93629-01-7 Usage
Uses
Used in Pharmaceutical Development:
(N-tert-butyloxycarbonyl-cysteinyl-alanyl-cysteinyl-methylamide)2 is used as a research compound for pharmaceutical development due to its peptide nature and potential for studying protein-protein interactions. Its structure allows for the investigation of various biological processes and the design of new drugs targeting specific interactions.
Used in Biotechnology:
In the biotechnology industry, (N-tert-butyloxycarbonyl-cysteinyl-alanyl-cysteinyl-methylamide)2 is used as a key component in the development of novel bioactive molecules. Its unique structure and properties make it an attractive candidate for creating new compounds with potential applications in various therapeutic areas.
Used in Drug Design:
(N-tert-butyloxycarbonyl-cysteinyl-alanyl-cysteinyl-methylamide)2 is utilized as a building block in drug design, particularly for the development of peptide-based therapeutics. The presence of the N-tert-butyloxycarbonyl group provides a protective mechanism for the cysteine residues, allowing for the creation of peptides with specific properties and functions.
Used in Protein-Protein Interaction Studies:
(N-tert-butyloxycarbonyl-cysteinyl-alanyl-cysteinyl-methylamide)2 is employed as a tool in the study of protein-protein interactions. Its structure and properties facilitate the investigation of how proteins interact with each other, which is crucial for understanding various biological processes and developing targeted therapies.
Overall, (N-tert-butyloxycarbonyl-cysteinyl-alanyl-cysteinyl-methylamide)2 is a versatile and important chemical with a wide range of applications in biotechnology, pharmaceutical development, and drug design, making it a valuable asset in the ongoing quest to advance medical research and treatment options.
Check Digit Verification of cas no
The CAS Registry Mumber 93629-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,2 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 93629-01:
(7*9)+(6*3)+(5*6)+(4*2)+(3*9)+(2*0)+(1*1)=147
147 % 10 = 7
So 93629-01-7 is a valid CAS Registry Number.
InChI:InChI=1/C30H52N8O10S4/c1-15(33-25(43)19(13-51)35-27(45)47-29(3,4)5)21(39)37-23(41)17(11-49)31-9-10-32-18(12-50)24(42)38-22(40)16(2)34-26(44)20(14-52)36-28(46)48-30(6,7)8/h9-10,15-20,31-32,49-52H,11-14H2,1-8H3,(H,33,43)(H,34,44)(H,35,45)(H,36,46)(H,37,39,41)(H,38,40,42)/b10-9+/t15-,16-,17-,18-,19-,20-/m0/s1
93629-01-7Relevant academic research and scientific papers
Kishore, R.,Balaram, P.
, p. 778 - 779 (1984)
The cyclic biscystine peptides (1a) and (1b) adopt antiparallel β-sheet conformations in solution, characterized by distinctive 1H n.m.r. spectral parameters.
Cystine Peptides. The Antiparallel β-Sheet Conformation of Two Synthetic Cyclic Bis(cystine peptides)
Kishore, R.,Kumar, A.,Balaram, P.
, p. 8019 - 8023 (2007/10/02)
Conformational studies on the two synthetic cyclic bis(cystine peptides) have been carried out.The NMR data support a C2-symmetric structure possessing four intramolecular hydrogen bonds in CDCl3 and (CD3)2SO solutions.The involvement of the X-NH and NHMe
