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Oxfendazole 99%

Oxfendazole

源葉(MedMol)
S81489
53716-50-0
C15H13N3O3S
315.35
品牌 貨號 產品規格 價格(RMB) 庫存(上海) 北京 武漢 南京 購買數量
源葉(MedMol) S81489-100mg 99% ¥120.00元 3 - - -
源葉(MedMol) S81489-500mg 99% ¥224.00元 6 - - -
產品介紹 參考文獻 質檢證書(COA) 摩爾濃度計算器 相關產品

產品介紹

Oxfendazole, a broad spectrum benzimidazole anthelmintic, protects livestock against roundworm, strongyles and pinworms.
產品描述: Oxfendazole, a broad spectrum benzimidazole anthelmintic, protects livestock against roundworm, strongyles and pinworms.
靶點: Glucokinase;Microtubule Associated;Parasite;Glucokinase;?MicrotubuleAssociated;?Parasite
體內研究:
Oxfendazole (OX) induces not only mRNA expression of phase I enzymes Cyp1a1, Cyp1a2, but also Nrf2-regulated phase II enzymes such as Gpx2, Nqo1, Yc2, Akr7a3 and Gstm1 in rats, presumably due to an adaptive response against OX-induced oxidative stress. Oxfendazole enhances oxidative DNA damage (as assessed by 8-hydroxydeoxyguanosine; 8-OHdG) and lipid peroxidation (as assessed by thiobarbituric acid-reactive substances; TBARS) in rats. Oxfendazole administered at the therapeutic dose (4.5 mg/kg) and at the highest dose (22.5 mg/kg) increase 1.54- and 2.36-fold the total liver microsomal cytochrome P450 and more particularly the isoenzyme P450IA2 (95% and 184% increases) in rabbit liver. Oxfendazole MRL induces a mutagenic effect in all tested cell types. Oxfendazole exhibits embryotoxicity including teratogenicity. Oxfendazole induces a disturbance in the different biochemical contents of all tested tissues in mice. Oxfendazole increases the incidence and multiplicity of altered foci (4.0- and 3.6-fold, respectively) and hepatocellular adenomas (HCAs) (3.0- and 5.5-fold, respectively). Oxfendazole treatment induces 5.2- and 5.6-fold increases in the number of proliferating cell nuclear antigen (PCNA)-positive cells and single-stranded DNA (ssDNA)-positive cells in HCAs compared with the surrounding tissue, respectively. Oxfendazole and its sulphone metabolite attain a significantly higher plasma concentration and remain much longer in plasma compared with fenbendazole (FBZ) and albendazole (ABZ) and
參考文獻:
1.Dewa Y, et al. Arch Toxicol,2009, 83(5), 503-511. 2.Dewa Y, et al. Arch Toxicol,2011, 85(2), 155-162. 3.El-Makawy A, et al. Reprod Nutr Dev,2006, 46(2), 139-156. 4.Gokbulut C, et al. Vet Parasitol,2007, 148(3-4), 279-287. 5.Gleizes C, et al. Biochem Pharmacol,1991, 41(12), 1813-1820.
溶解性: Ethanol:<1  mg/mL    H2O:<1  mg/mL    DMSO:10  mg/mL  (31.71  mM)
保存條件: 2-8℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 3.171 ml 15.855 ml 31.711 ml
5 mM 0.634 ml 3.171 ml 6.342 ml
10 mM 0.317 ml 1.586 ml 3.171 ml
50 mM 0.063 ml 0.317 ml 0.634 ml
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參考文獻

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