保幼酮
外觀
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保幼酮 | |
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IUPAC名 Methyl (4R)-4-[(2R)-6-methyl-4-oxoheptan-2-yl]cyclohex-1-ene-1-carboxylate | |
識別 | |
CAS號 | 17904-27-7 |
PubChem | 442381 |
ChemSpider | 390830 |
SMILES |
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InChI |
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InChIKey | IIWNDLDEVPJIBT-OLZOCXBDBI |
性質 | |
化學式 | C16H26O3 |
摩爾質量 | 266.38 g·mol−1 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
保幼酮(英語:Juvabione)是一種有機化合物,化學式C16H26O3,能視為倍半萜椴松酸的甲酯,屬於昆蟲保幼激素的相似物,由植物合成抵禦昆蟲。[1][2][3][4][5][6][7]
參考文獻
[編輯]- ^ Manville, J. F.; Kriz, C. D. Juvabione and its analogues. IV. Isolation, identification, and occurrence of juvabione, juvabiol, epijuvabiol from the whole wood of Abies lasiocarpa. Can. J. Chem. 1977, 55: 2547–2553. doi:10.1139/v77-351 .
- ^ Manville, J. F. Juvabione and its analogues. Juvabione and delta4'-dehydrojuvabione isolated from the whole wood of Abies balsamea, have the R>R stereoconfigurations, not R,S. Can. J. Chem. 1975, 53: 1579–1585. doi:10.1139/v75-223 .
- ^ Bohlmann, J.; Crock, J.; Jetter, R.; Croteau, R. Terpenoid-based defenses in conifers: cDNA cloning, characterization, and functional expression of wound-inducible (E)-alpha-bisabolene synthase from grand fir (Abies grandis). Proc. Natl. Acad. Sci. USA. 1998, 95 (12): 6756–6761. Bibcode:1998PNAS...95.6756B. PMC 22624 . PMID 9618485. doi:10.1073/pnas.95.12.6756 .
- ^ Phillips, M. A; Bohlmann, J.; Gershenzon, J. Molecular regulation of induced terpenoid biosynthesis in conifers. Phytochemistry Reviews. 2006, 55 (5): 179–189. S2CID 25713264. doi:10.1007/s11101-006-0001-6.
- ^ Bohlmann, J.; Meyer-Gauen, G.; Croteau, R. Plant terpenoid synthases: Molecular biology and phylogenetic analysis. Proc. Natl. Acad. Sci. USA. 1998, 95 (8): 4126–4133. Bibcode:1998PNAS...95.4126B. PMC 22453 . PMID 9539701. doi:10.1073/pnas.95.8.4126 .
- ^ Steele, C. L.; Crock, J.; Bohlmann, J.; Croteau, R. Sesquiterpene Synthases from Grand Fir (Abies grandis). J. Biol. Chem. 1998, 273 (4): 2078–2089. PMID 9442047. doi:10.1074/jbc.273.4.2078 .
- ^ Higuchi, T. Biosynthesis and biodegradation of wood components. Academic Press. 1985: 380–429.