Moscatin

Moscatin
Product Name Moscatin
CAS No.: 108335-06-4
Catalog No.: CFN93148
Molecular Formula: C15H12O3
Molecular Weight: 240.25 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Powder
Source: The herbs of Dendrobium nobile Lindl.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $318/5mg
Moscatin exhibits antiplatelet aggregation 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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    J Nat Prod. 1994 Sep;57(9):1271-4.
    Antiplatelet aggregation principles of Dendrobium loddigesii.[Pubmed: 7798962]

    METHODS AND RESULTS:
    The MeOH extract of the stem of Dendrobium loddigesii was found to inhibit the aggregation of rabbit platelets induced by arachidonic acid and collagen.
    CONCLUSIONS:
    Two active compounds, moscatilin [1] and Moscatin [2], were isolated. Moscatilin diacetate [3] also exhibited antiplatelet aggregation activity.
    Zhong Yao Cai. 2015 Mar;38(3):514-7.
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    To investigate the chemical constituents in the ethanol extract from the whole plant of Euphorbia lunulata.
    METHODS AND RESULTS:
    The whole plant of Euphorbia lunulata was extracted by 95% ethanol, then partitioned by system solvents with different polarity. The ethyl acetate and n-butyl alcohol extracts were separated on silica gel, Sephadex LH-20,and MCI columns. The isolated compounds were determined by detailed analysis of their spectral data. Twelve compounds were isolated and identified from the ethyl acetate and n-butyl alcohol extracts of Euphorbia lunulata and the structures were identified as 7β-methoxy-stigmast-5-ene-3β-ol (1), 7β-methoxy-stigmast-5-ene-3β,22β-diol(2), asperglaucide(3), Moscatin (4), p-hydroxybenzoic acid (5),3-methoxy-4-hydroxy benzoic acid(6), erigeside C(7),5,7,4'-trihydroxy flavanone(8), kaempferol(9), quercetin(10), corosolic acid(11) and acacetin (12).
    CONCLUSIONS:
    All compounds except for 9 and 10 are reported from this plant for the first time.
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