Arylpyrrolidine derivatives as NK-1 /SSRI antagonists

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C514S413000, C514S422000, C548S518000, C548S469000, C548S560000, C548S577000

Reexamination Certificate

active

07138423

ABSTRACT:
The present disclosure relates to chemical compounds and their use in treatment of human diseases. A particular embodiment relates to compounds of Formula (I) or an isomer, a pharmaceutically acceptable salts or solvates thereof or a pharmaceutically acceptable formulation comprising said compoundsare useful for the treatment or prevention of conditions mediated by tachykinins and/or selective inhibition of serotonin reuptake transporter protein. The compounds act as dual NK-1 antagonists and selective serotonin reuptake inhibitors.

REFERENCES:
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patent: WO 2004/005255 (2004-01-01), None
patent: WO 2004/005256 (2004-01-01), None
Kramer et al. (1998), Science, 281, 1640.
Maggi (1995), vol. 26, No. 5, P911 (Abstract).
Kramer, Mark S., et al., “Distinct Mechanism for Antidepressant Activity by Blockade of Central Substance P Receptors”,Science, 281 (1998) 1640-1645.
Maubach, Karen A., et al., “Novel Strategies for Pharmacotherapy of Depression”,Current Opinion in Chemical Biology, 3 (1999) 481-488.
Rosen, Terry J., et al., “Synthesis and Structure-Activity Relationships of CP-122,721, A Second-Generation NK-1 Receptor Antagonist”, ,Bioorganic&Medicinal Chemistry Letters, 8 (1998) 281-284.
Ryckmans, Thomas, et al., “First Dual NK1Antagonists-Serotonin Reuptake Inhibitors: Synthesis and SAR of a New Class of Potential Antidepressants”,Bioorganic&Medicinal Chemistry Letters, 12 (2002) 261-264.

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