您好,欢迎来到易推广 请登录 免费注册

MedChemExpress 主营产品:Medchemexpress,抑制剂专家,生物试剂公司

易推广认证请放心拨打

021-58955995

当前位置: 易推广 > 生物试剂/抗体/细胞 > 生化试剂 > 其他 > MedChemExpress > 产品展示 > MCE信号通路 > MAPK/ERK 信号通路 > Sorafenib Tosylate

提示:信息由商家自行发布,信息的真伪性请消费者自己判断,信息内容的准确性由相关商家负责,易推广对此不承担任何责任。

Sorafenib Tosylate

价格:¥电议

品牌名称:$brandModel.Title(进口品牌)型号: 原产地:美洲 发布时间:2021/7/24更新时间:2024/1/2

产品摘要:Sorafenib Tosylate (Bay 43-9006 Tosylate) 是一种有效的口服活性 Raf 抑制剂,对 Raf-1 和 B-Raf 的 IC50 分别为 6 nM 和 20 nM。Sorafenib Tosylate 是一种多激酶抑制剂,对 VEGFR2,VEGFR3,PDGFRβ,FLT3 和 c-Kit 的 IC50 分别为 90 nM,15 nM,20 nM,57 nM 和 58 nM。Sorafenib Tosylate 诱导细胞自噬 (autophagy) 和凋亡 (apo

产品完善度: 访问次数:1595

企业档案

会员类型:会员

已获得易推广信誉   等级评定
171成长值

(0 -40)基础信誉积累,可浏览访问

(41-90)良好信誉积累,可接洽商谈

(91+  )优质信誉积累,可持续信赖

易推广会员:8

工商认证 【已认证】

最后认证时间:

注册号: 【已认证】

法人代表: 【已认证】

企业类型:生产商 【已认证】

注册资金:人民币万 【已认证】

产品数:91194

参观次数:10499573

手机网站:http://m.yituig.com/c131527/

旗舰版地址:http://medchemexpress.app17.com

联系我们

MedChemExpress

电话:021-58955995

联系人:客服部 (请说明是在易推广看到的!谢谢)

手机:13611715263

邮编:201203

邮箱:sales@medchemexpress.cn

地址:上海上海

详细内容

联系方式:
电话:021-58955995 手机:13611715263 联系人:客服部   Q Q:4008203792

MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务。

Sorafenib Tosylate

CAS No. : 475207-59-1

MCE 站:Sorafenib Tosylate

产品活性:Sorafenib Tosylate (Bay 43-9006 Tosylate) 是一种有效的口服活性 Raf 抑制剂,对 Raf-1B-RafIC50 分别为 6 nM 和 20 nM。Sorafenib Tosylate 是一种多激酶抑制剂,对 VEGFR2VEGFR3PDGFRβFLT3c-KitIC50 分别为 90 nM,15 nM,20 nM,57 nM 和 58 nM。Sorafenib Tosylate 诱导细胞自噬 (autophagy) 和凋亡 (apoptosis),并具有抗肿瘤活性。Sorafenib Tosylate 也是一种 ferroptosis 激动剂。

研究领域:MAPK/ERK Pathway  |  Protein Tyrosine Kinase/RTK  |  Autophagy  |  Apoptosis

作用靶点:Raf  |  VEGFR  |  FLT3  |  Autophagy  |  Ferroptosis  |  Apoptosis

In Vitro: Sorafenib Tosylate also inhibits BRAFwt (IC50=22 nM), BRAFV599E (IC50=38 nM), VEGFR-2 (IC50=90 nM), VEGFR-3 (IC50=20 nM), PDGFR-β (IC50=57 nM), c-KIT (IC50=68 nM), and Flt3 (IC50=58 nM) in biochemical assays. Sorafenib-induced phosphorylation of c-Met, p70S6K and 4EBP1 is significantly reduced when 10-0505 cells are co-treated with anti-human anti-HGF antibody, suggesting that treatment with Sorafenib Tosylate leads to increased HGF secretion and activation of c-Met and mTOR targets.

