35788-28-4 Usage
Uses
Used in Biochemical Research:
(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxy-N-(2-hydroxyethyl)tetrahydrofuran-2-carboxamide (non-preferred name) is used as a research compound for studying its potential involvement in biochemical processes such as protein binding or enzyme inhibition. Its unique functional groups and complex structure make it a promising candidate for investigating its interactions with biological systems and understanding its role in various biological pathways.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxy-N-(2-hydroxyethyl)tetrahydrofuran-2-carboxamide (non-preferred name) may be used as a starting point for the development of new drugs targeting specific diseases. Its potential involvement in biochemical processes and interactions with biological systems make it a valuable compound for designing and optimizing therapeutic agents with novel mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 35788-28-4 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, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35788-28:
(7*3)+(6*5)+(5*7)+(4*8)+(3*8)+(2*2)+(1*8)=154
154 % 10 = 4
So 35788-28-4 is a valid CAS Registry Number.
35788-28-4Relevant academic research and scientific papers
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
Adenosine-5'-carboxylic acid amides
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, (2008/06/13)
Adenosine-5'-carboxylic acid amides represented by the formula STR1 wherein R1 and R2 are each selected from the group consisting of hydrogen, loweralkyl, lowerhaloalkyl, lowerhydroxyalkyl, lowercycloalkyl, loweralkylcycloalkyl, loweralkenyl, lowerhaloalkenyl, lowerhydroxyalkenyl, loweralkynyl, lowerhaloalkynyl, benzylamino, phenyl, loweralkylphenyl, loweralkoxyloweralkyl, substituted phenyl, 2-methylfuran or di(C1 -C4)alkylamino(C1 -C4)alkyl, adamantyl or R1 and R2 taken together form a 5 or 6 membered heterocyclic moiety; R3 and R4 are hydrogen or acyl, or taken together form an isopropylidene or a benzylidene group; or a pharmaceutically acceptable acid addition salt thereof.
