Daurichromenic acid

Daurichromenic acid
Product Name Daurichromenic acid
CAS No.: 82003-90-5
Catalog No.: CFN97302
Molecular Formula: C23H30O4
Molecular Weight: 370.5 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Powder
Targets: HIV
Source: The herbs of Rhododendron dauricum
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Daurichromenic acid is a terpenophenol with a potent anti-HIV 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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    Nat Prod Commun. 2014 Sep;9(9):1329-32.
    Daurichromenic acid-producing oxidocyclase in the young leaves of Rhododendron dauricum.[Pubmed: 25918805]
    Rhododendron dauricum L., a flowering tree popular in Hokkaido, produces Daurichromenic acid (DCA), a terpenophenol with a potent anti-HIV activity.
    METHODS AND RESULTS:
    The Daurichromenic acid-producing enzyme, named Daurichromenic acid synthase, could be detected in the soluble protein fraction prepared from the young leaves of R. dauricum. Daurichromenic acid synthase catalyzed oxidocyclization of the farnesyl group of grifolic acid to form (+)-Daurichromenic acid as the major reaction product.
    CONCLUSIONS:
    The Daurichromenic acid synthase reaction proceeds without the need for any cofactors and coenzymes except for molecular oxygen. Interestingly, these catalytic properties of Daurichromenic acid synthase are quite similar to those reported for cannabinoid synthases in the marijuana plant Cannabis sativa L.
    Org Lett. 2003 Nov 13;5(23):4481-4.
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    METHODS AND RESULTS:
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