货号:A264992
同义名:
CH5424802,艾乐替尼
/ CH5424802;RO5424802
Alectinib(CH5424802)是一种有效、选择性的口服ALK抑制剂,IC50为1.9 nM,Kd值为2.4 nM(以ATP竞争性方式),还以1 nM和3.5 nM的IC50值抑制ALK F1174L和ALK R1275Q。Alectinib显示出有效的中枢神经系统(CNS)渗透性。
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产品名称 | ALK ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ASP3026 |
+
ALK, IC50: 3.5 nM |
99%+ | |||||||||||||||||
ALK-IN-1 |
++++
ALK, IC50: 0.07 nM |
99%+ | |||||||||||||||||
Crizotinib |
++++
ROS1, Ki: <0.025 nM ALK, IC50: 24 nM |
99%+ | |||||||||||||||||
Entrectinib | ✔ | 99%+ | |||||||||||||||||
Brigatinib |
+++
ROS1, IC50: 1.9 nM ALK, IC50: 0.37 nM |
FLT3 | 98% | ||||||||||||||||
NVP-TAE 684 |
+
ALK, IC50: 3 nM |
99%+ | |||||||||||||||||
Alectinib |
++
ALK, IC50: 1.9 nM ALK (F1174L), IC50: 3.5 nM |
98% | |||||||||||||||||
Ceritinib |
+++
ALK, IC50: 0.2 nM |
Insulin Receptor,IGF-1R | 98% | ||||||||||||||||
GSK1838705A |
+++
ALK, IC50: 0.5 nM |
Insulin Receptor,IGF-1R | 99% | ||||||||||||||||
AZD-3463 |
++
ALK, Ki: 0.75 nM |
IGF-1R | 99% | ||||||||||||||||
Lorlatinib |
++++
ROS1, Ki: <0.07 nM ALK (L1196M), Ki: 0.07 nM |
98% | |||||||||||||||||
Repotrectinib |
+
ALK(G1202R), IC50: 1.26 nM ALK(L1196M), IC50: 1.01 nM |
Src | 99% | ||||||||||||||||
Belizatinib |
++
ALK, IC50: 0.7 nM |
99%+ | |||||||||||||||||
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 |
靶点 |
|
描述 | ALK (anaplastic lymphoma kinase) is a tyrosine kinase that is constitutively activated in certain cancers, following gene alterations such as chromosomal translocation, amplification or point mutation. Alectinib is a potent and selective ALK inhibitor with IC50 value of 1.9nM (measured by enzyme activity). Alectinib was preferentially efficacious against NCI-H2228 cells expressing EML4-ALK, but not ALK fusion-negative NSCLC cell lines, including HCC827 cells (EGFR exon 19 deletion), A549 cells (KRAS mutant), or NCIH522 cells (EGFR wild-type, KRAS wild-type, and ALK wildtype) in monolayer culture. Consistent with that, Alectinib can prevent autophosphorylation of ALK and thus resulted in substantial suppression of phosphorylation of STAT3 and AKT, but not of ERK1/2, in NCI-H2228 NSCLC cells expressing EML4-ALK, but not in ALK fusion-negative A549 cells. The potent inhibition of ALK kinase activity by Alectinib can also be observed in vivo. Oral administration of Alectinib caused dose-dependent decrease of pSTAT3-Tyr705 and pAKT-Ser473 in tumors from mice bearing NCI-H2228 cells at dose < 20mg/kg, with a significant decrease in the expression of STAT3 target genes, such as BCL3, NNMT, SOCS3 and BCL2L1, at dose of 6mg/kg. Administered CH5424802 orally once daily for 11 days at dose 2, 6 and 20mg/kg inhibited tumor growth dose-dependently, with decreased pALK-Tyr1604, in mice bearing NCI-H2228 but not A549. The maximum efficacy can be observed at dose of 60mg/kg for 3 weeks and a prolonged effect with no regrowth of tumor for 4 weeks in this model. Therapeutic efficacy of Alectinib on tumor regression can also be observed in models generated by implantation of KARPAS-299 ALCL cells and NB-1 neuroblastoma cells[1]. |
