Synthesis and anthelmintic activity of 4-alkoxy-1-naphthamidines.
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Amidines↗
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Results for “ANTHELMINTICS”
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Novel anthelmintic agents. IV. Noncyclic amidines related to pyrantel.
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Amidines↗
Novel anthelmintic agents. V. Thiazoline and dihydrothiazine analogs of pyrantel.
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Ancylostoma↗
Anthelmintic quaternary salts. V. 2-(p-dialkylaminophenyl)-1-methylquinolinium salts.
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Animals↗
2-(Substituted amino)quinolizinium bromides. A new class of anthelmintic agents.
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Animals↗
Anthelmintic quaternary salts. 3. Benzothiazolium salts.
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Alkylation↗
The activity of phenothiazine anthelmintics as related to semiquinone formation.
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Animals↗
Possible anthelmintic thiazol-5-ylbenzimidazoles. 3.
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Anthelmintics↗
Imidoylureas. A new class of anthelmintics.
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Animals↗
Anthelmintic quaternary salts. IV. Amino-pentadienylidene-ammonium salts.
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Animals↗
Antiamebic, antimalarial, and anthelmintic effects of distal hydrazine analogs of azacrine, quinacrine, and 7-([3-(octylamino)propyl]amino)benz[c]acridine.
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Acridines↗
Novel anthelmintic agents. II. Pyrantel and other cyclic amidines.
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Amidines↗
Novel anthelmintic agents. 3. 1-(2-Arylvinyl)pyridinium salts.
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Animals↗
Anthelmintic quaternary salts. Thiacyanines and hemithiacyanines.
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Alkynes↗
3-Aryl-5-halomethylisoxazoles. A new class of anthelmintics.
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Animals↗
Novel broad-spectrum anthelmintics. Tetramisole and related derivatives of 6-arylimidazo[2,1-b]thiazole.
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Animals↗
Isothiourea derivatives of 6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole with broad-spectrum anthelmintic activity.
A series of isothiourea derivatives of 6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole (tetramisole) is described. The compounds are prepared by the S-alkylation of the thioureas that were obtained either by the reaction of an amine with 6-(3-isothiocyanatophenyl)-2,3,5,6-tetrahydroimidazo[2,1-b] thiazole or by the reaction of an isothiocyanate with 6-(3-aminophenyl)-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole. These derivatives have an improved spectrum of activity over tetramisole and are active against nematodes, cestodes, and trematodes. The structure-activity relationships are discussed.
Animals↗
Chemical constitution and anthelmintic activity. IV. Substituted phenothiazines.
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Anthelmintics↗