Indole derivatives

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

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514253, 514323, 514414, 5142352, 540602, 544143, 544373, 546201, 548467, A61K 31445, A61K 31495, C07D40112, C07D40312

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active

055654479

ABSTRACT:
A compound of formula (I) ##STR1## wherein R.sup.1 and R.sup.2 each represents a hydrogen atom or an alkyl group, Z represents a ring selected from: ##STR2## in which n represents 4, 5 or 6; ##STR3## in which R.sup.3 represents hydrogen or an alkyl group and R.sup.4 represents an alkyl, methoxy benzyl or R.sup.5 NHCO group, R.sup.5 being an alkyl group; and ##STR4## in which R.sup.6 represents an alkyl group. and pharmaceutically acceptable salts thereof are useful in the treatment of migraine and other conditions. They are prepares by decarboxylation of the corresponding indolyl 2-carboxylic acid.

REFERENCES:
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Howell, B. A., "A Convenient Method for the Preparation of 2,4-Dinitrophenylhydrazones," Journal of Chemical Education, p. 176 (1984).
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Humphrey, P. P. A. et al., "GR43175, a selective agonist for the 5-HT.sub.1 -like receptor in dog isolated saphenous vein," Br. J. Pharmacol., vol. 94, pp. 1123-1132, (1988).
Bruinvels, A. T., et al., "5-HT.sub.1D binding sites in various species: similar pharmacological profile in dog, monkey, calf, guinea-pig and human brain membranes", Naunyn-Schmiedeberg's Arch Pharmacol, vol. 346, pp. 243-248 (1992).
Gozlan, H. et al., "Identification of presynaptic serotonin autoreceptors using a new ligand: .sup.3 H-PAT," Nature, vol. 305, pp. 140-143 (Sep. 8, 1983).
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