In Vivo: Sorafenib Tosylate (10, 30, 50 and 100 mg/kg, orally) treatment inhibits the tumor growth of 06-0606 and 10-0505 xenografts in a dose-dependent manner (P<0.01). The growth rate of 06-0606 and 10-0505 xenografts is also significantly reduced by Sorafenib. The weights of 06-0606 tumors in mice that are treated with Sorafenib 50 mg/kg and 100 mg/kg are approximately 13% and 5% of the controls, respectively. 50 mg dose of Sorafenib significantly inhibits tumor growth in mice with lines 5-1318, 26-1004 and 10-0505 (P<0.01). For 50 mg dose, the T/C ratio, where T and C are the median weight (mg) of Sorafenib- and vehicle-treated tumors at the end of the treatment, respectively, for 06-0606, 26-1004, 5-1318, and 10-0505 xenografts is 0.13, 0.10, 0.12 and 0.49, respectively. The survival rate is 73.3 % in Diethyl nitrosamine (DENA) group and 83.3 % in Sorafenib group compared to 100 % in the normal control group. DENA group shows a significant increase in liver index (1.51-fold increase, p<0.05) compared to normal control group, while treatment with Sorafenib shows significant decrease (p<0.05) in liver index when compared to DENA group. The liver index in Sorafenib group significantly decreases to lower than its value in the normal control.

相关产品:Covalent Screening Library Plus  |  Drug Repurposing Compound Library Plus  |  FDA-Approved Drug Library Plus  |  FDA-Approved Drug Library Mini  |  Bioactive Compound Library Plus  |  Apoptosis Compound Library  |  Immunology/Inflammation Compound Library  |  Kinase Inhibitor Library  |  MAPK Compound Library  |  Protein Tyrosine Kinase Compound Library  |  FDA-Approved Drug Library  |  Anti-Cancer Compound Library  |  CNS-Penetrant Compound Library  |  Autophagy Compound Library  |  Anti-Aging Compound Library  |  Drug Repurposing Compound Library  |  Covalent Screening Library  |  Differentiation Inducing Compound Library  |  Reprogramming Compound Library  |  Oxygen Sensing Compound Library  |  Ferroptosis Compound Library  |  Anti-COVID-19 Compound Library  |  Orally Active Compound Library  |  Glutamine Metabolism Compound Library  |  FDA Approved & Pharmacopeial Drug Library  |  Anti-Breast Cancer Compound Library  |  Anti-Lung Cancer Compound Library  |  Drug-Induced Liver Injury (DILI) Compound Library  |  Anti-Pancreatic Cancer Compound Library  |  Anti-Blood Cancer Compound Library  |  Targeted Therapy Drug Library   |  MG-132  |  Erastin  |  Ferrostatin-1  |  Cisplatin  |  LY294002  |  Doxorubicin hydrochloride  |  Bafilomycin A1  |  Paclitaxel  |  Cycloheximide  |  Y-27632 dihydrochloride  |  RSL3  |  Acetylcysteine  |  Angiotensin II human  |  Deferoxamine mesylate  |  SP600125  |  5-Fluorouracil  |  Staurosporine  |  Bortezomib  |  Tamoxifen  |  2-Deoxy-D-glucose  |  Gemcitabine  |  Necrostatin-1  |  Verteporfin  |  Decitabine  |  Actinomycin D  |  Temozolomide  |  BAY 11-7082  |  Etoposide  |  Mitomycin C

品牌介绍:
•   MCE (MedChemExpress) 拥有数百种全球独家化合物,我们致力于为全球科研客户提供*新*全的高品质小分子活性化合物;
•   10,000 多种高选择性抑制剂、激动剂涉及各热门信号通路及疾病领域;
•   设有专业的实验中心和严格的质控、验证体系;
•   提供 LC/MS、NMR、HPLC、手性分析、元素分析等各项质检报告,确保产品的高纯度、高品质;
•   产品的生物活性多经各国客户实验验证;
•   Nature, Cell, Science 等多种期刊及制药收录了MCE客户的科研成果;
•   专业团队跟踪*新的制药及生命科学研究进展,为您提供全球*新的活性化合物;
•   与世界各大制药公司及知名科研机构建立了长期的合作。

1000+ Inhibitors&Agonists 作用于20多条经典信号通路
30+ Screening Libraries 疾病机制研究的高效工具
CCK8 Kit | Cell Counting Kit-8
FDA-Approved 药物筛选库
Inhibitor Cocktails 蛋白酶, 磷酸酶 & 去乙酰化酶
Top Publications Citing Use of MCE
MCE Hotline: 4008203792 | 中国现货 - 全球文献引用 - 高纯度高品质 - 全方位技术支持
联系方式:
电话:021-58955995 手机:13611715263 联系人:客服部   Q Q:4008203792

热门标签:Nexavar 

快速导航

在线咨询

提交