Results 221 to 230 of about 7,383 (256)

Salinomycin

Reactions Weekly, 2022
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Salinomycin poisoning in turkeys

Veterinary Record, 1984
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Tiamulin/salinomycin interactions in pigs

Veterinary Record, 1986
D J, Miller, J J, O'Connor, N L, Roberts
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Salinomycin poisoning in veal calves

Veterinary Record, 2001
M W, Huyben, J, Sol, G H, Counotte, M P, Roumen, G H, Borst   +4 more
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[Effect of salinomycin on lambs for fattening].

Veterinarno-meditsinski nauki, 1982
When applied to male Trakiiska tunkorounna lambs of initial weight 18.6 kg in the course of 90 days at concentrations of 6 g, 12 g, and 24 g per ton of forage slinomycin brought about a rise of liveweight and average weight gain in the treated animals (for the weight gain 12.2, 16.7, and 19.4 per cent, respectively, as against the controls).
D, Drumev, V, Rusev, A, Petkov, E, Enev, D, Pashov   +4 more
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Accidental salinomycin intoxication in calves.

The Canadian veterinary journal = La revue veterinaire canadienne, 2011
Twenty-four 10- to 16-week-old calves in a dairy herd in Birjand, Iran, inadvertently received an excessive dose of salinomycin mixed with barley grain. There was 58% mortality within 10 d. The calves had high serum AST, LDH, and CK activities; histopathologic lesions in myocardium, liver, and kidneys; and clinical signs associated with acute and ...
Arash, Omidi, Mohammad R, Aslani, Ahmad R, Movassaghi, Mehrdad, Mohri, Mohammad, Dadfar   +4 more
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The synergistic anticancer effect of salinomycin combined with cabazitaxel in CD44+ prostate cancer cells by downregulating wnt, NF-κB and AKT signaling

Molecular Biology Reports, 2022
S. Erdogan, R. Serttaş, K. Turkekul, I. Dibirdik   +3 more
semanticscholar   +1 more source

Salinomycin

Cold Spring Harbor Protocols, 2008
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Hesperidin/Salinomycin Combination; a Natural Product for Deactivation of the PI3K/Akt Signaling Pathway and Anti-Apoptotic Factors in KG1a Cells

Journal of Fluorescence
Sina Abroon, Mohammad Nouri, Majid Mahdavi   +2 more
semanticscholar   +1 more source

Salinomycin : the bis-spiroacetal moiety [PDF]

, 1985
The synthesis of (Z)-7,8-epoxy-7-methyl-1-(tetrahydro-2-methoxypyran-2-yl)-1-octen-4-one (87) and 7,8-epoxy-7-methyl-1-(tetrahydro-2-methoxy- pyran-2-yl)-octan-4-one (115) are described. In both cases, the key step was the addition of the lithium acetylide prepared from 7-methyl-4- trimethylsilyloxy-7-octen-1-yne (98) to δ-valerolactone (97).
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