| 词条 | Vindoline |
| 释义 |
| ImageFile = Vindoline.svg | ImageSize = 200px | ImageAlt = | IUPACName = Methyl (2β,3β,4β,5α,12β,19α)-3,4-dihydroxy-16-methoxy-1-methyl-6,7-didehydroaspidospermidine-3-carboxylate | OtherNames = |Section1={{Chembox Identifiers | CASNo = 2182-14-1 | EINECS = 218-558-0 | PubChem = 260535 | ChemSpiderID = 228680 | SMILES = CC[C@@]12C=CCN3[C@@H]1[C@@]4(CC3)c5ccc(cc5N([C@H]4C([C@@H]2OC(=O)C)(C(=O)OC)O)C)OC | InChI = 1/C25H32N2O6/c1-6-23-10-7-12-27-13-11-24(19(23)27)17-9-8-16(31-4)14-18(17)26(3)20(24)25(30,22(29)32-5)21(23)33-15(2)28/h7-10,14,19-21,30H,6,11-13H2,1-5H3/t19-,20+,21+,23+,24+,25-/m0/s1 | InChIKey = CXBGOBGJHGGWIE-ACSXSLCXBW | StdInChI = 1S/C25H32N2O6/c1-6-23-10-7-12-27-13-11-24(19(23)27)17-9-8-16(31-4)14-18(17)26(3)20(24)25(30,22(29)32-5)21(23)33-15(2)28/h7-10,14,19-21,30H,6,11-13H2,1-5H3/t19-,20+,21+,23+,24+,25-/m0/s1 | StdInChIKey = CXBGOBGJHGGWIE-ACSXSLCXSA-N}} |Section2={{Chembox Properties | C=25 | H=32 | N=2 | O=6 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}Vindoline is a chemical precursor to vinblastine.[1] Vindoline is formed through biosynthesis from Tabersonine. References1. ^{{cite journal |pmid= 23864440 |year= 2014 |author1= Liu |first1= J |title= Enhancement of vindoline and vinblastine production in suspension-cultured cells of Catharanthus roseus by artemisinic acid elicitation |journal= World Journal of Microbiology and Biotechnology |volume= 30 |issue= 1 |pages= 175–80 |last2= Zhu |first2= J |last3= Tang |first3= L |last4= Wen |first4= W |last5= Lv |first5= S |last6= Yu |first6= R |doi= 10.1007/s11274-013-1432-z }} {{alkaloid-stub}} 1 : Indole alkaloids |
| 随便看 |
|
开放百科全书收录14589846条英语、德语、日语等多语种百科知识，基本涵盖了大多数领域的百科知识，是一部内容自由、开放的电子版国际百科全书。