Triclosan
| 规格 | 价格 | 货期 | 数量 |
|---|---|---|---|
| 1mL(10 mM in DMSO) | ¥454.00 | 现货 | |
| 1g | ¥567.00 | 现货 | |
| 5g | ¥1772.00 | 现货 |
特色产品
- 用于免疫印迹和质谱分析等后续操作
- 适用于30 KDa-130 KDa大小的蛋白
- 可将信号灵敏度提高100倍
- 同时保持稳定的特异性和分辨率
- 提供更高的转录效率并抑制免疫激活
- 使用5-moUTP和Cy5-utp修饰
产品描述
Triclosan is a synthetic, lipid soluble broad-spectrum antibacterial and antifungal agent which is widely used in personal care products, household items, medical devices, and fabrics and plastics. It, distributed ubiquitously across the ecosystem, possesses intrinsic oestrogenic and androgenic activity which could provide some explanation for the endocrine disrupting properties described in aquatic species.
In vitro: Triclosan blocked and displaced [3H] oestradiol binding from oestrogen receptors (ER) of MCF7 human breast cancer cells and from recombinant human ERα /ERβ at low concentrations. Triclosan fully dampened the elicitation of the oestrogen-responsive ERE-CAT reporter gene in MCF7 cells and the activation of growth of MCF7 human breast cancer cells by 10-10 M 17β-oestradiol. Additionally, Triclosan, on its own, increased the proliferation of oestrogen-dependent MCF7 human breast cancer cells [1].
In vivo: BALB/c mice were administrated subcutaneously with triclosan daily at 0.8 to 38 mg/kg for 6 weeks. 75% parasitemia was blocked by single subcutaneous injection of triclosan at a dose of 3.0 mg/kg within 24 hours. However, triclosan fully cleared the parasite from circulation with one injection at a dose of 38 mg/kg. No side effects of triclosan were monitored via checking the activities of the enzymes serum glutamate oxaloacetate transaminase and serum glutamate pyruvate transaminase [2].
References:
[1]. Gee, R., Charles, A., Taylor, N., & Darbre, P. Oestrogenic and androgenic activity of triclosan in breast cancer cells. Journal of Applied Toxicology. 2007; 28(1): 78-91.
[2]. Hillyer, C. Triclosan offers protection against blood stages of malaria by inhibiting enoyl-ACP reductase of Plasmodium falciparumM. Surolia, A. Surolia. Nat Med 7:167–173, 2001. Transfusion Medicine Reviews. 2002; 16(2): 180-181.
产品性质
| 物理外观 | Solid |
| CAS号 | 3380-34-5 |
| 分子式 | C12H7Cl3O2 |
| 分子量 | 289.5 |
| 化学名称 | 5-chloro-2-(2,4-dichlorophenoxy)-phenol |
| 溶解度 | insoluble in H2O; ≥10.95 mg/mL in DMSO; ≥47.7 mg/mL in EtOH |
| SMILES | Oc(cc(cc1)Cl)c1Oc(ccc(Cl)c1)c1Cl |
| 存储条件 | 室温 |
| 运输条件 | 蓝冰 |
产品应用 (实验数据来自文献,APExBIO并未验证,仅供参考)
IC50和靶点
| 生物活性描述 | 三氯生是一种广谱抗菌剂,可在烯酰-酰基载体蛋白还原酶(FabI)步骤中抑制细菌脂肪酸的合成。三氯生能抑制大肠杆菌烯酰-酰基载体蛋白还原酶(FabI)和在第 93 位含有甘氨酸-缬氨酸置换的 FabI(FabIG93V),其 IC50 分别为 2 μM 和 10 μM。三氯生会导致培养的大鼠神经干细胞(NSC)凋亡。在动物模型中,三氯生会加剧结肠炎和结肠炎相关的结肠直肠肿瘤发生。 |



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