Pexidartinib(PLX3397) 产品说明书 Chemicals
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产品编号 DC8158
名称 Pexidartinib(PLX3397)

化学性质

CAS 1029044-16-3
分子式 C20H15CLF3N5
分子量 417.81
存储条件 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

生物活性

Description
In Vivo
In Vitro

化合物的使用

Kinase Assay
Cell Assay
Animal Administration

参考文献


In the study, 23 patients with advanced PVNS in a single joint received 1000 mg of PLX3397 orally each day. Patients underwent an MRI every two months to measure tumor volume using a novel tumor volume score developed for PVNS. Among the 14 patients with evaluable MRI scans, the mean tumor size reduction was 61 percent. Eleven patients experienced a partial response (at least a 50 percent decrease in tumor volume compared to baseline screenings) and three had stable disease. Patients remained on the drug until disease progression or intolerability. For the detailed information of Pexidartinib(PLX3397), the solubility of Pexidartinib(PLX3397) in water, the solubility of Pexidartinib(PLX3397) in DMSO, the solubility of Pexidartinib(PLX3397) in PBS buffer, the animal experiment (test) of Pexidartinib(PLX3397), the cell expriment (test) of Pexidartinib(PLX3397), the in vivo, in vitro and clinical trial test of Pexidartinib(PLX3397), the EC50, IC50,and affinity,of Pexidartinib(PLX3397), For the detailed information of Pexidartinib(PLX3397), the solubility of Pexidartinib(PLX3397) in water, the solubility of Pexidartinib(PLX3397) in DMSO, the solubility of Pexidartinib(PLX3397) in PBS buffer, the animal experiment (test) of Pexidartinib(PLX3397), the cell expriment (test) of Pexidartinib(PLX3397), the in vivo, in vitro and clinical trial test of Pexidartinib(PLX3397), the EC50, IC50,and affinity,of Pexidartinib(PLX3397), Please contact DC Chemicals.
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