18-Methylaminocoronaridine

18-Methylaminocoronaridine
Identifiers
PubChem CID	44325016;
ChemSpider	24721797 ;
Chemical and physical data
Formula	C22H29N3O2
Molar mass	367.493 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES c4cccc1c4c3c1CCN2CC(C5)CC3(C(=O)OC)C2C5CCNC;
	InChI InChI=1S/C22H29N3O2/c1-23-9-7-15-11-14-12-22(21(26)27-2)19-17(8-10-25(13-14)20(15)22)16-5-3-4-6-18(16)24-19/h3-6,14-15,20,23-24H,7-13H2,1-2H3/t14-,15+,20+,22-/m1/s1 ; Key:YKMOJVPLIUXEIP-SVBQBFEESA-N ;
	(verify)

(−)-18-Methylaminocoronaridine (18-MAC) is a second generation synthetic derivative of ibogaine developed by the research team led by the pharmacologist Stanley D. Glick from the Albany Medical College and the chemist Martin E. Kuehne from the University of Vermont.^[1]^[2]

References

^ Kuehne ME, He L, Jokiel PA, Pace CJ, Fleck MW, Maisonneuve IM, et al. (June 2003). "Synthesis and biological evaluation of 18-methoxycoronaridine congeners. Potential antiaddiction agents". Journal of Medicinal Chemistry. 46 (13): 2716–30. doi:10.1021/jm020562o. PMID 12801235.
^ Pace CJ, Glick SD, Maisonneuve IM, He LW, Jokiel PA, Kuehne ME, Fleck MW (May 2004). "Novel iboga alkaloid congeners block nicotinic receptors and reduce drug self-administration". European Journal of Pharmacology. 492 (2–3): 159–67. doi:10.1016/j.ejphar.2004.03.062. PMID 15178360.

Zdroj:https://en.wikipedia.org?pojem=18-Methylaminocoronaridine
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[1] Kuehne ME, He L, Jokiel PA, Pace CJ, Fleck MW, Maisonneuve IM, et al. (June 2003). "Synthesis and biological evaluation of 18-methoxycoronaridine congeners. Potential antiaddiction agents". Journal of Medicinal Chemistry. 46 (13): 2716–30. doi:10.1021/jm020562o. PMID 12801235.

[2] Pace CJ, Glick SD, Maisonneuve IM, He LW, Jokiel PA, Kuehne ME, Fleck MW (May 2004). "Novel iboga alkaloid congeners block nicotinic receptors and reduce drug self-administration". European Journal of Pharmacology. 492 (2–3): 159–67. doi:10.1016/j.ejphar.2004.03.062. PMID 15178360.

[1]

[2]

Identifiers

PubChem CID	44325016
ChemSpider	24721797^Y
Chemical and physical data
Formula	C₂₂H₂₉N₃O₂
Molar mass	367.493 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES c4cccc1c4c3c1CCN2CC(C5)CC3(C(=O)OC)C2C5CCNC
InChI InChI=1S/C22H29N3O2/c1-23-9-7-15-11-14-12-22(21(26)27-2)19-17(8-10-25(13-14)20(15)22)16-5-3-4-6-18(16)24-19/h3-6,14-15,20,23-24H,7-13H2,1-2H3/t14-,15+,20+,22-/m1/s1^Y Key:YKMOJVPLIUXEIP-SVBQBFEESA-N^Y
(verify)

See also

References