81408-49-3 Usage
Uses
Used in Pharmaceutical Industry:
rac erythro-9-(2-Hydroxy-3-nonyl)adenine, Hydrochloride is used as a selective inhibitor for cGMP-stimulated phosphodiesterase (PDE2) for its ability to modulate intracellular cGMP levels, which can have therapeutic effects in treating certain diseases.
Used in Enzyme Inhibition:
In the field of biochemistry, rac erythro-9-(2-Hydroxy-3-nonyl)adenine, Hydrochloride is used as a potent inhibitor of adenosine deaminase, an enzyme involved in the breakdown of adenosine. This inhibition can be useful in studying enzyme function and developing treatments for related conditions.
Used in Research Applications:
As a chemical compound with specific inhibitory properties, rac erythro-9-(2-Hydroxy-3-nonyl)adenine, Hydrochloride is used in research settings to investigate the roles of PDE2 and adenosine deaminase in various biological processes and disease mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 81408-49-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,0 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81408-49:
(7*8)+(6*1)+(5*4)+(4*0)+(3*8)+(2*4)+(1*9)=123
123 % 10 = 3
So 81408-49-3 is a valid CAS Registry Number.
81408-49-3Relevant academic research and scientific papers
Enantiospecific synthesis of some bioactive amino alcohols and related compounds from cyclohexylideneglyceraldehyde
Sharma, Anubha,Chattopadhyay, Subrata
, p. 883 - 890 (2011/07/06)
Two bioactive amino alcohols or related derivatives, 2-aminohexadecanol I and erythro-9-(2-hydroxy-3-nonyl)adenine hydrochloride (EHNA hydrochloride) IIa, have been synthesized from some enantiomerically pure 3-alkylglycerols. The required C-3 epimeric 3-
Synthesis of Inhibitors of Adenosine Deaminase. A Total Synthesis of erythro-3-(Adenin-9-yl)-2-nonanol and Its Isomers from Chiral Precursors
Baker, David C.,Hawkins, L. D.
, p. 2179 - 2184 (2007/10/02)
The synthesis of both isomers of EHNA2 ("erythrohydroxynonyladenine") from D- and L-rhamnose is described.The key intermediates, (R)- and (S)-2-(benzyloxy)propanal, derived respectively from 5-O-benzyl-D- and -L-rhamnitol, were each condensed w