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antiemetic/upala

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Synthetic endogenous cannabinoids analogues and uses thereof

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STATEMENT OF THE INVENTION The present invention relates to compounds of the general formula (I), to a process for their preparation, to pharmaceutical compositions containing at least one compound of the invention and to the different uses of said compounds. BACKGROUND OF THE INVENTION Anandamide
This application is a 371 of PCT/U.S.92/07718, filed Sep. 11, 1992. FIELD OF THE INVENTION The present invention relates to (3S,4S)-delta-6-tetrahydrocannabinol-7-oic acids and homologs and derivatives thereof, essentially free of the (3R,4R) form, and to processes for their preparation. The

Substituted C-furan-2-yl-methylamine and C-thiophen-2-yl-methylamine compounds

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FIELD OF THE INVENTION The present invention relates to substituted C-furan-2-yl-methylamine and C-thiophen-2-yl-methylamine compounds to a process for their preparation, to medicaments and pharmaceutical compositions containing them, and to their use in methods of treatment and in the preparation

Substituted C-furan-2-yl-methylamine and C-thiophen-2-yl-methylamine compounds

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FIELD OF THE INVENTION The present invention relates to substituted C-furan-2-yl-methylamine and C-thiophen-2-yl-methylamine compounds to a process for their preparation, to medicaments and pharmaceutical compositions containing them, and to their use in methods of treatment and in the preparation

Tachykinin (NK1) receptor antagonists

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BACKGROUND OF THE INVENTION Over the last decade, major advances have been made in the understanding of the biology of the mammalian tachykinin neuropeptides. It is now well established that substance-P (1), neurokinin A (NKA) (2), and neurokinin B (NKB) (3), all of which share a common C-terminal

Substituted alkyltetraamine derivatives

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FIELD OF THE INVENTION The present invention relates to substituted alkyltetraamine derivatives which are useful as a tachykinin antagonist. BACKGROUND OF THE INVENTION Tachykinin is a general term for a group of peptides having similar structures. Substance P (SP), neurokinin A (NKA) and neurokinin

Topical anesthetic formulation

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FIELD OF THE INVENTION The present invention generally relates to transdermal medicaments, and in particular to a fast acting transdermal medicament delivery for penetration through the stratum corneum into the deep epidermis/dermis and is especially well suited for local anesthesia. BACKGROUND OF
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