PZ0191
克唑替尼
≥98% (HPLC), c-Met (hepatocyte growth factor receptor) inhibitor, powder
别名:
PF 2341066, PF-02341066, PF02341066, 克唑替尼, （R）-3-[1-（2,6-二氯-3-氟 - 苯基）-乙氧基]-5-（1-哌啶-4-基-1H-吡唑-4-基）-吡啶-2-基胺
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关于此项目
经验公式（希尔记法）:
C21H22Cl2FN5O
CAS Number:
分子量:
450.34
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
Product Name
克唑替尼, ≥98% (HPLC)
质量水平
方案
≥98% (HPLC)
表单
powder
颜色
white to tan
储存温度
room temp
SMILES字符串
C[C@@H](Oc1cc(cnc1N)-c2cnn(c2)C3CCNCC3)c4c(Cl)ccc(F)c4Cl
InChI
1S/C21H22Cl2FN5O/c1-12(19-16(22)2-3-17(24)20(19)23)30-18-8-13(9-27-21(18)25)14-10-28-29(11-14)15-4-6-26-7-5-15/h2-3,8-12,15,26H,4-7H2,1H3,(H2,25,27)/t12-/m1/s1
InChI key
KTEIFNKAUNYNJU-GFCCVEGCSA-N
相关类别
应用
克唑替尼已被用于：
- 研究其对肝细胞生长因子受体（c-Met）表达、增殖和凋亡的影响
- 阻断上皮细胞中神经营养性酪氨酸激酶1型受体（NTRK1）的活性
- 恢复对厄洛替尼的敏感性
生化/生理作用
ATP 竞争性 c-MET/ALK 抑制剂
克唑替尼（PF-02341066）是受体酪氨酸激酶（RTKs）c-Met（肝细胞生长因子受体）和间变性淋巴瘤激酶（ALK）的 ATP 竞争性抑制剂。在 > 120 种研究过的不同的 RTK 中，克唑替尼是一种高度特异性的 c-Met 和 ALK 抑制剂。克里唑蒂尼被批准用于治疗具有 ALK 融合突变的非小细胞肺癌（NSCLC）亚型。
特点和优势
这种化合物是激酶磷酸酶生物学研究的特色产品。点击此处发现更多特色激酶磷酸酶生物产品。在sigma.com/discover-bsm可了解更多关于生物活性小分子的其他研究领域。
警示用语：
Warning
危险分类
Aquatic Acute 1 - Eye Irrit. 2 - Muta. 2 - Skin Sens. 1
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Nicole R Infarinato et al.
Cancer discovery, 6(1), 96-107 (2015-11-12)
Neuroblastomas harboring activating point mutations in anaplastic lymphoma kinase (ALK) are differentially sensitive to the ALK inhibitor crizotinib, with certain mutations conferring intrinsic crizotinib resistance. To overcome this clinical obstacle, our goal was to identify inhibitors with improved potency that
Neurotrophic tyrosine kinase receptor 1 is a direct transcriptional and epigenetic target of IL-13 involved in allergic inflammation
Rochman M, et al.
Mucosal Immunology, 8(4), 785-785 (2015)
Damini Chand et al.
Disease models & mechanisms, 6(2), 373-382 (2012-10-30)
Neuroblastoma is a childhood extracranial solid tumour that is associated with a number of genetic changes. Included in these genetic alterations are mutations in the kinase domain of the anaplastic lymphoma kinase (ALK) receptor tyrosine kinase (RTK), which have been
Zheng Liu et al.
Oncoimmunology, 9(1), 1758003-1758003 (2020-09-15)
Despite some of the oncogenic driver mutations that have been associated with increased expression of programmed death-ligand 1 (PD-L1), the correlation between PD-L1 expression and ROS1 fusion in NSCLC cells, especially for those with Crizotinib resistance has not been fully
Shota Yamamoto et al.
Radiology, 272(2), 568-576 (2014-06-03)
To present a radiogenomic computed tomographic (CT) characterization of anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer (NSCLC) (ALK+). In this HIPAA-compliant institutional review board-approved retrospective study, CT studies, ALK status, and clinical-pathologic data in 172 patients with NSCLC from
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