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53003-10-4CC[C@@H](C(=O)[C@@H](C)[C@@H](O)[C@H](C)[C@@H]1O[C@@H]([C@@H](CC)C(=O)O)CC[C@@H]1C)[C@H]1O[C@]2(C=C[C@@H](O)[C@]3(CC[C@@](C)([C@H]4CC[C@](O)(CC)[C@H](C)O4)O3)O2)[C@H](C)C[C@@H]1CKQXDHUJYNAXLNZ-XQSDOZFQSA-N53003-10-4DTXSID4048486CHEMBL1208572CHEBI:80025化学的特性solid
安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
毒性LD50 50 mg/kg(マウス,経口).
解説サリノマイシン,白色~黄色の結晶.融点112 ℃.[α]25D -63°(エタノール).pKa 6.4(DMF).λmax 284 nm(ε 126).水に不溶,有機溶媒に可溶.森北出版「化学辞典(第2版)
用途サリノマイシン,イオノホア抗生物質で,グラム陽性菌やかびに有効.ニワトリやブタが罹(り)患するコクシジウム原虫の駆除に用いられる.
説明Salinomycin was found in the culture mycelium of Streptomyces albus by Otake et al. of the University of Tokyo in 1973. Like other polyether ionophore antibiotics, it shows activity against gram-positive bacteria, fungi, and Coccidium. Salinomycin has been used as a feed additive to protect poultry against coccidial infections.
使用Salinomycin is a polyether ionophore with broad spectrum Gram positive and anti-coccidial activity. Salinomycin has a high affinity for monovalent cations, particularly potassium. Salinomycin is used to control coccidia in animals and for growth promotion in ruminants. Recently, salinomycin has been shown to inhibit cancer stem cells and is >100 times more potent than taxol. While the mechanism of action is unknown, it was noted that among the 60,000 compounds screened, another monovalent ionophore, nigericin, and a chloride channel inhibitor, avermectin, were also active.
一般的な説明Chemical structure: polyether
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