Homochiral structures derived from 1-[1-(2-thienyl)cyclohexyl]piperidine (TCP) are potent non-competitive antagonists of glutamate at NMDA receptor sites

DOI: 10.1016/0223-5234(94)90109-0

Source and publish data:

European Journal of Medicinal Chemistry p. 869 - 876 (1994)

Update date:2022-08-03

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Authors:

Michaud Michaud

Warren Warren

Drian Drian

Rambaud Rambaud

Cerruti Cerruti

Nicolas Nicolas

Vignon Vignon

Privat Privat

Kamenka Kamenka

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Article abstract of DOI:10.1016/0223-5234(94)90109-0

The racemates of cis (pip/Me) 1-[1-(2-thienyl)-2-methylcyclohexyl]piperidine and cis (pip/Me) 1-[1-(2-furanyl)-2-methylcyclohexyl]piperidine, 2 derivatives of the noncompetitive N-methyl-D-aspartate (NMDA) antagonist 1-[1-(2-thienyl)cyclohexyllpiperidine

Full text of DOI:10.1016/0223-5234(94)90109-0

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Product name:1-(RS)-(2-furanyl)-2-(RS)-methylcyclohexan-1-ol

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