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| Item type: | Article | ||||
|---|---|---|---|---|---|
| Journal or Publication Title: | Arzneimittel-Forschung = Drug research | ||||
| Publisher: | Editio-Cantor-Verlag | ||||
| Volume: | 12 | ||||
| Page Range: | pp. 1162-1166 | ||||
| Date: | 1962 | ||||
| Additional Information (public): | 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) | ||||
| Institutions: | Chemistry and Pharmacy > Institute of Pharmacy > Alumni or Retired Professors > Prof. Schönenberger | ||||
| Identification Number: |
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| Keywords: | Nerves (anesthetic effect on) Fungicides or Fungistats (hydroxyaryl amides as) | ||||
| Dewey Decimal Classification: | 500 Science > 540 Chemistry & allied sciences | ||||
| Status: | Published | ||||
| Refereed: | Yes, this version has been refereed | ||||
| Created at the University of Regensburg: | Unknown | ||||
| Item ID: | 18164 |
Abstract
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 ...
Abstract
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.
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