Flavipin: Difference between revisions
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Daniel-Brown (talk | contribs) ←Created page with '{{Chembox <!-- Images --> | ImageFile = | ImageSize = | ImageAlt = <!-- Names --> | IUPACName = 3,4,5-trihydroxy-6-methylphthalaldehyde<ref name=Flavipin>{{cite journal |title=Flavipin |journal=pubchem.ncbi.nlm.nih.gov |url=https://pubchem.ncbi.nlm.nih.gov/compound/Flavipin#section=3D-Conformer |language=en}}</ref> | OtherNames = <!-- Sections --> | Section1 = {{Chembox Identifiers | CASNo = 483-53-4 | CASNo_Ref =...' |
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Revision as of 03:03, 20 April 2022
| Names | |
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| IUPAC name
3,4,5-trihydroxy-6-methylphthalaldehyde[1]
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| Identifiers | |
PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C9H8O5 | |
| Molar mass | 196.158 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Flavipin is a phototoxic, antibiotic and antifungal metabolit with the molecular formula C9H8O5 which is produced by the fungi Aspergillus flavipes, Epicoccum nigrum and Epicoccum andropogonis.[2][1][3] Flavipin is also a potent antioxidant.[4]
References
- ^ a b "Flavipin". pubchem.ncbi.nlm.nih.gov.
- ^ Mücke, Wolfgang; Lemmen, Christa (2004). Schimmelpilze: Vorkommen, Gesundheitsgefahren, Schutzmaßnahmen (in German). ecomed-Storck GmbH. p. 30. ISBN 978-3-609-68001-9.
- ^ Bamford, P.C.; Norris, G.L.F.; Ward, G. (September 1961). "Flavipin production by Epicoccum spp". Transactions of the British Mycological Society. 44 (3): 354–356. doi:10.1016/S0007-1536(61)80028-4.
- ^ Ye, Yonghao; Xiao, Yu; Ma, Liang; Li, Hongxia; Xie, Zhenglu; Wang, Minghua; Ma, Haitian; Tang, Huaiwu; Liu, Junyan (August 2013). "Flavipin in Chaetomium globosum CDW7, an endophytic fungus from Ginkgo biloba, contributes to antioxidant activity". Applied Microbiology and Biotechnology. 97 (16): 7131–7139. doi:10.1007/s00253-013-5013-8.
Further reading
- Korzybski, Tadeusz; Kowszyk-Gindifer, Zuzanna; Kurylowicz, Wlodzimierz (3 September 2013). Antibiotics: Origin, Nature and Properties. Elsevier. p. 1285. ISBN 978-1-4832-2304-9.
- Abdel-Azeem, Ahmed M. (2021). Industrially Important Fungi for Sustainable Development: Volume 2: Bioprospecting for Biomolecules. Springer Nature. p. 135. ISBN 978-3-030-85603-8.
- Lloyd, D. (6 December 2012). Topics in Carbocyclic Chemistry: Volume One. Springer Science & Business Media. p. 90. ISBN 978-1-4684-8270-6.
- Nitao, James; Meyer, Susan; Chitwood, David; Schmidt, Walter; Oliver, James (2002). "Isolation of flavipin, a fungus compound antagonistic to plant-parasitic nematodes". Nematology. 4 (1): 55–63. doi:10.1163/156854102760082203.
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