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163655-37-6

中文名称 CS-2885
英文名称 MAZ51
CAS 163655-37-6
分子式 C21H18N2O
分子量 314.38
MOL 文件 163655-37-6.mol
更新日期 2024/10/28 15:49:09
163655-37-6 结构式 163655-37-6 结构式

基本信息

中文别名
化合物MAZ51
3-((4-(二甲基氨基)萘-1-基)亚甲基)吲哚啉-2-酮
英文别名
MAZ51
CS-2885
MAZ51
MAZ-51
MAZ 51
VEGFR3 Kinase Inhibitor, MAZ
3-(4-DIMETHYLAMINO-NAPHTHALEN-1-YLMETHYLENE)-1,3-DIHYDRO-INDOL-2-ONE
(3E)-3-[[4-(dimethylamino)naphthalen-1-yl]methylidene]-1H-indol-2-one
(3E)-3-{[4-(Dimethylamino)-1-naphthyl]methylene}-1,3-dihydro-2H-indol-2-one
2H-Indol-2-one, 3-[[4-(dimethylamino)-1-naphthalenyl]methylene]-1,3-dihydro-

物理化学性质

储存条件2-8°C
溶解度DMSO: 11 mg/mL
形态solid
颜色orange

安全数据

危险性符号(GHS)GHS hazard pictograms
GHS07
警示词警告
危险性描述H302-H315-H319-H335
危险品标志Xn,N
危险类别码22-37/38-41-51/53
安全说明26-39-61
危险品运输编号UN 3077 9/PG 3

图谱信息

常见问题列表

生物活性
MAZ51 是一种选择性的 vascular endothelial growth factor receptor (VEGFR)-3 (Flt-4) tyrosine kinase 的有效抑制剂。MAZ51 通过 Akt/GSK3β 的磷酸化和 RhoA 的激活来诱导神经胶质瘤细胞的细胞圆缩和G2/M细胞周期停滞。 MAZ51 可抑制多种非VEGFR-3表达肿瘤细胞的增殖并诱导其凋亡。
靶点
TargetValue
VEGFR-3
()
Akt
()
GSK3β
()
RhoA
()
体外研究

MAZ51 (2.5-10 μM; 24 hours) blocks proliferation and induces apoptosis in a wide variety of tumor cells.
MAZ51 (0.5-50 μM; 25 minutes) has no effect on ligand-induced autophosphorylation of EGFR, IGF-1R and PDGFRβ in A431 cells, HEK-293 cells, and PAE cells, respectively.

Cell Proliferation Assay

Cell Line: MT450, 1AS, ASM, G, AT6.1, MTLN3, MTLY, NM-081 cells
Concentration: 2.5, 10 μM
Incubation Time: 24 hours
Result: Induced apoptosis in a wide variety of tumor cells.

Apoptosis Analysis

Cell Line: MT450, 1AS, ASM, G, AT6.1, MTLN3, MTLY, NM-081 cells
Concentration: 2.5, 10 μM
Incubation Time: 24 hours
Result: Blocked proliferation in a wide variety of tumor cells.
体内研究

MAZ51 (8 mg/kg; i.p.; daily for 15 day) significantly suppresses the growth of MT450 tumors.

Animal Model: Wistar Furth rats (bearing MT450 cells)
Dosage: 8 mg/kg
Administration: Intraperitoneal injection; daily for 15 day
Result: Significantly suppressed the growth of MT450 tumors.
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