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CAS 16975-94-3

:

carbocyclic inosine

Description:
Carbocyclic inosine, identified by the CAS number 16975-94-3, is a modified nucleoside that features a carbocyclic structure, which replaces the typical ribose sugar found in standard nucleosides. This modification enhances its stability and can influence its biological activity. Inosine itself is a purine nucleoside composed of hypoxanthine linked to a ribose sugar, and its carbocyclic variant retains the purine base while altering the sugar component. The characteristics of carbocyclic inosine include its potential role in various biochemical pathways, particularly in nucleic acid metabolism and cellular signaling. It may exhibit unique pharmacological properties, making it of interest in medicinal chemistry and biochemistry. The compound's solubility, reactivity, and interaction with biological macromolecules can differ from those of standard inosine, which may affect its therapeutic applications. Overall, carbocyclic inosine represents a significant area of study for researchers exploring nucleoside analogs and their implications in health and disease.
Formula:C11H14N4O4
InChI:InChI=1/C11H14N4O4/c16-2-5-1-6(9(18)8(5)17)15-4-14-7-10(15)12-3-13-11(7)19/h3-6,8-9,16-18H,1-2H2,(H,12,13,19)
SMILES:C1C(CO)C(C(C1n1cnc2c1ncnc2O)O)O
Synonyms:
  • Coaristeromycin
  • Nsc 103529
  • 6H-Purin-6-one, 9-(2,3-dihydroxy-4-(hydroxymethyl)cyclopentyl)-1,9-dihydro-, (1S-(1alpha,2beta,3beta,4alpha))-
  • 9-[(1R,2S,3R,4R)-2,3-dihydroxy-4-(hydroxymethyl)cyclopentyl]-3,9-dihydro-6H-purin-6-one
  • 9-[2,3-dihydroxy-4-(hydroxymethyl)cyclopentyl]-3,9-dihydro-6H-purin-6-one
  • Carbocyclic inosine
  • 9-((1R,2S,3R,4R)-2,3-Dihydroxy-4-(hydroxymethyl)cyclopentyl)-1H-purin-6(9H)-one
  • 6H-Purin-6-one, 9-[(1R,2S,3R,4R)-2,3-dihydroxy-4-(hydroxymethyl)cyclopentyl]-1,9-dihydro-
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Purity (%)
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100
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50
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90
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95
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100
Found 2 products.
  • Carbocyclic inosine

    CAS:
    <p>Carbocyclic inosine is a natural product that has been found to have inhibitory effects on the growth of mammalian cells and soil bacteria. It has been shown to be an analog of guanine, and it binds reversibly to the adenine-binding site of DNA. Carbocyclic inosine inhibits cell nuclei by preventing the formation of RNA and protein, which are essential for cell division. Carbocyclic inosine also inhibits the synthesis of DNA, RNA, and protein in mammalian cells. This agent has allelopathic properties that may be due to its ability to inhibit the growth of other plants.</p>
    Formula:C11H14N4O4
    Purity:Min. 95%
    Molecular weight:266.25 g/mol

    Ref: 3D-NC29205

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