作用机制 | Alectinib acts in an ATP-competitive manner and blocks the L1196M gatekeeper mutation of ALK.[1] |
细胞系 | 浓度 | 检测类型 | 检测时间 | 活动说明 | 数据源 |
22Rv1 | ~10 μM | Growth inhibitory assay | IC50>10,000 nM | 21575866 | |
Ba/F3 | ~1 μM | Function assay | suppresses phosphorylation of ERK and increases the abundance of BIM | 25349307 | |
BT-483 | ~10 μM | Growth inhibitory assay | IC50>10,000 nM | 21575866 | |
Calu-1 | ~10 μM | Growth inhibitory assay | IC50>10,000 nM | 21575866 | |
Dose | Mice: min = 2 mg/kg, max = 20 mg/kg[2] (p.o.); 25 mg/kg[3] (i.p.) |
Administration | p.o., i.p. |
NCT号 | 适应症或疾病 | 临床期 | 招募状态 | 预计完成时间 | 地点 |
NCT03498521 | Cancer of Unknown Primary Site | Phase 2 | Recruiting | April 16, 2022 | - |
NCT01634763 | Tumors Characterized by Geneti... 展开 >>c Alterations in Anaplastic Lymphoma Kinase (ALK) 收起 << | Phase 1 | Completed | - | Japan ... 展开 >> Novartis Investigative Site Sunto-gun, Shizuoka, Japan, 411-8777 Novartis Investigative Site Koto, Tokyo, Japan, 135-8550 Novartis Investigative Site Fukuoka, Japan, 811-1395 收起 << |
NCT03158389 | Glioblastoma, Adult | Phase 1 Phase 2 | Recruiting | September 30, 2024 | Germany ... 展开 >> Charité Berlin, Neurosurgery Not yet recruiting Berlin, Germany Knappschaftskrankenhaus Bochum GmbH, Neurology Clinic Not yet recruiting Bochum, Germany University Hospital Bonn, Neurology Clinic Not yet recruiting Bonn, Germany University Hospital Cologne, Neurosurgery Not yet recruiting Cologne, Germany University Hospital Dresden, Neurosurgery Not yet recruiting Dresden, Germany University Hospital Essen, Neurology Clinic Not yet recruiting Essen, Germany University Hospital Frankfurt, Neurooncology Not yet recruiting Frankfurt am Main, Germany University Hospital Heidelberg, Neurology Clinic Recruiting Heidelberg, Germany University Hospital Saarland, Neurosurgery Not yet recruiting Homburg, Germany University Hospital Mainz, Neurosurgery Not yet recruiting Mainz, Germany University Hospital Mannheim, Neurology Clinic Not yet recruiting Mannheim, Germany University Hospital Regensburg, Neurology Clinic Not yet recruiting Regensburg, Germany University Hospital Tuebingen, Neurooncology Not yet recruiting Tübingen, Germany 收起 << |
计算器 | ||||
存储液制备 | ![]() |
1mg | 5mg | 10mg |
1 mM 5 mM 10 mM |
2.07mL 0.41mL 0.21mL |
10.36mL 2.07mL 1.04mL |
20.72mL 4.14mL 2.07mL |
CAS号 | 1256580-46-7 |
分子式 | C30H34N4O2 |
分子量 | 482.617 |
别名 | CH5424802,艾乐替尼 ;CH5424802;RO5424802;RG7853 |
运输 | 蓝冰 |
存储条件 |
粉末 Sealed in dry,Store in freezer, under -20°C 液体 -20°C:3-6个月-80°C:12个月 |
溶解度 |
DMSO: 2 mg/mL(4.14 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
动物实验配方 |