18-Methoxycoronaridine

From Food & Medicine Encyclopedia

What is 18-Methoxycoronaridine?[edit]

18-Methoxycoronaridine
  • It is a α3β4 nicotinic antagonist.
  • IUPAC Name: methyl (1S,15R,17R,18S)-17-(2-methoxyethyl)-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate
  • InChI: InChI=1S/C22H28N2O3/c1-26-10-8-15-11-14-12-22(21(25)27-2)19-17(7-9-24(13-14)20(15)22)16-5-3-4-6-18(16)23-19/h3-6,14-15,20,23H,7-13H2,1-2H3/t14-,15+,20+,22-/m1/s1
  • InChI Key: DTJQBBHYRQYDEG-SVBQBFEESA-N
  • Canonical SMILES: COCCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC
  • Isomeric SMILES: COCC[C@H]1C[C@@H]2C[C@@]3([C@H]1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC
  • Molecular formula: C22H28N2O3
  • Molecular weight: 368.5 g·mol−1
  • PubChem CID: 15479177
  • Synonyms:
  1. UNII-KX8NQX91Z8
  2. KX8NQX91Z8
  3. 308123-60-6
  4. methyl (6S,6aS,7R,9R)-7-(2-methoxyethyl)-7,8,9,10,12,13-hexahydro-5H-6,9-methanopyrido[1',2':1,2]azepino[4,5-b]indole-6(6aH)-carboxylate
  5. 18-MC compound
  6. (+/-)-18-Methoxycoronaridine
  7. 18-Methoxycoronaridine, (+/-)-
  8. Ibogamine-18-carboxylic acid, 21-methoxy-, methyl ester
  9. Ibogamine-18-carboxylic acid, 21-methoxy-, methyl ester, (+/-)-
  10. DB15096
  11. 188125-42-0
  12. UNII-VG463BM9RL component DTJQBBHYRQYDEG-SVBQBFEESA-N
  13. (2R,4R,4aS,12bS)-4-(2-Methoxyethyl)-1,2,3,4,4a,5,6,7,12,12b-decahydro-2,5-methanoindolo[3,2-d][1]benzazepine-12b-carboxylic acid methyl ester

<ref>National Center for Biotechnology Information (2021). PubChem Compound Summary for CID 15479177, 18-Methoxycoronaridine, (+/-)-. Retrieved August 6, 2021 from [1].</ref>

References[edit]

Template:Nicotinic acetylcholine receptor modulators



This article is a stub related to pharmacology. You can help WikiMD by expanding it!

Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.