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Antibiotic
Angustmycin A
Другие языки:

    Angustmycin A

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    Angustmycin A
    Decoyinine.svg
    Names
    IUPAC name
    2-(6-aminopurin-9-yl)-2-(hydroxymethyl)-5-methylideneoxolane-3,4-diol
    Other names
    Decoyinine
    4′,5′-Didehydro-1′-C-(hydroxymethyl)adenosine
    Identifiers
    3D model (JSmol)
    ChEMBL
    ChemSpider
    ECHA InfoCard 100.213.257
    EC Number
    • 687-357-1
    PubChem CID
    • InChI=1S/C11H13N5O4/c1-5-7(18)8(19)11(2-17,20-5)16-4-15-6-9(12)13-3-14-10(6)16/h3-4,7-8,17-19H,1-2H2,(H2,12,13,14)
      Key: UZSSGAOAYPICBZ-UHFFFAOYSA-N
    • C=C1[C@H]([C@H]([C@](O1)(CO)N2C=NC3=C(N=CN=C32)N)O)O
    Properties
    C11H13N5O4
    Molar mass 279.256 g·mol−1
    Hazards
    GHS labelling:
    GHS07: Exclamation mark
    Warning
    H315, H319, H335
    P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501
    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    Angustmycin A is a purine antibiotic and metabolite from Streptomyces bacteria with the molecular formula C11H13N5O4. Angustmycin A is also a cytokinin.

    Further reading

    • Hoeksema, H.; Slomp, G.; van Tamelen, E. E. (1 January 1964). "Angustmycin A and decoyinine". Tetrahedron Letters. 5 (27): 1787–1795. doi:10.1016/S0040-4039(01)89489-2. ISSN 0040-4039.
    • McCarthy, James R.; Robins, Roland K.; Robins, Morris J. (August 1968). "Purine nucleosides. XXII. Synthesis of angustmycin A (decoyinine) and related unsaturated nucleosides". Journal of the American Chemical Society. 90 (18): 4993–4999. doi:10.1021/ja01020a038.

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