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首页-小分子抑制剂&激动剂-Metabolic Enzyme/Protease-Phospholipase-VU0155069
VU0155069

Chemical Structure : VU0155069

CAS No.: 1130067-06-9

VU0155069 (VU 0155069, CAY10593)

货号: PC-63190Not For Human Use, Lab Use Only.

VU0155069 is a potent, selective phospholipase D1 (PLD1) inhibitor with IC50 of 46 nM, 20-fold selectivity over PLD2 (IC50=933 nM).

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25 mg ¥1980 In stock
50 mg ¥3280 In stock
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纯度 & COA & 质检文件 纯度: >98% (HPLC) Select Batch:

生物&药学活性

VU0155069 is a potent, selective phospholipase D1 (PLD1) inhibitor with IC50 of 46 nM, 20-fold selectivity over PLD2 (IC50=933 nM).
VU0155069 sensitizes MCF7 and MDA-MB-231 breast cancer cells to doxorubicin-induced cytotoxicity.
VU0155069 suppresses growth of colorectal cancer activated by the Wnt/β-catenin and PI3K signaling pathways.

物理化学性质&存储条件

分子量 462.978
分子式 C26H27ClN4O2
外观性状 Solid
CAS No.
储存条件
固体粉末
-20 °C 12 个月; 4°C 6 个月
配置液
-80 °C 6 个月; -20°C 6 个月
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

N-[(1S)-2-[4-(5-Chloro-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-1-piperidinyl]-1-methylethyl]-2-naphthalenecarboxamide

参考文献

1. Scott SA, et al. Nat Chem Biol. 2009 Feb;5(2):108-17.

2. Song HI, et al. Sci Rep. 2016 Nov 22;6:36968.

3. Kang DW, et al. Clin Cancer Res. 2017 Dec 1;23(23):7340-7350.

4. Cheng M, et al. Neoplasia. 2017 Aug;19(8):617-627.

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