19149-48-5 Usage
Pentofuranose sugar molecule
A five-carbon sugar structure derived from a pentose sugar, which is a key component in the formation of nucleic acids.
Tetrahydropyrimidin-2(1H)-one ring structure
A four-membered nitrogen-containing ring structure with one additional carbon atom, which is fused to the pentofuranose sugar molecule.
Nucleoside analog
A compound with a similar structure to nucleosides found in DNA and RNA, which can interact with biological systems and potentially be used as antiviral or anticancer agents.
Pharmaceutical applications
The potential use of 1-pentofuranosyltetrahydropyrimidin-2(1H)-one in the development of drugs for the treatment of viral infections and cancer.
Medicinal chemistry
The field of study focused on the design, synthesis, and development of new drugs, in which 1-pentofuranosyltetrahydropyrimidin-2(1H)-one is an important target for further research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 19149-48-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,1,4 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19149-48:
(7*1)+(6*9)+(5*1)+(4*4)+(3*9)+(2*4)+(1*8)=125
125 % 10 = 5
So 19149-48-5 is a valid CAS Registry Number.
19149-48-5Relevant articles and documents
Organic compounds and process
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, (2008/06/13)
Novel hydrogenated pyrimidine nucleosides and nucleotides are produced by catalytic hydrogenation, particularly in the presence of a rhodium catalyst. The novel compounds are specifically used to inhibit deaminating enzymes, which would inactivate cytosine arabinoside by conversion to uridine arabinoside. Cytosine arabinoside is used for its anti-viral, particularly anti-herpes and anticytotoxic activity in mammals and birds, as well as to destroy phages which interfere with the production of antibiotics. Novel formulations containing cytosine arabinoside and the hydrogenated pyrimidine nucleosides are advantageous to provide prolonged cytosine arabinoside effects.
