98092-14-9 Usage
Uses
Used in Pharmaceutical Research:
ISOVALERYL-PHE-NLE-STA-ALA-STA-OH is used as a research compound for investigating its potential therapeutic effects and mechanisms of action in various medical conditions and diseases. Its unique structure and composition allow researchers to explore its interactions with biological systems and its potential as a drug candidate.
Used in Drug Development:
This synthetic peptide is used as a starting point for the development of new drugs and therapeutic agents. Its ability to modify and influence physiological processes and biological systems within the body makes it a valuable tool for designing and optimizing drug candidates with specific therapeutic targets and mechanisms of action.
Used in Peptide Chemistry:
ISOVALERYL-PHE-NLE-STA-ALA-STA-OH is used as a model compound in peptide chemistry to study the synthesis, structure, and properties of peptides. Its unique composition allows researchers to investigate the effects of different amino acids and modifications on peptide stability, folding, and function, contributing to the understanding of peptide-based drug design and development.
Used in Medical Applications:
ISOVALERYL-PHE-NLE-STA-ALA-STA-OH has potential applications in various medical fields, including the treatment of diseases and conditions that involve the modulation of physiological processes and biological systems. Its potential therapeutic use may be explored in areas such as inflammation, pain management, neurodegenerative disorders, and other conditions that could benefit from the modulation of specific biological pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 98092-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,9 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 98092-14:
(7*9)+(6*8)+(5*0)+(4*9)+(3*2)+(2*1)+(1*4)=159
159 % 10 = 9
So 98092-14-9 is a valid CAS Registry Number.
InChI:InChI=1/C39H65N5O9/c1-9-10-16-29(43-37(51)31(42-34(47)19-25(6)7)20-27-14-12-11-13-15-27)39(53)44(35(48)21-32(45)28(40)17-23(2)3)38(52)26(8)41-30(18-24(4)5)33(46)22-36(49)50/h11-15,23-26,28-33,41,45-46H,9-10,16-22,40H2,1-8H3,(H,42,47)(H,43,51)(H,49,50)/t26-,28-,29-,30?,31-,32-,33-/m0/s1
98092-14-9Relevant academic research and scientific papers
Pepstatin Analogues as Novel Renin Inhibitors
Guegan, Remy,Diaz, Joseph,Cazaubon, Catherine,Beaumont, Michel,Carlet, Claude,et al.
, p. 1152 - 1159 (2007/10/02)
Pepstatin analogues corresponding to the general formula A-X-Y-Sta-Ala-Sta-R were synthesized in solution phase.Various changes in the nature of the A, X, and Y groups were made to improve the inhibitory potency against human plasma renin activity.The res
