Coumurrayin

Coumurrayin
Product Name Coumurrayin
CAS No.: 17245-25-9
Catalog No.: CFN99811
Molecular Formula: C16H18O4
Molecular Weight: 274.3 g/mol
Purity: >=98%
Type of Compound: Coumarins
Physical Desc.: Powder
Source: The herbs of Murraya paniculata (L.) Jack
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Coumurrayin may have anticoagulant activity.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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    The rodenticidal activity, expressed by LD50 values of ether and petroleum ether extracts of Citrus bergamina pulp against two rat species, Rattus norvegicus (Norway rat) and Rattus rattus (roof rat) was evaluated.
    METHODS AND RESULTS:
    Based on LD50 values, ether extract was nearly 1.6 and 1.3 times more toxic to Norway rat and roof rat than ethanol respectively, while pet. ether extract was non toxic to the two rat species. From ether extract, two natural coumarines, Bergapten and Coumurrayin were isolated and tried against the two rat species as anticoagulant rodenticides. Norway rats were more susceptible to both compounds than the roof ones.
    CONCLUSIONS:
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    METHODS AND RESULTS:
    A new pyranocoumarin, named secryptotaenin A, determined as 3'(S)-angeloyloxy-3',4'-dihydroseselin, was isolated from the roots of Selinum cryptotaenium, along with thirteen known compounds, umbelliferone, osthol, Coumurrayin, (+)-heraclenol, longshengensin A, anomalin, ferulic acid, galactitol, stearic acid, melissic acid, lignoceric acid, beta-sitosterol and daucosterol.
    CONCLUSIONS:
    Their structures were determined on the basis of spectroscopic methods.
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