| 词条 | Setoclavine |
| 释义 |
| ImageFile = Setoclavine.svg | ImageSize = 150px | ImageAlt = | SystematicName = (8α)-6,8-Dimethyl-9,10-didehydroergolin-8-ol | OtherNames = |Section1={{Chembox Identifiers | CASNo = 519-12-0 | PubChem = 11482216 | ChemSpiderID = 9657036 | SMILES = O[C@]3(/C=C2/c4cccc1c4c(c[nH]1)C[C@H]2N(C3)C)C | InChI=1S/C16H18N2O/c1-16(19)7-12-11-4-3-5-13-15(11)10(8-17-13)6-14(12)18(2)9-16/h3-5,7-8,14,17,19H,6,9H2,1-2H3/t14-,16+/m1/s1 | InChIKey=BGVUWLLRNRBDAY-ZBFHGGJFSA-N }} |Section2={{Chembox Properties | C=16 | H=18 | N=2 | O=1 | Appearance = prisms | Density = | MeltingPtC = 229 to 234 [1] | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}Setoclavine is an ergot alkaloid.[2] References1. ^J. E. Saxton (1960). "The Indole Alkaloids". In The Alkaloids, Vol. VII, (R. H. F. Manske, Ed.), pp. 4-183, New York: Academic Press. {{alkaloid-stub}}2. ^{{cite journal|pmid=11414824|year=2001|last1=Liras|first1=S|last2=Lynch|first2=CL|last3=Fryer|first3=AM|last4=Vu|first4=BT|last5=Martin|first5=SF|title=Applications of vinylogous Mannich reactions. Total syntheses of the Ergot alkaloids rugulovasines a and B and setoclavine|volume=123|issue=25|pages=5918–24|journal=Journal of the American Chemical Society|doi=10.1021/ja010577w}} 1 : Ergot alkaloids |
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