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Names

18-Methoxycoronaridine
18-MC

IUPAC names

Methyl 21-methoxyibogamine-18-carboxylate
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

ID 3626 · Formula C₂₂H₂₈N₂O₃ · Molecular weight 368.469

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 This stereoisomer Any stereoisomer

SMILES COCC[C@H]1C[C@H]2CN3[C@@H]1[C@](C2)(C(=O)OC)c1[nH]c2c(c1CC3)cccc2

ChemSpider 24721799
PubChem 15479177
Wikipedia 18-Methoxycoronaridine

Wasko, M; Witt-Enderby, PA; Surratt, CK. DARK classics in chemical neuroscience: Ibogaine ACS Chem. Neurosci., 17 Oct 2018, 9 (10), 2475–2483. 5.1 MB. https://doi.org/10.1021/acschemneuro.8b00294 #18-MC

Arias, HR; Feuerbach, D; Targowska-Duda, KM; Jozwiak, K. Structure–activity relationship of ibogaine analogs interacting with nicotinic acetylcholine receptors in different conformational states Int. J. Biochem. Cell Biol., 1 Sep 2011, 43 (9), 1330–1339. 1.1 MB. https://doi.org/10.1016/j.biocel.2011.05.011 #18-Methoxycoronaridine

Cumming, P; Scheidegger, M; Dornbierer, D; Palner, M; Quednow, BB; Martin-Soelch, C. Molecular and functional imaging studies of psychedelic drug action in animals and humans Molecules, 1 Jan 2021, 26 (9), 2451. 3.5 MB. https://doi.org/10.3390/molecules26092451 #19

N-(2,5-Dimethoxyphenylethyl)-5-MeO-NMT · N-(2,5-Dimethoxyphenylethyl)-5-methoxy-N-methyltryptamine

N-(3,4-Dimethoxyphenylethyl)-5-MeO-NMT · N-(3,4-Dimethoxyphenylethyl)-5-methoxy-N-methyltryptamine

Corynantheidine

JTE 7-31

WO 2005/016351 #13-044

9992

Isocorynantheidine

Voacangine

14560

7 Dec 2019 · · Isomer Design