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287897  Dicoumarol

3,3′-Methylenebis(4-hydroxycoumarin), Bishydroxycoumarin, Dicumarol

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25 May 2012

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Product number Qty/Pk Quantity Price Delivery Date
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287897-500MG  500 mg 
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A cell-permeable quinone reductase inhibitor with anticoagulant properties. Potentiates apoptosis by simultaneously blocking SAPK/JNK and NF-κB pathways. Does not affect phosphorylation of p38 or activation of AKT. Blocks brefeldin A-dependent mono-ADP-ribosylation in vitro and Golgi disassembly in living cells (IC50 = 180 µM and 150 µM, respectively).
Product information
Form White solid
Primary Target Blocks brefeldin A-dependent mono-ADP-ribosylation in vitro
Primary Target IC50 180 µM
Secondary target Golgi disassembly in living cells IC50 = 150 µM
Molar mass 336.3
Protect from Light Yes
Packaged under inert gas Yes
Purity ≥98% by titration
Solubility Aqueous alkaline solutions or organic bases
Chemical formula C19H12O6
RTECS GN7875000
CAS number 66-76-2
Merck USA index 14, 3090
Store and ship information

Hazardous Materials Attention: Due to the nature of the Hazardous Materials in this shipment, additional shipping chargesmay be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.

Storage +2°C to +8°C
Ship Ambient Temperature Only
Toxic & Carcinogenic / Teratogenic
Safety information
S Phrase S: 37-45-61

Wear suitable gloves.
In case of accident or if you feel unwell, seek medical advice immediately (show the label where possible).
Avoid release to the environment. Refer to special instructions/safety data sheet.
R Phrase R: 22-48/25-51/53

Harmful if swallowed.
Toxic: danger of serious damage to health by prolonged exposure if swallowed.
Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
Dicoumarol, molecular structure

© Merck KGaA, Darmstadt, Germany, 2012

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


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