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Clindamycin hydrochloride monohydrate(Clindamycin alcoholate)是一种口服蛋白质合成抑制剂,具有在金黄色葡萄球菌中以亚抑制浓度(sub-MICs)抑制毒力因子表达的能力。其抗性来源于50S核糖体亚基(23S rRNA)的抗生素结合位点通过酶促甲基化。此外,Clindamycin hydrochloride monohydrate能显著减少杀白细胞毒素(PVL)、毒性休克-葡萄球菌毒素(TSST-1)或α-溶血素(Hla)的产生。

Clindamycin hydrochloride monohydrate(Clindamycin alcoholate)是一种口服蛋白质合成抑制剂,具有在金黄色葡萄球菌中以亚抑制浓度(sub-MICs)抑制毒力因子表达的能力。其抗性来源于50S核糖体亚基(23S rRNA)的抗生素结合位点通过酶促甲基化。此外,Clindamycin hydrochloride monohydrate能显著减少杀白细胞毒素(PVL)、毒性休克-葡萄球菌毒素(TSST-1)或α-溶血素(Hla)的产生。
| 规格 | 价格 | 库存 | 数量 | 
|---|---|---|---|
| 25 mg | ¥ 113  | In stock | |
| 50 mg | ¥ 155  | In stock | |
| 100 mg | ¥ 266  | In stock | |
| 200 mg | ¥ 385  | In stock | |
| 500 mg | ¥ 636  | In stock | 
Clindamycin hydrochloride monohydrate 相关产品
| 产品描述 | Clindamycin hydrochloride monohydrate (Clindamycin alcoholate) is a protein synthesis inhibitor used orally, capable of diminishing virulence factor expression in Staphylococcus aureus at sub-minimum inhibitory concentrations (sub-MICs). It acts by suppressing Panton-Valentine leucocidin (PVL), toxic-shock-staphylococcal toxin (TSST-1), and alpha-haemolysin (Hla) production. Resistance to this compound emerges through enzymatic methylation at the antibiotic's 50S ribosomal subunit binding site (23S rRNA).  | 
| 别名 | Clindamycin alcoholate | 
| 分子量 | 479.46 | 
| 分子式 | C18H36Cl2N2O6S | 
| CAS No. | 58207-19-5 | 
| Smiles | O.Cl.CCC[C@@H]1C[C@H](N(C)C1)C(=O)N[C@H]([C@H](C)Cl)[C@H]1O[C@H](SC)[C@H](O)[C@@H](O)[C@H]1O | 
| 密度 | 1.31g/cm3 | 
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 90 mg/mL (187.71 mM), Sonication is recommended.   | |||||||||||||||||||||||||||||||||||
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