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Corynoline

From Wikipedia, the free encyclopedia
Corynoline
Names
IUPAC name
13-Methylchelidonine
Systematic IUPAC name
(5bR,6S,12bR)-5b,13-Dimethyl-5b,6,7,12b,13,14-hexahydro-2H,10H-[1,3]benzodioxolo[5,6-c][1,3]dioxolo[4,5-h]phenanthridin-6-ol
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard100.208.689Edit this at Wikidata
EC Number
  • 683-177-2
UNII
  • InChI=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
    Key: IQUGPRHKZNCHGC-TYPHKJRUSA-N
  • 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
    Key: IQUGPRHKZNCHGC-TYPHKJRUBF
  • O1c2c(OC1)c3c(cc2)[C@@]5([C@H](N(C3)C)c4cc6OCOc6cc4C[C@@H]5O)C
Properties
C21H21NO5
Molar mass367.401 g·mol−1
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Corynoline is anacetylcholinesterase inhibitor isolated fromCorydalis incisa.[1]

References

[edit]
  1. ^Kim, DK (2002). "Inhibitory effect of corynoline isolated from the aerial parts of Corydalis incisa on the acetylcholinesterase".Archives of Pharmacal Research.25 (6):817–9.doi:10.1007/bf02976997.PMID 12510831.S2CID 35891875.
Enzyme
(modulators)
ChATTooltip Choline acetyltransferase
AChETooltip Acetylcholinesterase
BChETooltip Butyrylcholinesterase
Transporter
(modulators)
CHTTooltip Choline transporter
VAChTTooltip Vesicular acetylcholine transporter
Release
(modulators)
Inhibitors
Enhancers


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