Dokumentenart: | Artikel | ||||
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Titel eines Journals oder einer Zeitschrift: | Arzneimittel-Forschung = Drug research | ||||
Verlag: | Editio-Cantor-Verlag | ||||
Band: | 12 | ||||
Seitenbereich: | S. 1162-1166 | ||||
Datum: | 1962 | ||||
Zusätzliche Informationen (Öffentlich): | CAN 59:11353 68 Pharmacodynamics 614-17-5; 6137-53-7; 14180-11-1; 14216-34-3; 90887-50-6 (Derived from data in the 7th Collective Formula Index (1962-1966); 87-17-2 (Salicylanilide); 1697-18-3 (Salicylanilide, 2'-chloro-); 2627-77-2 (Salicylanilide, 4'-bromo-); 3679-63-8 (Salicylanilide, 4'-chloro-); 13410-91-8 (Salicylanilide, 2',3'-dichloro-); 24448-71-3 (Salicylanilide, 3'-chloro-); 37183-28-1 (Salicylanilide, 2',4'-dichloro-); 106480-75-5 (Salicylanilide, 3,4'-dichloro-) (as fungicide); 55-21-0 (Benzamide); 613-93-4 (Benzamide, N-methyl-); 619-57-8 (Benzamide, p-hydroxy-); 2280-99-1 (p-Anisamide, N-butyl-); 3400-22-4 (p-Anisamide, N-methyl-); 3679-68-3 (Benzanilide, 4'-chloro-4-hydroxy-); 7403-41-0 (p-Anisamide, N-ethyl-); 7464-43-9 (p-Anisamide, N-propyl-); 7464-44-0 (p-Anisamide, N-isopropyl-); 7465-88-5 (p-Anisanilide); 7595-61-1 (p-Anisanilide, 4'-chloro-); 10546-70-0 (Benzamide, N-propyl-); 14121-97-2 (Benzanilide, 4-hydroxy-); 27519-68-2 (Benzamide, p-hydroxy-N-propyl-); 27522-79-8 (Benzamide, N-ethyl-p-hydroxy-); 27559-45-1 (Benzanilide, 3-hydroxy-); 36965-04-5 (Benzanilide, 4'-chloro-4-hydroxy-, acetate); 39114-64-2 (Benzamide, N-cyclohexyl-p-hydroxy-); 58748-19-9 (Benzamide, ethoxy-); 60696-49-3 (Benzamide, N-butyl-p-hydroxy-); 62639-20-7 (Benzanilide, 2'-chloro-4-hydroxy-); 73544-81-7 (Benzanilide, 3'-chloro-3-hydroxy-); 73544-82-8 (Benzanilide, 4'-chloro-3-hydroxy-); 79540-62-8 (Benzanilide, 2',3'-dichloro-4-hydroxy-); 83191-67-7 (Benzamide, p-hydroxy-N-isopropyl-); 92044-46-7 (Benzanilide, 2'-chloro-3-hydroxy-); 92044-47-8 (Benzanilide, 3'-chloro-4-hydroxy-); 92433-68-6 (Benzanilide, 2'-chloro-4-hydroxy-, acetate); 92433-69-7 (Benzanilide, 3'-chloro-4-hydroxy-, acetate); 92905-58-3 (Benzanilide, 4'-bromo-3-hydroxy-); 97027-63-9 (Benzanilide, 2',3'-dichloro-3-hydroxy-); 97027-64-0 (Benzanilide, 2',4'-dichloro-3-hydroxy-); 97027-65-1 (Benzanilide, 2',4'-dichloro-4-hydroxy-); 97027-66-2 (Benzanilide, 2',5'-dichloro-3-hydroxy-); 462070-14-0 (Benzanilide, 2',5'-dichloro-4-hydroxy-) (fungicidal activity of) | ||||
Institutionen: | Chemie und Pharmazie > Institut für Pharmazie > Entpflichtete oder im Ruhestand befindliche Professoren > Prof. Schönenberger | ||||
Identifikationsnummer: |
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Stichwörter / Keywords: | Nerves (anesthetic effect on) Fungicides or Fungistats (hydroxyaryl amides as) | ||||
Dewey-Dezimal-Klassifikation: | 500 Naturwissenschaften und Mathematik > 540 Chemie | ||||
Status: | Veröffentlicht | ||||
Begutachtet: | Ja, diese Version wurde begutachtet | ||||
An der Universität Regensburg entstanden: | Unbekannt / Keine Angabe | ||||
Dokumenten-ID: | 18164 |
Zusammenfassung
Among the hydroxybenzamide compds. tested, the halogenated o-, m-, and p-hydroxybenzanilides are of special importance in view of their high degree of activity. The effect is highly dependent on the position of the hydroxyl group and the halogen atoms. Optimal effects against dermatophytes were found in the compd. with the OH group in ortho position and the halogen substituted groups in 3- and ...
Zusammenfassung
Among the hydroxybenzamide compds. tested, the halogenated o-, m-, and p-hydroxybenzanilides are of special importance in view of their high degree of activity. The effect is highly dependent on the position of the hydroxyl group and the halogen atoms. Optimal effects against dermatophytes were found in the compd. with the OH group in ortho position and the halogen substituted groups in 3- and 4-position in the aniline ring. Increase of activity may be obtained by the incorporation of a 2nd halogen atom in the aniline residue.
Metadaten zuletzt geändert: 24 Mai 2018 12:20