β-Glucuronidase-IN-1
CAS No. 484006-66-8
β-Glucuronidase-IN-1 ( —— )
产品货号. M33191 CAS No. 484006-66-8
β-Glucuronidase-IN-1 是强效的,选择性,非竞争性和具有口服活性的 E. coli β-葡萄糖醛酸酶 (β-glucuronidase) 抑制剂,针对 E. coli β-葡萄糖醛酸酶的 IC50 和 Ki 值分别为 283 nM 和 164 nM。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 2MG | ¥491 | 有现货 |
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| 5MG | ¥719 | 有现货 |
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| 10MG | ¥1122 | 有现货 |
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| 25MG | ¥1822 | 有现货 |
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| 50MG | ¥2714 | 有现货 |
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| 100MG | ¥3947 | 有现货 |
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| 500MG | ¥8339 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
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产品名称β-Glucuronidase-IN-1
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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β-Glucuronidase-IN-1 是强效的,选择性,非竞争性和具有口服活性的 E. coli β-葡萄糖醛酸酶 (β-glucuronidase) 抑制剂,针对 E. coli β-葡萄糖醛酸酶的 IC50 和 Ki 值分别为 283 nM 和 164 nM。
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产品描述β-Glucuronidase-IN-1 is a potent, selective, uncompetitive, and orally active E. coli bacterial β-glucuronidase inhibitor, exhibitingan IC50 and a Ki of 283 nM and 164 nM, respectively.
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体外实验β-Glucuronidase-IN-1 (Inhibitor 1) (0.01-100 μM) inhibits E. coli?β-glucuronidase activity as a dose-dependent manner and exhibits an IC50 and a Ki value with 283 nM and 164 nM, respectively.β-Glucuronidase-IN-1 (100 μM; 24-72 hours) maintains potent efficacy in living bacterial cells (EC50=17.7 nM), it does not affect bacterial cell growth under aerobic or anaerobic conditions or killing mammalian epithelial cells. Cell Viability AssayCell Line:CMT93, CaCO-2, HCT116 cells Concentration:100 μM Incubation Time:24hours, 48 hours and 72 hours Result:Did not impact mammalian cell survival and any reduction in cell viability were attributed to the presence of DMSO.
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体内实验β-Glucuronidase-IN-1 (oral gavage; 10 μg; twice per day; 11 days) protects the mouse GI epithelium from CPT-11–induced damage and protects the glandular structure of CPT-11-treated intestinal tissues.Animal Model:Healthy 6- to 8-week-old Balb/cJ mice Dosage:10 μg Administration:Oral gavage; twice per day; 11 daysResult:Alleviated CPT-11-induced toxicity in mice.
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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Antibacterial
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研究领域——
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适应症——
化学信息
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CAS Number484006-66-8
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分子量425.54
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分子式C23H27N3O3S
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO 中的溶解度 : 100 mg/mL (235.00 mM; 超声助溶 (<60°C)
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SMILESCCOc1ccc(NC(=S)N(CCO)Cc2cc3cc(C)cc(C)c3[nH]c2=O)cc1
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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. Wallace BD, et al. Alleviating cancer drug toxicity by inhibiting a bacterial enzyme.Science.?2010 Nov 5;330(6005):831-5.?
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