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| | botryodiplodin Basic information |
| Product Name: | botryodiplodin | | Synonyms: | botryodiplodin;1-(2-Hydroxy-3-methyltetrahydrofuran-4-yl)ethanone;4-Acetyl-2-hydroxy-3-methyltetrahydrofuran;4-Acetyltetrahydro-3-methylfuran-2-ol;Ethanone, 1-[(3S,4R)-tetrahydro-5-hydroxy-4-methyl-3-furanyl]-;Antibiotic PSX 1;Cytostipin | | CAS: | 27098-03-9 | | MF: | C7H12O3 | | MW: | 144.17 | | EINECS: | | | Product Categories: | | | Mol File: | 27098-03-9.mol |  |
| | botryodiplodin Chemical Properties |
| Melting point | 51°C | | Boiling point | 202.77°C (rough estimate) | | density | 1.0789 (rough estimate) | | refractive index | 1.4850 (estimate) | | pka | 12.79±0.60(Predicted) | | LogP | 0.571 (est) |
| | botryodiplodin Usage And Synthesis |
| Uses | Botryodiplodin is a mycotoxin isolated from Penicillium roqueforti. Botryodiplodin inhibits the growth of some Gram-positive and Gram-negative bacteria and can also induce DNA-protein cross-links in mammalian cells, inhibiting the synthesis of DNA, RNA, and protein[1][2]. | | Definition | ChEBI: Botryodiplodin is a member of oxolanes. | | References | [1] Moulé Y, et al. DNA-protein cross-linking by the mycotoxin, botryodiplodin, in mammalian cells[J]. Carcinogenesis, 1982, 3(2): 211-214. DOI:10.1093/carcin/3.2.211
[2] Moulé Y, et al. Mutagenicity of the mycotoxin botryodiplodin in the Salmonella typhimurium/microsomal activation test[J]. Environmental Mutagenesis, 1981, 3(3): 287-291. DOI:10.1002/em.2860030311 |
| | botryodiplodin Preparation Products And Raw materials |
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