Macrocarpal D

Macrocarpal D
Product Name Macrocarpal D
CAS No.: 142647-71-0
Catalog No.: CFN99471
Molecular Formula: C28H40O6
Molecular Weight: 472.6 g/mol
Purity: >=98%
Type of Compound: Sesquiterpenoids
Physical Desc.: Yellow powder
Targets: HIV-RTase | Antifection
Source: The branches of Eucalyptus globulus
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Macrocarpal D is a HIV-RTase inhibitor. It has antibacterial 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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    Tetrahedron Letters, 1992, 33(21):2983-2986.
    Macrocarpals: HIV-RTase inhibitors of Eucalyptus globulus.[Reference: WebLink]

    METHODS AND RESULTS:
    Five HIV-RTase inhibitors, macrocarpals A-E(macrocarpal A, macrocarpal B, macrocarpal C, Macrocarpal D, macrocarpal E), have been isolated from Eucalyptus globulus. X-ray diffraction studies as well as spectral and chemical investigations established the structures 1, 2, 3, 12, and 13, respectively.
    Journal of the Agricultural Chemical Society of Japan, 1992, 56(10):1570-1576.
    Isolation and Characterization of Macrocarpals B—G Antibacterial Compounds from Eucalyptus macrocarpa.[Reference: WebLink]

    METHODS AND RESULTS:
    Six novel phloroglucinol dialdehyde diterpene derivatives (macrocarpal B, macrocarpal C, Macrocarpal D, macrocarpal E, macrocarpal F, macrocarpal G), which have antibacterial activity, were isolated from leaves of Eucalyptus macrocarpa. These compounds have closely related structures, the molecular formula for B—F being C28H40O6, and that of G being C28H38O5.
    CONCLUSIONS:
    The structures of macrocarpals B, D, and G were analyzed by means of NMR analyses.
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