Macrocarpal H

Macrocarpal H
Product Name Macrocarpal H
CAS No.: 179388-53-5
Catalog No.: CFN99841
Molecular Formula: C28H40O6
Molecular Weight: 472.6 g/mol
Purity: >=98%
Type of Compound: Sesquiterpenoids
Physical Desc.: Yellow powder
Targets: Antifection
Source: The branch of Eucalyptus globulus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Macrocarpal H has anti-glucosyltransferase, and anti-bacterial activities.
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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.
  • Wageningen University & Research2018, January 2018
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  • Macrocarpal H

    Catalog No: CFN99841
    CAS No: 179388-53-5
    Price: Inquiry(manager@chemfaces.com)
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    J Nat Prod. 1996 Sep;59(9):823-7.
    Macrocarpals H, I, and J from the Leaves of Eucalyptus globulus[Pubmed: 8864235 ]

    METHODS AND RESULTS:
    A 50% EtOH extract of Eucalyptus globulus leaves yielded eight phloroglucinol--sesquiterpene-coupled constituents, including three novel compounds named Macrocarpal H, macrocarpal I, and macrocarpal J.
    CONCLUSIONS:
    Some of these compounds possessed antibacterial activity against oral pathogenic microorganisms with MIC values ranging from 0.20 micrograms/mL to 6.25 micrograms/mL. Inhibition of glucosyltransferase activity by these compounds was also noted.
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