1947-42-8 Usage
Uses
Used in Research and Laboratory Settings:
N-α,N-ω-,N-ω′-Tri-Z-D-arginine serves as a valuable tool for studying protein-protein interactions, which is crucial for understanding the molecular mechanisms underlying numerous biological processes.
Used in Drug Development:
N-α,N-ω-,N-ω′-Tri-Z-D-arginine is being explored for its potential in the development of novel drugs and therapies, given its ability to modulate biological processes and its implications in various disease conditions.
Used in Cancer Research and Therapy:
N-α,N-ω-,N-ω′-Tri-Z-D-arginine is studied for its potential therapeutic applications in cancer, where it may contribute to the modulation of processes related to tumor growth, progression, and metastasis.
Used in Cardiovascular Disease Research:
N-α,N-ω-,N-ω′-Tri-Z-D-arginine is also being investigated for its role in cardiovascular disease, potentially offering insights into the mechanisms of heart disease and stroke, and contributing to the development of new treatment strategies.
Used in Neurological Disorders Research:
N-α,N-ω-,N-ω′-Tri-Z-D-arginine is being examined for its potential applications in neurological disorders, where it may help elucidate the molecular pathways involved in conditions such as Alzheimer's, Parkinson's, and multiple sclerosis, and aid in the discovery of new therapeutic approaches.
Check Digit Verification of cas no
The CAS Registry Mumber 1947-42-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,4 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1947-42:
(6*1)+(5*9)+(4*4)+(3*7)+(2*4)+(1*2)=98
98 % 10 = 8
So 1947-42-8 is a valid CAS Registry Number.
1947-42-8Relevant academic research and scientific papers
A practical synthesis of free and protected guanidino acids from amino acids
Lal, Bansi,Gangopadhyay
, p. 2483 - 2486 (2007/10/03)
Synthesis of protected guanidino acids in one pot reaction is achieved. Amino acids are treated with trimethylsilyl chloride, triethylamine, dicarbobenzoxy-S-methyl isothiourea in dichloromethane followed by removal of silyl group by treatment with methanol to give the corresponding carbobenzoxy guanidino acids.
