ABT-751

产品说明书

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Chemical Structure| 141430-65-1 同义名 : E7010
CAS号 : 141430-65-1
货号 : A110139
分子式 : C18H17N3O4S
纯度 : 99%+
分子量 : 371.41
MDL号 : MFCD00910291
存储条件:

Pure form Sealed in dry,2-8°C

In solvent -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 105 mg/mL(282.71 mM),配合低频超声助溶,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:

IP 2% DMSO+2% Tween80+30% PEG300+water 4.2 mg/mL clear

PO 0.5% CMC-Na 34 mg/mL suspension

生物活性
描述 ABT-751 is a bioavailable tubulin-binding and antimitotic sulfonamide agent with IC50 of about 1.5 and 3.4 μM in neuroblastoma and non-neuroblastoma cell lines, respectively.
细胞研究
细胞系 浓度 检测类型 检测时间 活性说明 数据源
A2780 cells Cytotoxicity assay 48-72 h Cytotoxicity against human A2780 cells after 48 to 72 hrs by WAT-1 assay, IC50=0.17 μM 21126027
A549 cells Proliferation assay 24 h Antiproliferative activity against human A549 cells assessed as growth inhibition after 24 hrs by SRB assay, GI50=1.31 μM 25468039
ACHN cells Cytotoxicity assay 48 h Cytotoxicity against human ACHN cells after 48 hrs by MTT assay, IC50=2.13 μM 24835786
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

2.69mL

0.54mL

0.27mL

13.46mL

2.69mL

1.35mL

26.92mL

5.38mL

2.69mL

参考文献

[1]Aggarwal C, Somaiah N, et al. Antiangiogenic agents in the management of non-small cell lung cancer: where do we stand now and where are we headed? Cancer Biol Ther. 2012 Mar;13(5):247-63. doi: 10.4161/cbt.19594.

[2]Huang SM, Mishina YM, et al. Tankyrase inhibition stabilizes axin and antagonizes Wnt signalling. Nature. 2009 Oct 1;461(7264):614-20.