Pyributicarb
CAS No. 88678-67-5
Pyributicarb ( TSH-888 )
产品货号. M20997 CAS No. 88678-67-5
Pyributicarb 是 CYP3A4 基因和人孕烷 X 受体 (hPXR) 的有效激活剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 25MG | ¥389 | 有现货 |
|
| 50MG | ¥583 | 有现货 |
|
| 100MG | ¥851 | 有现货 |
|
| 200MG | ¥1256 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称Pyributicarb
-
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
-
产品简述Pyributicarb 是 CYP3A4 基因和人孕烷 X 受体 (hPXR) 的有效激活剂。
-
产品描述Pyributicarb is a potent activator of both CYP3A4 gene and human pregnane X receptor (hPXR).?
-
体外实验Pyributicarb, a carbamate-type herbicide, is a potent activator of both CYP3A4 gene and human pregnane X receptor (hPXR). Pyributicarb is found to increase the CYP3A4 reporter activity at 0.1 to 1 μM more strongly than typical CYP3A4 inducer rifampicin. Expression of hPXR-siRNA clearly diminishes the Pyributicarb-stimulated CYP3A4 reporter activity in 3-1-10 cells and decreases the endogenous CYP3A4 mRNA levels in HepG2 cells. Pyributicarb induces luciferase transcription via hPXR at low concentrations in the order of 10 nM. The relative potency of Pyributicarb for hPXR is 8.6-fold that of rifampicin (RIF).
-
体内实验Pyributicarb causes enhancement of CYP3A4-derived reporter activity in mouse livers introduced with hPXR by adenovirus.
-
同义词TSH-888
-
通路Metabolic Enzyme/Protease
-
靶点P450
-
受体CYP3A4
-
研究领域——
-
适应症——
化学信息
-
CAS Number88678-67-5
-
分子量330.44
-
分子式C18H22N2O2S
-
纯度>98% (HPLC)
-
溶解度DMSO:100 mg/mL (302.63 mM)
-
SMILESCOc1cccc(N(C)C(=S)Oc2cccc(C(C)(C)C)c2)n1
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Matsubara T Noracharttiyapot W Toriyabe T et al. Assessment of Human Pregnane X Receptor Involvement in Pesticide-Mediated Activation of CYP3A4 Gene[J]. Drug Metabolism and Disposition 2007 35(5):728-733.
产品手册
关联产品
-
Ambroxol
Ambroxol (NA-872) 是前体溴己辛的活性代谢产物,具有强效祛痰作用。Ambroxol 是一种葡糖脑苷脂酶 (GCase) 伴侣,可增加葡糖脑苷脂酶的活性。Ambroxol 可诱导肺自噬,并有用于帕金森氏病和神经性戈谢病研究的潜力。
-
NSC 207895
NSC 207895 抑制 MDMX,IC50 为 2.5 μM,从而增强 p53 稳定性/激活和 DNA 损伤,并调节 MDM2(一种 E3 连接酶)。
-
Vorozole
Vorozole 是一种有效的,选择性的,具有口服活性的非甾体 芳香酶 抑制剂。Vorozole 表现出体内抗肿瘤作用。Vorozole 具有研究乳腺癌的潜力。
021-51111890
购物车()
sales@molnova.cn

