Chemistry:Myrotoxin B
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Revision as of 22:52, 30 June 2021 by imported>AnLinks (correction)
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3D model (JSmol)
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PubChem CID
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Properties | |
C29H34O11 | |
Molar mass | 558.580 g·mol−1 |
Melting point | 195 to 197 °C (383 to 387 °F; 468 to 470 K)[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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Infobox references | |
Myrotoxin B is a macrocyclic trichothecene first isolated in 1985.[1] It was tested on Swiss mice and found to be very toxic, though not the most toxic of the three toxins that were tested at that time.[2] It has also been isolated from Myrothecium roridum, a pathogen leaf spot that affects mulberry, though it is unknown if it is used as a pathotoxin.[3]
References
- ↑ 1.0 1.1 Jarvis, B. B.; Lee, Y.-W.; Cömezoḡlu, F. T.; Cömezoḡlu, S. N.; Bean, G. A. (1985). "Myrotoxins: a new class of macrocyclic trichothecenes". Tetrahedron Letters 26 (40): 4859–62. doi:10.1016/S0040-4039(00)94970-0.
- ↑ Schiefer, H. B.; Hancock, D. S.; Jarvis, B. B. (1989). "Toxicology of Novel Macrocyclic Trichothecenes, Baccharinoid B4, Myrotoxin B, and Roritoxin B". Zentralblatt für Veterinärmedizin. Reihe A 36 (2): 152–60. doi:10.1111/j.1439-0442.1989.tb00715.x. ISSN 0514-7158. PMID 2501953.
- ↑ Murakami, R.; Shirata, A. (2005). "Myrotoxin B Detection from Mulberry Leaves Infected with Myrothecium roridum, cause Myrothecium Leaf Spot of Mulberry, and Possible Roles in Pathogenicity" (pdf). Japanese Journal of Phytopathology 71 (2): 91–100. doi:10.3186/jjphytopath.71.91. https://www.jstage.jst.go.jp/article/jjphytopath1918/71/2/71_2_91/_pdf.
![]() | Original source: https://en.wikipedia.org/wiki/Myrotoxin B.
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