| 词条 | Preakuammicine |
| 释义 | {{unreferenced|date=February 2015}}{{Chembox | ImageFile = Preakuammicine.svg | ImageSize = 200px | IUPACName = Methyl (16α,19E)-16-(hydroxymethyl)-1,2-didehydrocur-19-en-17-oate | OtherNames = |Section1={{Chembox Identifiers | CASNo = | PubChem = | ChemSpiderID = 29763444 | SMILES = C/C=C\\1/CN2CC[C@@]34[C@@H]2C[C@@H]1[C@](C3=Nc5c4cccc5)(CO)C(=O)OC | InChI = 1/C21H24N2O3/c1-3-13-11-23-9-8-20-14-6-4-5-7-16(14)22-18(20)21(12-24,19(25)26-2)15(13)10-17(20)23/h3-7,15,17,24H,8-12H2,1-2H3/b13-3-/t15-,17-,20+,21-/m0/s1 | InChIKey = DSOCELULQRKOMA-OQTQPSEIBY | StdInChI = 1S/C21H24N2O3/c1-3-13-11-23-9-8-20-14-6-4-5-7-16(14)22-18(20)21(12-24,19(25)26-2)15(13)10-17(20)23/h3-7,15,17,24H,8-12H2,1-2H3/b13-3-/t15-,17-,20+,21-/m0/s1 | StdInChIKey = DSOCELULQRKOMA-OQTQPSEISA-N |Section2={{Chembox Properties | C=21 | H=24 | N=2 | O=3 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} Preakuammicine is a terpene indole alkaloid. Preakuammicine is thought to be formed from 4,21-dehydrogeissoschizine and lead to synthesis of stemmadenine. The enzymes involved in preakuammicine formation and those which use it as a substrate are currently unknown. {{alkaloid-stub}} 1 : Indole alkaloids |
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