| 词条 | Corynoline |
| 释义 |
| ImageFile = Corynoline.svg | ImageSize = 150px | ImageAlt = | IUPACName = | OtherNames = 13-Methylchelidonine |Section1={{Chembox Identifiers | CASNo = | PubChem = 177014 | ChemSpiderID = 154159 | SMILES = O1c2c(OC1)c3c(cc2)[C@@]5([C@H](N(C3)C)c4cc6OCOc6cc4C[C@@H]5O)C | InChI = 1/C21H21NO5/c1-21-14-3-4-15-19(27-10-24-15)13(14)8-22(2)20(21)12-7-17-16(25-9-26-17)5-11(12)6-18(21)23/h3-5,7,18,20,23H,6,8-10H2,1-2H3/t18-,20+,21-/m0/s1 | InChIKey = IQUGPRHKZNCHGC-TYPHKJRUBF | StdInChI = 1S/C21H21NO5/c1-21-14-3-4-15-19(27-10-24-15)13(14)8-22(2)20(21)12-7-17-16(25-9-26-17)5-11(12)6-18(21)23/h3-5,7,18,20,23H,6,8-10H2,1-2H3/t18-,20+,21-/m0/s1 | StdInChIKey = IQUGPRHKZNCHGC-TYPHKJRUSA-N }} |Section2={{Chembox Properties | C=21 | H=21 | N=1 | O=5 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}Corynoline is an acetylcholinesterase inhibitor isolated from Corydalis incisa.[1] References1. ^{{cite journal|pmid=12510831 |year=2002|last1=Kim|first1=DK|title=Inhibitory effect of corynoline isolated from the aerial parts of Corydalis incisa on the acetylcholinesterase|volume=25|issue=6|pages=817–9|journal=Archives of Pharmacal Research|doi=10.1007/bf02976997}} {{Acetylcholine metabolism and transport modulators}}{{organic-compound-stub}} 2 : Acetylcholinesterase inhibitors|Alkaloids |
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