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Resistomycin
Другие языки:

    Resistomycin

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    Resistomycin
    Resistomycin.png
    Names
    IUPAC name
    6,10,14,19-Tetrahydroxy-4,9,9-trimethylpentacyclo[13.3.1.05,18.08,17.011,16]nonadeca-1(19),3,5,7,10,13,15,17-octaene-2,12-dione
    Other names
      • Heliomycin
      • Geliomycin
      • Itamycin
      • 3,5,7,10-tetrahydroxy-1,1,9-trimethyl-2H-Benzo[cf]pyrene-2,6(1H)-dione
      • 3,5,7,10-tetrahydroxy-1,1,9-trimethyl-2H-Benzo[cd]pyrene-2,6(1H)-dione
      • 3,5,7,10-Tetrahydroxy-1,1,9-trimethyl-2H-benzo[cf]pyrene-2,6(1H)-dione
      • 3,5,7,10-Tetrahydroxy-1,1,9-trimethyl-1H-benzo[cd]pyrene-2,6-dione
    Identifiers
    3D model (JSmol)
    ChEBI
    ChEMBL
    PubChem CID
    • InChI=1S/C22H16O6/c1-7-4-9(23)15-18-13(7)10(24)5-8-14(18)19-16(20(15)27)11(25)6-12(26)17(19)21(28)22(8,2)3/h4-6,24-25,27-28H,1-3H3
      Key: MJKDGCARCYPVQG-UHFFFAOYSA-N
    • CC1(C)C2=C3C=4C(C(=O)C=5C3=C(C(O)=C2)C(C)=CC5O)=C(O)C=C(O)C4C1=O
    Properties
    C22H16O6
    Molar mass 376.364 g·mol−1
    Boiling point 315°C
    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    Resistomycin is an antibiotic with the molecular formula C22H16O6. Resistomycin is similar to hypericin. Resistomycin was first isolated in 1951 from the bacterium Streptomyces resistomycificus.

    Further reading

    • Brockmann, Hans; Meyer, Ernst; Schrempp, Klaus; Reiners, Fritz; Reschke, Till (April 1969). "Resistomycin, IV. Die Konstitution des Resistomycins". Chemische Berichte. 102 (4): 1224–1246. doi:10.1002/cber.19691020415. PMID 5802095.
    • Comprehensive Natural Products II: Chemistry and Biology. Elsevier. 5 March 2010. p. 266. ISBN 978-0-08-045382-8.



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