COUMARIN

Coumarin is a natural compound with anticoagulant and fragrance applications. It modulates vitamin K⁺ pathways. Side effects include liver toxicity at high doses. Only GMP materials will be supplied, logistics all according to GDP.

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Product Description


Mechanism of Action

Coumarin is a benzopyrone compound with anticoagulantrelated structural properties, though the parent compound itself does not strongly inhibit vitaminK recycling. It modulates cytochrome P450 enzymes, exhibits antioxidant activity, and influences inflammatory and calciumsignalling pathways. It is also a precursor for numerous pharmacologically active derivatives.

Benefits and Advantages

Used in flavonoid/coumarin SAR research, cytochromemodulation assays, phototoxicity studies, naturalproduct biosynthesis modelling, and anticoagulantderivative development.

Side Effects and Risks

Risks include hepatotoxicity at high doses, photosensitivity, enzymeinteraction effects and allergenic potential. Handle with naturalproduct compound precautions.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C9H6O2

Molecular Weight

146.14 g/mol

CAS Number

91-64-5

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

less than 0.1 mg/mL at 63.5 °F (NTP, 1992)

Purity

Purity information is available upon request (COA).

Synonym

coumarin; 91-64-5; 2H-Chromen-2-one; 2H-1-Benzopyran-2-one; cumarin

IUPAC/Chemical Name

chromen-2-one

InChl Key

ZYGHJZDHTFUPRJ-UHFFFAOYSA-N

InChl Code

InChI=1S/C9H6O2/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H

References

https://pubchem.ncbi.nlm.nih.gov/compound/323;

3D Conformer.

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