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528283  Polo-like Kinase Inhibitor II, BTO-1

5-Cyano-7-nitro-2-(benzothiazolo-N-oxide)-carboxamide

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04 February 2012

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528283-2MG  2 mg 
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A cell-permeable benzothiazolo-N-oxide compound that targets the ATP-binding pocket of polo-like kinase and is shown to inhibit Plk1 kinase activity in cell-free kinase assays (IC50 = 8.0 µM) and suppress the phosphorylation of cellular Plk1 substrate Cdc25C in rat kangaroo kidney-derived PTK cells (75% inhibition at 6.3 µM). BTO-1 treatment of cultured cells results in mitosis defects consistent with loss-of-Plk1 phenotypes seen in Plk1 RNAi-treated U20S cells, including the appearance of monopolar spindles and the reduction of γ-tubulin at the centrosomes. Plk1 inhibition by BTO-1 in HeLa cells results in a blockage of Rho and Rho-GEF recruitment, which is essential for the assembly of a functional contractile ring.
Product information
Form Beige solid
Molar mass 264.2
Protect from Light Yes
Packaged under inert gas Yes
Purity ≥97% by HPLC
Solubility DMSO
Chemical formula C9H4N4O4S
CAS number 40647-02-7
Store and ship information
Storage +2°C to +8°C
Ship Ambient Temperature Only
Harmful
Safety information
S Phrase S: 26-36/37

In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
Wear suitable protective clothing and gloves.
R Phrase R: 20/21/22-36/37/38

Harmful by inhalation, in contact with skin and if swallowed.
Irritating to eyes, respiratory system and skin.
Polo-like Kinase Inhibitor II, BTO-1, molecular structure

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© Merck KGaA, Darmstadt, Germany, 2012

All references to Merck refer to Merck KGaA, Darmstadt, Germany.

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