Cyclanoline

Cyclanoline
Names
Other names
Cissamine
Identifiers
CAS Number
  • 18556-27-9 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:76923
ChemSpider
  • 2339606
PubChem CID
  • 3082134
UNII
  • 77QC59KBD2 checkY
CompTox Dashboard (EPA)
  • DTXSID00171789 Edit this at Wikidata
InChI
  • InChI=1S/C20H23NO4/c1-21-7-6-13-9-19(25-3)17(22)10-14(13)16(21)8-12-4-5-18(24-2)20(23)15(12)11-21/h4-5,9-10,16H,6-8,11H2,1-3H3,(H-,22,23)/p+1/t16-,21-/m0/s1
    Key: LKLWVKCEYSPQHL-KKSFZXQISA-O
  • COc1ccc2C[C@H]3c4cc(O)c(OC)cc4CC[N@@+]3(C)Cc2c1O
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Cyclanoline is an acetylcholinesterase inhibitor isolated from Stephania venosa tuber.[1]


References

  1. ^ Ingkaninan, Kornkanok; Phengpa, Preeda; Yuenyongsawad, Supreeya; Khorana, Nantaka (2006). "Acetylcholinesterase inhibitors from Stephania venosa tuber". Journal of Pharmacy and Pharmacology. 58 (5): 695–700. doi:10.1211/jpp.58.5.0015. PMID 16640839. S2CID 25176455.


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Acetylcholine metabolism and transport modulators
Enzyme
(modulators)
ChATTooltip Choline acetyltransferase
  • Inhibitors: 1-(-Benzoylethyl)pyridinium
  • 2-(α-Naphthoyl)ethyltrimethylammonium
  • 3-Chloro-4-stillbazole
  • 4-(1-Naphthylvinyl)pyridine
  • Acetylseco hemicholinium-3
  • Acryloylcholine
  • AF64A
  • B115
  • BETA
  • CM-54,903
  • N,N-Dimethylaminoethylacrylate
  • N,N-Dimethylaminoethylchloroacetate
AChETooltip Acetylcholinesterase
BChETooltip Butyrylcholinesterase
Transporter
(modulators)
CHTTooltip Choline transporter
VAChTTooltip Vesicular acetylcholine transporter
Release
(modulators)
Inhibitors
  • SNAP-25Tooltip Synaptosomal-associated protein 25 inactivators: Botulinum toxin (A, C, E)
  • VAMPTooltip Vesicle-associated membrane protein inactivators: Botulinum toxin (B, D, F, G)
Enhancers
See also
Receptor/signaling modulators
Muscarinic acetylcholine receptor modulators
Nicotinic acetylcholine receptor modulators


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