Alectinib Hydrochloride
Cat.No:IA3070 Solarbio
CAS:1256589-74-8
Storage:Powder:2-8℃,2 years
Purity:≥98%
Appearance:White to off-white Solid
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Alectinib HydrochlorideCAS:1256589-74-8
Storage:Powder:2-8℃,2 years
Purity:≥98%
Appearance:White to off-white Solid
Qty:
Size:
CAS | 1256589-74-8 |
Name | Alectinib Hydrochloride |
Molecular Formula | C30H34N4O2·HCl |
Molecular Weight | 519.08 |
Solubility | Soluble in DMSO ≥0.1mg/mL(Need ultrasonic) |
Purity | ≥98% |
Appearance | White to off-white Solid |
Storage | Powder:2-8℃,2 years |
MDL | MFCD27987893 |
SMILES | [H]Cl.N#CC1=CC2=C(C3=C(N2)C(C)(C4=CC(N5CCC(CC5)N6CCOCC6)=C(C=C4C3=O)CC)C)C=C1 |
Target Point | ALK |
Passage | Protein Tyrosine Kinase/RTK;Angiogenesis |
Background | Alectinib Hydrochloride is a potent and selective ALK inhibitor. |
Biological Activity | Alectinib (AF802, CH5424802, RO5424802, RG-7853)是一种选择性抑制ALK酪氨酸激酶的口服药物,IC50为1.9 nM。[1] |
In Vitro | Alectinib抑制ALK,IC50为1.9 nM,相对其他丝氨酸/苏氨酸激酶,对ALK具有高选择性。对于耐crizotinib的ALK突变,如L1196M、F1174L、R1275Q和C1156Y,Alectinib也十分有效。在KARPAS-299(lymphoma),NB-1(neuroblastoma)和 NCI-H2228(lung cancer)ALK阳性的细胞系中,alectinib可抑制其细胞增殖,IC50分别为3、4.5和53 nM[1]。 |
In Vivo | 口服给药浓度为2-20 mg/kg(q.d.)时,Alectinib可浓度依赖性的抑制EML4-ALK阳性的NCI-H2228异种移植瘤,在EML4-ALK L1196M驱动的肿瘤中也有显著的效果[1]。在具有ALK基因突变(改变)的癌症中,Alectinib具有抗肿瘤活性[2]。 |
Cell Experiment | Animal Models: 通过皮下接种肿瘤的SCID小鼠;Dosages: 60 mg/kg;Administration: 口服[2] |
Data Literature Source | [1] Song Z,et al. Acta Pharm Sin B. 2015,5(1):34-7. [2] Kodama T,et al. Cancer Lett. 2014,351(2):215-21. [3] Ke Yang,et al. Exp Mol Med. 2017,49(3): e303. |
Unit | Bottle |
Specification | 10mg 25mg |
是一种有效、选择性 ALK 抑制剂。
Remark:These protocols are for reference only. Solarbio does not independently validate these methods.
Note:
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3. The experimental results may be affected by many factors, after-sale service is limited to the product itself and does not involve other compensation.
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