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1、Hotline: 400-820-3792Inhibitors Agonists Screening Librarieswww.MedChemERifampicinCat. No.: HY-B0272CAS No.: 13292-46-1Synonyms: Rifampin; Rifamycin AMP分式: CHNO分量: 822.94作靶点: Bacterial作通路: Anti-infection储存式: Powder -20C 3 years4C 2 yearsIn solvent -80C 6 months-20C 1 month溶解性数据体外实验 DMSO : 50 mg/mL (
2、60.76 mM; Need ultrasonic)H2O : 40% PEG300 5% Tween-80 45% salineSolubility: 2.5 mg/mL (3.04 mM); Clear solution; Need ultrasonic2. 请依序添加每种溶剂: 10% DMSO 90% (20% SBE-CD in saline)Solubility: 2.5 mg/mL (3.04 mM); Clear solution1/3 Master of Small Molecules 您边的抑制剂师www.MedChemEBIOLOGICAL ACTIVITY物活性 Rif
3、ampicin种有效的谱抗素,可抵抗细菌病原体。体外研究 Rifampicin (100 mg/mL) can block the functional activity of P-glycoprotein. Rifampicin is not a substract for P-glycoprotein. The mechanism of rifampicin resistance is unassociated with the functional activity of P-glycoprotein 3.体内研究 Rifampicin (200, 400 mg/kg) can indu
4、ce fatty liver at high concentration 1. Rifampicin (30 mg/kg, i.p.)treatment of S464P biofilms in vivo results in a slight decline, but earlier rebinds in bioluminescence fromthese catheters compared with the parental signal, whereas rifampicin has no affect on bioluminescence inmice infected with m
5、utant H481Y 2.PROTOCOLAnimal Briefly, 1 cm Teflon catheter (14-gauge) carrying 104 cfu S. aureus, either the parental strain Xen 29 or theAdministration 2 RifR mutants S464P or H481Y, are implanted subcutaneously in groups of nine mice per strain. One cathetersegment is inserted on each side of each
6、 animal. Six days after the implantation of the catheters, five micefrom each group are treated with rifampicin at 30 mg/kg intraperitoneally in 0.1 mL saline, twice daily for fourconsecutive days. The remaining four mice in each group are left untreated as controls. At various timepoints during the
7、 infection, the mice are anaesthetized using a constant flow of 1.5% isoflurane from theIVIS manifold, and imaged using an IVIS Image System 100 Series. The bioluminescent signals(photons/s) emitted from the mice are analysed using LivingImage software and plotted over the course ofinfection. The mi
8、ce are sacrificed 20 days after infection (11 days after final rifampicin treatment). Thecatheters are surgically removed and the bacteria are detached by sonication for determination of bacterialburdens on the catheters.MCE has not independently confirmed the accuracy of these methods. They are for
9、 reference only.户使本产品发表的科研献 Phytomedicine. 2019 Mar 15;56:175-182. RSC Adv. 2019 May. Onco Targets Ther. 2018 Sep 17;11:5885-5894. Xenobiotica. 2019 Feb 11:1-33.See more customer validations on HYPERLINK / www.MedChemEREFERENCES1. Piriou A, et al. Fatty liver induced by high doses of rifampicin in t
10、he rat: possible relation with an inhibition of RNA polymerases ineukariotic cells. Arch Toxicol Suppl. 1979;(2):333-7.2. Yu J, et al. Monitoring in vivo fitness of rifampicin-resistant Staphylococcus aureus mutants in a mouse biofilm infection model. J2/3 Master of Small Molecules 您边的抑制剂师www.MedChemEAntimicrob Chemother. 2005 Apr;55(4):528-34. Epub 2005 Mar 2.3. Erokhina MV, et al. In vitro development of rifampicin resistance in the epithelial cells. Probl Tuberk Bolezn Legk. 2006;(8):58-61.McePdfHeightCaution: Product has not been
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