35788-31-9 Usage
Description
(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-N-[2-(dimethylamino)ethyl]-3,4-dihydroxytetrahydrofuran-2-carboxamide (non-preferred name) is a nucleoside analog with a complex structure, featuring a purine base and a tetrahydrofuran-2-carboxamide backbone. It has a molecular formula of C15H22N6O4 and a molecular weight of 354.37 g/mol. (2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-N-[2-(dimethylamino)ethyl]-3,4-dihydroxytetrahydrofuran-2-carboxamide (non-preferred name) is known for its potential interactions with various enzymes and biological processes, making it a valuable component in pharmaceuticals, biochemistry, and molecular biology research.
Uses
Used in Pharmaceutical Research:
(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-N-[2-(dimethylamino)ethyl]-3,4-dihydroxytetrahydrofuran-2-carboxamide (non-preferred name) is used as a pharmaceutical research compound for its ability to interact with various enzymes and biological processes. Its unique structure allows it to be a potential candidate for the development of new drugs and therapies.
Used in Biochemistry and Molecular Biology Research:
In the fields of biochemistry and molecular biology, (2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-N-[2-(dimethylamino)ethyl]-3,4-dihydroxytetrahydrofuran-2-carboxamide (non-preferred name) serves as an important research tool. Its interactions with enzymes and other biological molecules can provide valuable insights into the mechanisms of various cellular processes, contributing to a better understanding of biological systems and the development of targeted therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 35788-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,7,8 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 35788-31:
(7*3)+(6*5)+(5*7)+(4*8)+(3*8)+(2*3)+(1*1)=149
149 % 10 = 9
So 35788-31-9 is a valid CAS Registry Number.
35788-31-9Relevant articles and documents
Modification of the 5' Position of Purine Nucleosides. 2. Synthesis and Some Cardiovascular Properties of Adenosine-5'-(N-substituted)carboxamides
Prasad, Raj Nandan,Bariana, Dilbagh S.,Fung, Anthony,Savic, Milica,Tietje, Karin,et al.
, p. 313 - 319 (2007/10/02)
We have shown previously that the esters of adenosine-5'-carboxylic acid (10) represent a new class of potent nontoxic coronary vasodilators.For example, the ethyl ester (12), which is active by an intraduodenal or intravenous route in dogs, causes a larg
