Oxyalkyne compounds, pharmaceutical compositions containing them

Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acid esters

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560221, 560223, 560225, 560250, 560251, 560255, 549 29, 549 74, 549 75, 549 76, 549 77, 546339, 546340, 546346, 574438, 574311, 574337, 574443, C07C 6700, A61K 3138, C07D30752

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active

053269020

ABSTRACT:
Oxyalkyne compounds corresponding to the formula I ##STR1## in which the substituent Y in the meta- or para-position is R.sup.1 represents CH.sub.3 or NH.sub.2, R.sup.2 represents H or CH.sub.3, R.sup.3 represents H, C.sub.1-3 -alkyl or COCH.sub.3, and Ar represents an aromatic residue selected from the group ##STR2## with the proviso that the substituents R.sup.4, R.sup.5 and R.sup.6 are the same or different and each substituent represents H, F, Cl, Br, C.sub.1-6 -alkyl, CF.sub.3 or C.sub.1-6 -alkoxy, and R.sup.7 represents H, F, Cl, Br, C.sub.1-3 -alkyl or CF.sub.3,
in the form of their racemates or mixtures of diastereoisomers or in optically active form, which are suitable active ingredients in pharmaceutical compositions.

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Tateson et al., "Selective Inhibition of Arachidonate 5-Lipoxygenase by Novel Acetohydroxamic Acids: Biochemical Assessment in vitro and ex vivo", Brit. J. Pharacol., vol. 94, pp. 528-539 (1988).
Pratt et al., "Oxidation by Solids. I. Oxidation of Selected Alcohols by Manganese Dioxide", J. Organic. Chem., vol. 26, pp. 2973-2975 (1961).
Corey et al., "Useful Procedures for the Oxidation of Alcohols Involving Pyridinium Dichromate in Aprotic Media", Tetrahedron Lett., No. 5, pp. 399-402 (1979).

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