(Redirected from
Iso-Oosporein)
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| Names | |
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IUPAC name
2-(2,5-dihydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-3,6-dihydroxy-5-methylcyclohexa-2,5-diene-1,4-dione
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| Other names | |
| Identifiers | |
3D model (
JSmol)
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| ChemSpider | |
PubChem
CID
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| UNII | |
CompTox Dashboard (
EPA)
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| Properties | |
| C14H10O8 | |
| Molar mass | 306.226 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Oosporein is a toxic, bronze colored di benzoquinone with the molecular formula C14H10O8. [2] [3] Oosporein was first extracted from various molds and has antibiotic, [4] antiviral, cytotoxic, antifungal, and Insecticide properties. [3] [5] [2]
References
- ^ "Oosporein (CAS 475-54-7)". www.caymanchem.com.
- ^ a b c d Eisenbrand, Gerhard; Schreier, Peter (14 May 2014). RÖMPP Lexikon Lebensmittelchemie, 2. Auflage, 2006 (in German). Georg Thieme Verlag. p. 824. ISBN 978-3-13-179282-2.
- ^ a b Feng, Peng; Shang, Yanfang; Cen, Kai; Wang, Chengshu (8 September 2015). "Fungal biosynthesis of the bibenzoquinone oosporein to evade insect immunity". Proceedings of the National Academy of Sciences. 112 (36): 11365–11370. doi: 10.1073/pnas.1503200112. PMC 4568701. PMID 26305932.
- ^ Handbook of Applied Mycology: Volume 2: Humans, Animals and Insects. CRC Press. 25 July 1991. p. 626. ISBN 978-0-8247-8435-5.
- ^ Ramesha, Alurappa; Venkataramana, M.; Nirmaladevi, Dhamodaran; Gupta, Vijai K.; Chandranayaka, S.; Srinivas, Chowdappa (1 September 2015). "Cytotoxic effects of oosporein isolated from endophytic fungus Cochliobolus kusanoi". Frontiers in Microbiology. 6: 870. doi: 10.3389/fmicb.2015.00870. PMC 4556033. PMID 26388840.
Further reading
- Mc Namara, Louise; Dolan, Stephen K.; Walsh, John M.D.; Stephens, John C.; Glare, Travis R.; Kavanagh, Kevin; Griffin, Christine T. (August 2019). "Oosporein, an abundant metabolite in Beauveria caledonica, with a feedback induction mechanism and a role in insect virulence" (PDF). Fungal Biology. 123 (8): 601–610. doi: 10.1016/j.funbio.2019.01.004. PMID 31345414. S2CID 92167627.
- Kögl, F.; van Wessem, G. C. (1944). "Untersuchungen über Pilzfarbstoffe XIV : Über Oosporein, den Farbstoff von Oospora colorans van Beyma". Recueil des Travaux Chimiques des Pays-Bas. 63 (1): 5–12. doi: 10.1002/recl.19440630102.
- Ross, P. Frank; Osheim, David L.; Rottinghaus, George E. (July 1989). "Mass Spectral Confirmation of Oosporein in Poultry Rations". Journal of Veterinary Diagnostic Investigation. 1 (3): 271–272. doi: 10.1177/104063878900100317. PMID 2488354.
- Canadian Journal of Biochemistry. National Research Council of Canada. p. 562.
- Smith, DUPLICATE; Henderson, Rachel (23 July 1991). Mycotoxins and Animal Foods. CRC Press. p. 586. ISBN 978-0-8493-4904-1.
 | This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
(Redirected from
Iso-Oosporein)
|
| |
| Names | |
|---|---|
|
IUPAC name
2-(2,5-dihydroxy-4-methyl-3,6-dioxocyclohexa-1,4-dien-1-yl)-3,6-dihydroxy-5-methylcyclohexa-2,5-diene-1,4-dione
| |
| Other names | |
| Identifiers | |
3D model (
JSmol)
|
|
| ChemSpider | |
PubChem
CID
|
|
| UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
| Properties | |
| C14H10O8 | |
| Molar mass | 306.226 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
| |
Oosporein is a toxic, bronze colored di benzoquinone with the molecular formula C14H10O8. [2] [3] Oosporein was first extracted from various molds and has antibiotic, [4] antiviral, cytotoxic, antifungal, and Insecticide properties. [3] [5] [2]
References
- ^ "Oosporein (CAS 475-54-7)". www.caymanchem.com.
- ^ a b c d Eisenbrand, Gerhard; Schreier, Peter (14 May 2014). RÖMPP Lexikon Lebensmittelchemie, 2. Auflage, 2006 (in German). Georg Thieme Verlag. p. 824. ISBN 978-3-13-179282-2.
- ^ a b Feng, Peng; Shang, Yanfang; Cen, Kai; Wang, Chengshu (8 September 2015). "Fungal biosynthesis of the bibenzoquinone oosporein to evade insect immunity". Proceedings of the National Academy of Sciences. 112 (36): 11365–11370. doi: 10.1073/pnas.1503200112. PMC 4568701. PMID 26305932.
- ^ Handbook of Applied Mycology: Volume 2: Humans, Animals and Insects. CRC Press. 25 July 1991. p. 626. ISBN 978-0-8247-8435-5.
- ^ Ramesha, Alurappa; Venkataramana, M.; Nirmaladevi, Dhamodaran; Gupta, Vijai K.; Chandranayaka, S.; Srinivas, Chowdappa (1 September 2015). "Cytotoxic effects of oosporein isolated from endophytic fungus Cochliobolus kusanoi". Frontiers in Microbiology. 6: 870. doi: 10.3389/fmicb.2015.00870. PMC 4556033. PMID 26388840.
Further reading
- Mc Namara, Louise; Dolan, Stephen K.; Walsh, John M.D.; Stephens, John C.; Glare, Travis R.; Kavanagh, Kevin; Griffin, Christine T. (August 2019). "Oosporein, an abundant metabolite in Beauveria caledonica, with a feedback induction mechanism and a role in insect virulence" (PDF). Fungal Biology. 123 (8): 601–610. doi: 10.1016/j.funbio.2019.01.004. PMID 31345414. S2CID 92167627.
- Kögl, F.; van Wessem, G. C. (1944). "Untersuchungen über Pilzfarbstoffe XIV : Über Oosporein, den Farbstoff von Oospora colorans van Beyma". Recueil des Travaux Chimiques des Pays-Bas. 63 (1): 5–12. doi: 10.1002/recl.19440630102.
- Ross, P. Frank; Osheim, David L.; Rottinghaus, George E. (July 1989). "Mass Spectral Confirmation of Oosporein in Poultry Rations". Journal of Veterinary Diagnostic Investigation. 1 (3): 271–272. doi: 10.1177/104063878900100317. PMID 2488354.
- Canadian Journal of Biochemistry. National Research Council of Canada. p. 562.
- Smith, DUPLICATE; Henderson, Rachel (23 July 1991). Mycotoxins and Animal Foods. CRC Press. p. 586. ISBN 978-0-8493-4904-1.
|
| This article about an organic compound is a stub. You can help Wikipedia by expanding it. |