120225-53-8 Usage
General Description
The chemical (2S,3S,4R,5R)-5-[6-amino-2-(phenethylamino)purin-9-yl]-N-ethyl-3,4-dihydroxy-oxolane-2-carboxamide is a compound with a complex structure containing a purine base, an amino group, an ethyl group, and a carboxamide functional group. The molecule has a three-dimensional arrangement of atoms, with specific geometries at the chiral centers denoted by the S and R configurations. The compound is an N-ethyl derivative of an oxolane-2-carboxamide containing a purine base, which is often found in nucleic acids like DNA and RNA. The presence of amino and hydroxy groups suggests potential involvement in biological processes or pharmaceutical applications. Its precise role or function in biological systems would depend on its specific interactions with other molecules and cellular processes.
Check Digit Verification of cas no
The CAS Registry Mumber 120225-53-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,2,2 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 120225-53:
(8*1)+(7*2)+(6*0)+(5*2)+(4*2)+(3*5)+(2*5)+(1*3)=68
68 % 10 = 8
So 120225-53-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H25N7O4/c1-2-22-18(30)15-13(28)14(29)19(31-15)27-10-24-12-16(21)25-20(26-17(12)27)23-9-8-11-6-4-3-5-7-11/h3-7,10,13-15,19,28-29H,2,8-9H2,1H3,(H,22,30)(H3,21,23,25,26)/t13-,14+,15-,19+/m0/s1
120225-53-8Relevant articles and documents
Synthesis and pharmacological evaluation of dual acting antioxidant a 2A adenosine receptor agonists
Hausler, Nicholas E.,Devine, Shane M.,McRobb, Fiona M.,Warfe, Lyndon,Pouton, Colin W.,Haynes, John M.,Bottle, Steven E.,White, Paul J.,Scammells, Peter J.
, p. 3521 - 3534 (2012/06/04)
A series of adenosine-5′-N-alkylcarboxamides and N 6-(2,2-diphenylethyl)adenosine-5′-N-alkylcarboxamides bearing antioxidant moieties in the 2-position were synthesized from the versatile intermediate, O6-(benzotriazol-1-yl)-2-fluoro
2-(Arylalkylamino)adenosin-5'-uronamides: A New Class of Highly Selective Adenosine A2 Receptor Ligands
Hutchison, Alan J.,Williams, Michael,Jesus, Reynalda, de,Yokoyama, Rina,Oei, Howard H.,et al.
, p. 1919 - 1924 (2007/10/02)
The synthesis and receptor-binding profiles at adenosine receptor subtypes for a series of 2-(arylalkylamino)adenosin-5'-uronamides is described.Halogenated 2-phenethylamino analogues such as 3e show greater than 200-fold selectivity for the A2 receptor s
