Confluentic acid

Confluentic acid
Product Name Confluentic acid
CAS No.: 6009-12-7
Catalog No.: CFN97015
Molecular Formula: C28H36O8
Molecular Weight: 500.6 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Powder
Targets: MAO
Source: The herbs of Himatanthus sucuuba
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Confluentic acid shows selective inhibition of Monoamine oxidase B with IC50 value of 0.22 microM.
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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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  • Korea Institute of Oriental Medicine2020, doi: 10.21203.
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  • J of the Korean Society of Food Science and Nutrition2016, 45(7):1017-1025
  • Front Microbiol.2022, 12:833233.
  • Appl. Sci.2023, 13(17):9984.
  • Anal Chim Acta.2021, 1180:338874.
  • Pharmaceuticals (Basel).2024, 18(1):19.
  • Int J Mol Sci.2023, 24(24):17589.
  • Int Immunopharmacol.2021, 100:108073.
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    Monoamine oxidase B (MAO-B) inhibitors were isolated from the bark of a Brazilian plant, Himatanthus sucuuba (SPR.).
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    Assignments of the 1H- and 13C-NMR data using two dimensional (2D)-NMR techniques showed the active components to be known lichen depsides, Confluentic acid (1) and 2'-O-methylperlatolic acid (2).
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