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Chemical biology of salinomycin
Tetrahedron, 2018Abstract Cancer stem cells (CSC) have been shown to be refractory to conventional therapeutic agents, can promote metastasis, and have been linked to cancer relapse. The natural product Salinomycin has been identified by means of high throughput phenotypic screening as a selective killer of CSC in vitro and in vivo. In this article we comprehensively
Versini, Antoine +5 more
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Salinomycin Toxicosis in Male Breeder Turkeys
Avian Diseases, 1995A sudden outbreak of mortality in one house of 600 48-week-old male breeder turkeys on a five-house turkey breeder farm was suspected to be feed-related. The turkeys gasped and became recumbent; 21.7% of affected turkeys died. No significant gross lesions were found at necropsy.
J R, Andreasen, J H, Schleifer
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Antiproliferative activity of salinomycin and its derivatives
Bioorganic & Medicinal Chemistry Letters, 2012Antiproliferative activity of seven amides and one benzotriazole ester derivative of salinomycin, a polyether ionophore antibiotic, with recently reported antibacterial activity, are herein described. Salinomycin and the majority of derivatives exhibit potent antiproliferative activity against the drug-resistant cancer cell lines.
Adam, Huczyński +5 more
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Salinomycin activity in ruminants
1983The polyether antibiotic salinomycin (SLM), supplemented in low concentrations to the feed, showed nutritive activity in ruminants. The increase of weight gain and of feed utilization of steers was due to an increase in the percentage of propionic acid, and a decrease in the percentage of acetic acid and butyric acid in the rumen8.
D. Droumev +3 more
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Anticancer Activity of Polyether Ionophore-Salinomycin
Anti-Cancer Agents in Medicinal Chemistry, 2015Since the discovery of unusual anti-tumor activity of natural polyether antibiotic - Salinomycin, this compound, along with its derivatives, has been intensively studied against different human cancer cells, both in vivo and in vitro. Salinomycin has shown strong inhibition activity against the proliferation process of many different cancer cells ...
Michał, Antoszczak, Adam, Huczyński
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Salinomycin: A new monovalent cation ionophore
Biochemical and Biophysical Research Communications, 1975The cation discriminations of salinomycin and its derivatives have been studied by measuring complexability with cations and transport rate of them across organic phase. Salinomycin exhibited a great preference for K+ over other monovalent and divalent cations in migrating cations into organic phase in two phase systems.
M, Mitani, T, Yamanishi, Y, Miyazaki
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Salinomycin poisoning in point‐of‐lay turkeys
Australian Veterinary Journal, 1989Salinomycin poisoning occurred in a flock of 700 point‐of‐lay turkeys; 400 birds died over 7 days as a result of consuming feed contaminated with 50 ppm salinomycin. No gross lesions were detected. Histologic evidence of a myopathy was most readily detected in leg muscles of turkeys 5 to 7 d after ingesting salinomycin.
G L, Griffiths +2 more
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Salinomycin toxicity in dairy calves
Veterinary Record, 2011SINCE the beginning of October, Animal Health and Veterinary Laboratories Agency (AHVLA) regional laboratories and SAC disease surveillance centres have been investigating unusual incidents of clinical respiratory disease presentations in calves on four farms.
Andrew Holliman +3 more
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Salinomycin – A New Cancer Drug Candidate
Chemical Biology & Drug Design, 2012Very recently, it has been shown that it is possible to selectively kill breast cancer stem cells using the ionophore antibiotic, salinomycin. Its ability to kill cancer stem cells and apoptosis‐resistant cancer cells may define salinomycin as a novel anticancer drug.
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The Site of Action of the Anticoccidial Salinomycin (Coxistac)
The Journal of Parasitology, 1979The anticoccidial salinomycin has a cidal effect against chicken coccidia. Restricted and unrestricted medication studies and histopathological examinations of chicks infected with Eimeria acervulina, E. maxima, or E. tenella showed that parasites were destroyed within host cells during asexual development.
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