58048-25-2 Usage
Description
(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-N-(cyclopropylmethyl)-3,4-dihydroxytetrahydrofuran-2-carboxamide (non-preferred name) is a complex organic compound that features a cyclopropylmethyl group, a tetrahydrofuran ring, and an amino-purinyl group. It is a dihydroxy carboxamide and bears structural resemblance to nucleoside analogs, which are commonly found in antiviral and anticancer medications. (2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-N-(cyclopropylmethyl)-3,4-dihydroxytetrahydrofuran-2-carboxamide (non-preferred name) holds potential for medicinal applications due to its similarity to bioactive molecules, although further research and testing are necessary to ascertain its specific uses and effects.
Uses
Used in Pharmaceutical Industry:
(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-N-(cyclopropylmethyl)-3,4-dihydroxytetrahydrofuran-2-carboxamide (non-preferred name) is used as a potential candidate for the development of new antiviral and anticancer drugs due to its structural similarity to nucleoside analogs, which are known for their therapeutic effects in these areas.
Used in Research and Development:
In the field of medicinal chemistry, this compound serves as a subject for research and development to explore its potential as a lead compound for the creation of novel therapeutic agents. Its unique structure may offer new avenues for targeting viral and cancerous processes, pending further investigation into its pharmacological properties and mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 58048-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,4 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 58048-25:
(7*5)+(6*8)+(5*0)+(4*4)+(3*8)+(2*2)+(1*5)=132
132 % 10 = 2
So 58048-25-2 is a valid CAS Registry Number.
58048-25-2Relevant 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