1956
DOI: 10.3382/ps.0350606
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The Anthelmintic Effect of Three Piperazine Derivatives on Ascaridia Galli (Schrank 1788)

Abstract: A CONSIDERABLE literature on the anthelmintic effects of piperazine compounds has accumulated. Since this has been reviewed in several recent papers mention is only made of publications which have a direct bearing on the subject of the present paper. Guilhon (1951) discussed the activity of piperazine against Ascaridia columbae and Capillaria columbae in pigeons. Sloan, Kingsbury and Jolly (1954) were the first British workers to report results obtained with some forty piperazine compounds. These authors descr… Show more

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Cited by 18 publications
(6 citation statements)
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“…Indeed, different substitutions lead to different biological activities in the piperazine substituted molecules. Piperazines were previously described to be applied as antihistaminic, anthelmintic, antidepressants, among others applications. , …”
Section: Pharmacology Of Bucinnazinementioning
confidence: 99%
“…Indeed, different substitutions lead to different biological activities in the piperazine substituted molecules. Piperazines were previously described to be applied as antihistaminic, anthelmintic, antidepressants, among others applications. , …”
Section: Pharmacology Of Bucinnazinementioning
confidence: 99%
“…Against adult ascarids the therapeutic dose of PIP (100 mg/kg) is 4-fold higher than that of LEV (28 mg/kg) and up to 20-fold higher than that of BZ anthelmintics such as FBZ (5–10 mg/kg). However, PIP has been shown to have poor efficacy against immature A. galli (Leiper, 1954; Horton-Smith & Long, 1956; Alicata, 1958; Feyera et al , 2021b, et al , 2022) and this appears to extend to freshly hatched larvae in the LMIA as the likely reason for the very much higher EC 50 values observed for this anthelmintic. In summary, the current study showed that the LMIA, using artificially hatched A. galli larvae, could potentially be used for anthelmintic sensitivity studies against A. galli .…”
Section: Discussionmentioning
confidence: 99%
“…Among these are nicotine sulfate, Bleeker (1933), Levine (1938); carbon tetrachloride, Ackert and Graham (1935); phenothiazine and nicotine-bentonite, Guthrie and Harwood (1942), Harwood and Guthrie (1944), Jaquette and Wehr (1949); piperazine and its derivatives, Olivier and Hardcastle (1943), Sloan et al (1954), Shumard and Eveleth (1955), Bradley (1955), Horton-Smith and Long (1956), Reid (1957), and Edgar et al (1957); and antibiotics, Todd (1951), Hansen et al (1953), Shumard et al (1958), Frazier (1959), Dixon et al (1959), Foster et al (1960) and Latif (1960).…”
Section: Introductionmentioning
confidence: 99%