Morinidazole
CAS No. 92478-27-8
Morinidazole ( —— )
产品货号. M26305 CAS No. 92478-27-8
吗啉硝唑表现出抗菌活性,可用于厌氧菌引起的阑尾炎、盆腔炎等细菌感染研究。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥107 | 有现货 |
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| 5MG | ¥155 | 有现货 |
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| 10MG | ¥263 | 有现货 |
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| 500MG | 获取报价 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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| 1 mL x 10 mM in DMSO | ¥170 | 有现货 |
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生物学信息
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产品名称Morinidazole
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述吗啉硝唑表现出抗菌活性,可用于厌氧菌引起的阑尾炎、盆腔炎等细菌感染研究。
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产品描述Morinidazole shows antibacterial activity and can be used in studies about bacterial infections research such as appendicitis and pelvic inflammatory disease caused by anaerobic bacteria.(In Vitro):Morinidazole shows antibacterial activity against Trichomonas vaginalis and Entamoeba histolytica with MICs of 2 and 3 μg/mL.(In Vivo):Morinidazole (20 and 25 mg/kg; p.o.) inhibits Trichomonas vaginalis and Entamoeba histolytica in vivo. In the renal failure model in SD rats, Morinidazole (50 mg/kg; i.v.) shows a higher concentration in the liver, plasma, and kidney than lung, spleen, and heart.
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体外实验Morinidazole can be metabolized to N+-glucuronide of S-morinidazole [M8-1] and N+-glucuronide of R-morinidazole [M8-2] via N+-glucuronidation, and sulfate conjugate of morinidazole [M7] via sulfation.M7 is a substrate for organic anion transporter 1 (OAT1) and OAT3 (Km=28.6 and 54.0 μM, respectively), M8-1 and M8-2 are the substrates for OAT3.Morinidazole shows activity against Trichomonas vaginalis and Entamoeba histolytica in vitro, with MIC values of 2 μg/mL and 3 μg/mL, respectively.
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体内实验Morinidazole (20 mg/kg or 25 mg/kg; p.o.; single dose) inhibits Trichomonas vaginalis and Entamoeba histolytica in vivo in rats with EC50s of 20 mg/kg and 25 mg/kg, respectively.Morinidazole (50 mg/kg; i.v.; 0.25, 0.75, 1.5 h) shows a different concentration in tissues after intravenous injection, with a higher concentration in liver, kidney, plasma than lung, heart, and spleen in mice.Pharmacokinetic parameters of Morinidazole in control and 5/6 nephrectomized (Nx) rats.Intravenous injection; 50 mg/kg Morinidazole; Blood samples were collected from retro-orbital venous plexus before the dose (0 hours), at 5, 15, and 30 minutes, and at 1, 2, 4, 6, 8, and 12 hours after the dose. Animal Model:Renal failure model in SD rats (180-220 g)Dosage:50 mg/kg Administration:Intravenous injection; sacrificed rats at 0.25, 0.75, and 1.50 hours after dose administration Result:Increased plasma exposures slightly compared with control.
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同义词——
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通路GPCR/G Protein
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靶点Antibacterial
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受体——
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研究领域——
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适应症——
化学信息
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CAS Number92478-27-8
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分子量270.289
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分子式C11H18N4O4
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : ≥ 100 mg/mL (369.97 mM)
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SMILESCc1ncc(n1CC(O)CN1CCOCC1)[N+]([O-])=O
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1.Jiang Y, Liu FJ, Wang YM, Li HJ. Dereplication-guided isolation of novel hepatoprotective triterpenoid saponins from Celosiae Semen by high-performance liquid chromatography coupled with electrospray ionization tandem quadrupole-time-of-flight mass spectrometry. J Pharm Biomed Anal. 2017 Jan 5;132:148-155.
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