Chemistry:Phlebiarubrone
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Names | |
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IUPAC name
4,7-diphenyl-1,3-benzodioxole-5,6-dione[1]
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Identifiers | |
3D model (JSmol)
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PubChem CID
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Properties | |
C19H12O4 | |
Molar mass | 304.301 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Tracking categories (test):
Phlebiarubrone is an antibiotic with the molecular formula C19H12O4 which is produced by the fungi Punctularia strigosozonata.[1][2][3][4][5][6]
References
- ↑ 1.0 1.1 "4,7-Diphenyl-1,3-benzodioxole-5,6-dione" (in en). Pubchem.ncbi.NLM.nih.gov. https://pubchem.ncbi.nlm.nih.gov/compound/12314165#section=Names-and-Identifiers.
- ↑ Bose, Ajay K.; Khanchandani, K. S.; Funke, P. T.; Anchel, Marjorie (1 January 1969). "Biosynthesis of phlebiarubrone in Phlebia strigosozonata" (in en). Journal of the Chemical Society D: Chemical Communications (22): 1347–1348. doi:10.1039/C29690001347. ISSN 0577-6171.
- ↑ (in en) Studies in Natural Products Chemistry: Bioactive Natural Products (Part J). Elsevier. 3 December 2003. p. 285. ISBN 978-0-08-054207-2.
- ↑ Rahman, Atta-ur (2003) (in en). Studies in Natural Products Chemistry: Bioactive Natural Products (Part J). Elsevier. p. 286. ISBN 978-0-08-054207-2.
- ↑ Bose, Ajay K.; Khanchandani, K. S.; Funke, P. T.; Anchel, Marjorie (1969). Biosynthesis of phlebiarubrone in Phlebia strigosozonata. pp. 1347–1348.
- ↑ Buckingham, John (1987). Dictionary of Organic Compounds. Taylor & Francis. p. 566. ISBN 978-0-412-17050-8.
Further reading
- Dallacker, Franz; Ditgens, Klaus (1 February 1975). "Synthese des Phlebiarubrons und der Polyporsäure / The Syntheses of Phlebiarubrone and Polyporic Acid" (in en). Zeitschrift für Naturforschung C 30 (1–2): 1–3. doi:10.1515/znc-1975-1-203. ISSN 1865-7125.
- Thomson, R. (2 December 2012) (in en). Naturally Occurring Quinones. Elsevier. p. 156. ISBN 978-0-323-16134-3.
Original source: https://en.wikipedia.org/wiki/Phlebiarubrone.
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