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VU0155069

Chemical Structure : VU0155069

CAS No.: 1130067-06-9

VU0155069 (VU 0155069, CAY10593)

Catalog No.: 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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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

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.

Physicochemical Properties

M.Wt 462.978
Formula C26H27ClN4O2
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
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

References

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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