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Key Documents

M1390

Sigma-Aldrich

3,3′-Methylene-bis(4-hydroxycoumarin)

Synonyme(s) :

Bishydroxycoumarin, Dicoumarol, Dicumarol

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About This Item

Formule empirique (notation de Hill):
C19H12O6
Numéro CAS:
Poids moléculaire :
336.29
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352103
ID de substance PubChem :
Nomenclature NACRES :
NA.47

Source biologique

synthetic (organic)

Niveau de qualité

Pureté

≥98% (TLC)

Forme

powder

Pf

290-292 °C (lit.)

Solubilité

pyridine: 50 mg/mL, clear, faintly yellow to brownish-yellow

Chaîne SMILES 

OC1=C(CC2=C(O)c3ccccc3OC2=O)C(=O)Oc4ccccc14

InChI

1S/C19H12O6/c20-16-10-5-1-3-7-14(10)24-18(22)12(16)9-13-17(21)11-6-2-4-8-15(11)25-19(13)23/h1-8,20-21H,9H2

Clé InChI

DOBMPNYZJYQDGZ-UHFFFAOYSA-N

Informations sur le gène

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Actions biochimiques/physiologiques

Prototype of the 4-hydroxycoumarin class of anticoagulants, which act as vitamin K antagonists, preventing formation of prothrombin. There are many reports that dicumarol also inhibits NADPH:quinone oxidoreductase (NQO(1)). In one, it inhibited NQO(1) in a pancreatic cancer cell line, causing increased formation of superoxide and inhibiting cell growth.

Pictogrammes

Skull and crossbonesHealth hazardEnvironment

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 3 Oral - Aquatic Chronic 2 - STOT RE 1 Oral

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Biochemical pharmacology, 81(3), 355-363 (2010-10-26)
The enzyme NAD(P)H quinone oxidoreductase (NQO1) can function both as a detoxifying enzyme as well as chaperone protein. The latter property has been extensively characterized by the use of dicoumarol which inhibits the chaperone properties of NQO1 in cells. However
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