CAS 3001-45-4
:6-amino-9-pentofuranosyl-7,9-dihydro-8H-purine-8-thione
Description:
6-Amino-9-pentofuranosyl-7,9-dihydro-8H-purine-8-thione, with the CAS number 3001-45-4, is a purine derivative that exhibits characteristics typical of nucleobases and nucleosides. This compound features a purine ring structure, which is essential in the formation of nucleic acids, and includes an amino group at the 6-position and a thione group at the 8-position, contributing to its reactivity and biological activity. The presence of the pentofuranosyl moiety indicates that it is a nucleoside, which plays a crucial role in cellular metabolism and genetic information transfer. Its structural features suggest potential interactions with biological macromolecules, making it of interest in biochemical and pharmaceutical research. The compound may exhibit solubility in polar solvents, and its stability can be influenced by pH and temperature. Overall, this substance is significant in the study of nucleoside analogs and their applications in medicinal chemistry, particularly in the development of antiviral and anticancer agents.
Formula:C10H13N5O4S
InChI:InChI=1/C10H13N5O4S/c11-7-4-8(13-2-12-7)15(10(20)14-4)9-6(18)5(17)3(1-16)19-9/h2-3,5-6,9,16-18H,1H2,(H,14,20)(H2,11,12,13)
Synonyms:- 6-Amino-9-pentofuranosyl-9H-purine-8-thiol
- 9H-purine-8-thiol, 6-amino-9-pentofuranosyl-
- 8-Mercaptoadenosine
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Found 3 products.
Adenosine,7,8-dihydro-8-thioxo-
CAS:Formula:C10H13N5O4SPurity:97%Color and Shape:SolidMolecular weight:299.30636-Amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-7H-purine-8(9H)-thione
CAS:<p>6-Amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-7H-purine-8(9H)-thione</p>Purity:97%Molecular weight:299.31g/mol7,8-Dihydro-8-thioxo-adenosine
CAS:<p>7,8-Dihydro-8-thioxo-adenosine is a synthetic nucleoside that activates the synthesis of DNA and RNA by acting as a ribonucleotide. It also has antiviral and anticancer activities. 7,8-Dihydro-8-thioxo-adenosine is an antiviral agent against herpesviruses and retroviruses. The antitumor activity of this compound is due to its ability to inhibit the proliferation of tumor cells by inhibiting DNA synthesis. 7,8-Dihydro-8-thioxo-adenosine can be used in the treatment of leukemia and other cancers that are sensitive to cytotoxic drugs. This drug has been shown to have low toxicity in rats.</p>Formula:C10H13SN5O4Purity:Min. 95%Molecular weight:299.31 g/mol



