109403-64-7 Usage
Description
N-(2-Furanylmethyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine is a purine analog with a unique molecular structure, featuring a furanyl group and a tetrahydro-2H-pyran-2-yl group. It is also known as 2-Furanyl-N-(tetrahydro-2H-pyran-2-yl)adenine and is derived from adenine, a nucleobase present in DNA and RNA. N-(2-Furanylmethyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine may exhibit potential biological activity, particularly in anti-inflammatory or anti-cancer properties, due to its distinct molecular interactions with biological molecules.
Uses
Used in Pharmaceutical Industry:
N-(2-Furanylmethyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine is used as a potential therapeutic agent for its possible anti-inflammatory or anti-cancer properties. Its unique molecular structure allows it to interact with biological molecules in a specific manner, which may impact cellular processes or signaling pathways related to inflammation or cancer.
Used in Research Applications:
In the field of scientific research, N-(2-Furanylmethyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine serves as a valuable compound for studying the effects of purine analogs on biological systems. It can be utilized in experiments to explore its potential interactions with cellular processes, signaling pathways, and its overall impact on health and disease.
Further research is necessary to fully understand the potential uses and effects of N-(2-Furanylmethyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine, as its specific applications and mechanisms of action are not yet completely known.
Check Digit Verification of cas no
The CAS Registry Mumber 109403-64-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,4,0 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109403-64:
(8*1)+(7*0)+(6*9)+(5*4)+(4*0)+(3*3)+(2*6)+(1*4)=107
107 % 10 = 7
So 109403-64-7 is a valid CAS Registry Number.
109403-64-7Relevant articles and documents
X-ray structure, NMR and stability-in-solution study of 6-(furfurylamino)-9-(tetrahydropyran-2-yl)purine - A new active compound for cosmetology
Walla, Jan,Szü?ová, Lucie,Císa?ová, Ivana,Gucky, Tomá?,Zatloukal, Marek,Dole?al, Karel,Greplová, Jarmila,Massino, Frank J.,Strnad, Miroslav
, p. 376 - 380 (2010)
The crystal and molecular structure of 6-(furfurylamino)-9-(tetrahydropyran-2-yl)purine (1) was determined at 150(2) K. The compound crystallizes in monoclinic P21/c space group with a = 10.5642(2), b = 13.6174(3), c = 10.3742(2) ?, V = 1460.78(5) ?3, Z = 4, R(F) = for 3344 unique reflections. The purine moiety and furfuryl ring are planar and the tetrahydropyran-2-yl is disordered in the ratio 1:3, probably due to the chiral carbon atom C(17). The individual 1H and 13C NMR signals were assigned by 2D correlation experiments such as 1H-1H COSY and ge-2D HSQC. Stability-in-solution was determined in methanol/water in acidic pH (3-7).
6,8-DISUBSTITUTED-9-(HETEROCYCLYL)PURINES, COMPOSITIONS CONTAINING THESE DERIVATIVES AND THEIR USE IN COSMETIC AND MEDICINAL APPLICATIONS
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Page/Page column 18, (2016/07/05)
6,8-Disubstituted-9-(heterocyclyl) purines which can be used in pharmaceutical and cosmetic compositions and/or applications are provided. These 6,8-disubstituted-9-(heterocyclyl) purines have a wide range of biological activities, including for example antioxidant, anti-inflammatory, anti-senescent, as well as well as other activities which are especially useful in pharmaceutical and cosmetic applications.
Synthesis of 6-alkyl- and arylamino-9-(tetrahydro-2-pyranyl)purines via 6-methylsulfonylpurine
Villar, Jose Daniel Figueroa,Motta, Marita Almeida
, p. 1005 - 1015 (2007/10/03)
A series of six potential plant hormones, 6-alky- and arylamino-9- (tetrahydro-2-pyranyl)purines were prepared in three steps in 35 to 45% overall yield from 6-methylthiopurine via 6-methylsulfonylpurine.
