=1/C26H26N2O6/c29-21-13-11-19(12-14-21)15-22(28-26(33)34-17-20-9-5-2-6-10-20)24(30)27-23(25(31)32)16-18-7-3-1-4-8-18/h1-14,22-23,29H,15-17H2,(H,27,30)(H,28,33)(H,31,32)
63023-95-0Relevant articles and documents
N-(Cbz- and Fmoc-α-aminoacyl)benzotriazoles: Stable derivatives enabling peptide coupling of Tyr, Trp, Cys, Met, and Gln with free amino acids in aqueous media with complete retention of chirality
Katritzky, Alan R.,Angrish, Parul,Huer, Deniz,Suzuki, Kazuyuki
, p. 397 - 402 (2007/10/03)
Crystalline, chirally stable N-(Cbz- and Fmoc-α-aminoacyl) benzotriazoles 2a-f, activated derivatives of Tyr, Trp, Cys, Met and Gln undergo peptide coupling in aqueous media with unprotected L-Ala-OH and L-Phe-OH to give the chiral dipeptides in 70-98% yi
