16014-63-4 Usage
Uses
Used in Research and Laboratory Settings:
2-amino-2-carbamimidoyl-acetamide is utilized as a reagent for the synthesis of a variety of organic compounds, contributing to the advancement of chemical research and the development of new materials and pharmaceuticals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-amino-2-carbamimidoyl-acetamide is studied for its potential pharmacological properties, indicating its possible use in the creation of new drugs and therapeutic agents.
Used in Pharmaceutical Development:
Although further research is required, 2-amino-2-carbamimidoyl-acetamide has been investigated for its potential application in the treatment of certain medical conditions, highlighting its prospect as a candidate for future pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 16014-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,1 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16014-63:
(7*1)+(6*6)+(5*0)+(4*1)+(3*4)+(2*6)+(1*3)=74
74 % 10 = 4
So 16014-63-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H8N4O/c4-1(2(5)6)3(7)8/h1H,4H2,(H3,5,6)(H2,7,8)
16014-63-4Relevant academic research and scientific papers
Xanthine oxidase (XO): Relative configuration of complexes formed by the enzyme, 2- or 8-N-alkylhypoxanthines and 2-N-alkyl-8-azahypoxanthines. XII
Biagi,Giorgi,Livi,Scartoni,Tonetti,Lucacchini
, p. 357 - 374 (2007/10/02)
Several 2- or 8-n-alkyl-hypoxanthines and a 2,8-di-n-pentylhypoxanthine were synthesized and tested as substrates or inhibitors of Xanthine Oxidase (XO). 8-Alkyl derivatives showed a substrate behaviour, whereas 2-alkyl substituted compounds were non-substrates and inhibitors. 2,8-di-n-pentylhypoxanthine was ineffective as inhibitor. The comparison between their activity allowed us to conclude that the complexes formed by the enzyme and the cited n-alkylhypoxanthines or 2-n -alkyl-8-azahypoxanthines involve their N(3) and N(9) positions in all the cases. The position of the n-alkyl chain determines the disposition of the molecule inside the complex: 2-n-alkyl-hypoxanthines and 2-n-alkyl-8-azahypoxanthines gave complexes with the same orientation of heterocyclic moieties, opposite that given by 8-n-alkyl-hypoxanthines.
