Aquayamycin
rot oranger Feststoff[1]
| Strukturformel | |||||||||||||
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| Allgemeines | |||||||||||||
| Name | Aquayamycin | ||||||||||||
| Summenformel | C25H26O10 | ||||||||||||
| Kurzbeschreibung |
rot oranger Feststoff[1] | ||||||||||||
| Externe Identifikatoren/Datenbanken | |||||||||||||
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| Eigenschaften | |||||||||||||
| Molare Masse | 486,47 g·mol−1 | ||||||||||||
| Aggregatzustand |
fest[1] | ||||||||||||
| Schmelzpunkt | |||||||||||||
| Sicherheitshinweise | |||||||||||||
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| Wenn nicht anders vermerkt, gelten die angegebenen Daten bei Standardbedingungen (0 °C, 1000 hPa). | |||||||||||||
Aquayamycin gehört zur Gruppe der Angucycline und wird aus Streptomyces isoliert. Es ist ein Hydrolyseprodukt von Vineomycin A1.[1]
Literatur
- M. Sezaki, S. Kondo, K. Maeda, H. Umezawa, M. Ono: The structure of aquayamycin, Tetrahedron, 1970, 26 (22), S. 5171–5190. PMID 5499897. doi:10.1016/S0040-4020(01)98726-5.
- S. Kusumi, H. Nakayama, T. Kobayashi, H. Kuriki, Y. Matsumoto, D. Takahashi, K. Toshima: Total Synthesis of Aquayamycin, Chem. Eur. J., 2016, 22, S. 18733–18736; doi:10.1002/chem.201604697.
Einzelnachweise
- ↑ a b c d Barrie W. Bycroft: Dictionary of Antibiotics & Related Substances. CRC Press, 1987, ISBN 978-0-412-25450-5, S. 131 (books.google.de).
- ↑ Dieser Stoff wurde in Bezug auf seine Gefährlichkeit entweder noch nicht eingestuft oder eine verlässliche und zitierfähige Quelle hierzu wurde noch nicht gefunden.
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