14535-90-1 Usage
Uses
Used in Pharmaceutical Industry:
Adenosine 5'-pentaphosphate is used as a therapeutic agent for various applications due to its unique properties and interactions with cellular components. It has been found to have potential in treating conditions such as inflammation, cardiovascular diseases, and certain types of cancer.
Used in Research and Development:
In the field of research, adenosine 5'-pentaphosphate is used as a tool to study the mechanisms of cellular signaling and regulation. Its ability to interact with various cellular components makes it a valuable compound for understanding the complex processes within cells.
Used in Drug Delivery Systems:
Similar to gallotannin, adenosine 5'-pentaphosphate can also be incorporated into drug delivery systems to improve its bioavailability and therapeutic outcomes. By using carriers such as organic and metallic nanoparticles, the delivery and efficacy of adenosine 5'-pentaphosphate can be enhanced, making it a more effective treatment option for various conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 14535-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,3 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14535-90:
(7*1)+(6*4)+(5*5)+(4*3)+(3*5)+(2*9)+(1*0)=101
101 % 10 = 1
So 14535-90-1 is a valid CAS Registry Number.
14535-90-1Relevant academic research and scientific papers
Facile and Selective Synthesis of Diadenosine Polyphosphates through Catalysis by Leucyl t-RNA Synthetase Coupled with ATP Regeneration
Nakajima, Hiroshi,Tomioka, Isao,Kitabatake, Senji,Dombou, Munehiko,Tomita, Kosuke
, p. 615 - 624 (2007/10/02)
Leucyl t-RNA synthetase from a thermophilic bacterium, Bacillus stearothermophillus, effectively catalyzed the synthesis of p1,p4-di(adenosine 5'-)tetraphosphate (Ap4A), p1,p5-di(adenosine 5'-)pentaphosphate (Ap5A) and adenosine 5'-tetraphosphate (p4A).In particular, when the reaction was coupled with an ATP recycling system involving thermostable acetate kinase and adenylate kinase, Ap4A and Ap5A were produced selectively in high yields.This reaction is selective, gives high yields and does not require protection of the functional groups of nucleotides, and also it can be carried out in an aqueous solution.This method is superior to the conventional organic synthesis and provides a practical means of the synthesizing diadenosine polyphosphates (ApnA), biologically important compounds.
