59515-83-2 Usage
Uses
Used in Research Applications:
4-AMINO-3,5-DIIODO-L-PHENYLALANINE is used as a research tool for studying protein structure and function. Its unique properties make it valuable for investigating various biological processes and mechanisms.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 4-AMINO-3,5-DIIODO-L-PHENYLALANINE is used as a compound for the development of new drugs and treatments. Its ability to interact with biological systems makes it a promising candidate for creating novel therapeutic agents.
Used in Neurological Disorder Treatment:
4-AMINO-3,5-DIIODO-L-PHENYLALANINE has potential therapeutic applications in the treatment of certain neurological disorders. Its unique chemical structure may offer new avenues for addressing these conditions and improving patient outcomes.
Used in Cancer Treatment:
4-AMINO-3,5-DIIODO-L-PHENYLALANINE also shows promise in the treatment of certain cancers. Its ability to modify biological systems may contribute to the development of new cancer therapies and improve existing treatment options.
Check Digit Verification of cas no
The CAS Registry Mumber 59515-83-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,5,1 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59515-83:
(7*5)+(6*9)+(5*5)+(4*1)+(3*5)+(2*8)+(1*3)=152
152 % 10 = 2
So 59515-83-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H10I2N2O2/c10-5-1-4(2-6(11)8(5)13)3-7(12)9(14)15/h1-2,7H,3,12-13H2,(H,14,15)
59515-83-2Relevant academic research and scientific papers
Photoaffinity labeling of the angiotensin II receptor. 1. Synthesis and biological activities of the labeling peptides.
Escher et al.
, p. 860,862 (2007/10/06)
The synthesis and biological activities of analogues of the peptide hormone angiotensin II (AT) for use in photoaffinity labeling and receptor isolation are described. In the modified sequence of AT, Sar-Arg-Val-Tyr-Val-His-Pro-Phe, the aromatic residues
