| 词条 | Communesin B |
| 释义 |
| ImageFile = Communesin B.svg | ImageSize = 150px | ImageAlt = | IUPACName = | OtherNames = |Section1={{Chembox Identifiers | CASNo = | PubChem = 44575539 | ChemSpiderID = 24713764 | SMILES = C/C=C/C=C/C(=O)N1CC[C@]23[C@H]1N4CC[C@@]25c6c(cccc6N([C@H]5Nc7c3cccc7)C)[C@H]4[C@@H]8C(O8)(C)C | StdInChI = 1S/C32H36N4O2/c1-5-6-7-15-24(37)35-18-16-31-21-12-8-9-13-22(21)33-28-32(31)17-19-36(29(31)35)26(27-30(2,3)38-27)20-11-10-14-23(25(20)32)34(28)4/h5-15,26-29,33H,16-19H2,1-4H3/b6-5+,15-7+/t26-,27+,28+,29+,31-,32-/m0/s1 | StdInChIKey = XZFSMUXVAYCHFO-RPCCRITPSA-N}} |Section2={{Chembox Properties | C=32 | H=36 | N=4 | O=2 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}Communesin B is a cytotoxic fungi isolate.[1] References1. ^{{Cite journal | pmid = 12943379 | year = 2003 | last1 = Crawley | first1 = SL | last2 = Funk | first2 = RL | title = A synthetic approach to nomofungin/communesin B | volume = 5 | issue = 18 | pages = 3169–71 | doi = 10.1021/ol034407v | journal = Organic Letters}} {{organic-compound-stub}} 1 : Epoxides |
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