| 词条 | Iridomyrmecin |
| 释义 |
| ImageFile = Iridomyrmecin.svg | ImageSize = 180px | IUPACName = (4S,4aS,7S,7aR)-4,7-dimethylhexahydrocyclopenta[c]pyran-3(1H)-one | OtherNames = Iridomyrmexin |Section1={{Chembox Identifiers | CASNo = 485-43-8 | CASNo_Ref = {{cascite|correct|CAS}} | PubChem = 442427 | ChemSpiderID = 390867 | SMILES = O=C1OC[C@@H]2[C@H](CC[C@@H]2[C@@H]1C)C | InChI = InChI=1S/C10H16O2/c1-6-3-4-8-7(2)10(11)12-5-9(6)8/h6-9H,3-5H2,1-2H3/t6-,7-,8+,9+/m0/s1 |Section2={{Chembox Properties | C=10 | H=16 | O=2 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}Iridomyrmecin is a defensive chemical, classified as an iridoid, isolated from ants of the genus Iridomyrmex.[1] Iridomyrmecin is also found in a variety of plants including Actinidia polygama.[2] See also
References1. ^{{cite journal | title = The chemistry of ants. I. Terpenoid constituents of some Australian Iridomyrmex species |author1=Cavill, G. W. K. |author2=Ford, D. L. |author3=Locksley, H. D. | journal = Australian Journal of Chemistry | year = 1956 | volume = 9 | pages = 288–293 | doi = 10.1071/CH9560288 | issue = 2}} {{organic-compound-stub}}2. ^{{cite journal |author1=Sakan, Takeo |author2=Isoe, Sachihiko |author3=Hyeon, Suong Be |author4=Katsumura, Ryuichi |author5=Maeda, Takashi |author6=Wolinsky, Joseph |author7=Dickerson, Dorsey |author8=Slabaugh, Michael |author9=Nelson, David | title = Exact nature of matatabilactone and the terpenes of Nepeta cataria | journal = Tetrahedron Letters | year = 1965 | volume = 46 | pages = 4097–4102 | doi=10.1016/s0040-4039(01)99572-3}} 3 : Iridoids|Lactones|Cyclopentanes |
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