4-Methyldaphnetin

4-Methyldaphnetin
Product Name 4-Methyldaphnetin
CAS No.: 2107-77-9
Catalog No.: CFN93089
Molecular Formula: C10H8O4
Molecular Weight: 192.17 g/mol
Purity: >=98%
Type of Compound: Coumarins
Physical Desc.: Powder
Targets: LOX
Source: The herbs of Daphne Korean Nakai
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
4-Methyldaphnetin is a potent inhibitor (low micromolar) of lipid peroxidation and scavengers of superoxide anion radicals and of aqueous alkylperoxyl radicals, but may be pro-oxidant (enhancing generation of hydroxyl radicals) in the presence of free iron ions.4-Methyldaphnetin inhibits the proinflammatory 5-lipoxygenase enzyme at micromolar concentrations.
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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.

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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.
  • Eur J Pharmacol.2018, 832:96-103
  • Planta Med.2019, 85(9-10):766-773
  • Analytical methods2019, 11(6)
  • Chengdu University of Traditional Chinese Medicine2024, 4802935.
  • Biotechnology and Bioprocess Engineering2024, 29:1048-1060.
  • Int J Mol Sci.2021, 22(21):11836.
  • Plant Cell, Tissue and Organ Culture (PCTOC)2020, 143, 45-60(2020)
  • Phytother Res.2023, 37(10):4587-4606.
  • Immunopharmacol Immunotoxicol.2024, 46(4):496-508.
  • STAR Protoc.2024, 5(2):102990.
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    Gen Pharmacol. 1996 Jun;27(4):713-22.
    Pharmacological and biochemical actions of simple coumarins: natural products with therapeutic potential.[Pubmed: 8853310]
    5. Cloricromene, a synthetic coumarin derivative, also possesses antithrombotic antiplatelet actions, inhibits PMN neutrophil function and causes vasodilatation. Some of these properties of cloricromene have been ascribed to inhibition of arachidonate release from membrane phospholipids.
    METHODS AND RESULTS:
    6. Simple coumarins possessing ortho-dihydroxy functions, such as fraxetin and 4-Methyldaphnetin, are potent inhibitors (low micromolar) of lipid peroxidation and scavengers of superoxide anion radicals and of aqueous alkylperoxyl radicals, but may be pro-oxidant (enhancing generation of hydroxyl radicals) in the presence of free iron ions. These coumarins also inhibit the proinflammatory 5-lipoxygenase enzyme at micromolar concentrations. Another related coumarin, 5,7-dihydroxy-4-methylcoumarin, is of special interest as it inhibits lipid peroxidation, and scavenges alkylperoxyl and superoxide radicals. Unlike most other simple coumarins studied, 5,7-dihydroxy-4-methylcoumarin also scavenges hypochlorous acid, and is a potent inhibitor of cyclo-oxygenase, but is not pro-oxidant. 7. 5,7- and 6,7-dihydroxy-4-methylcoumarin both reduced the duration of ventricular fibrillation in postischaemic reperfused isolated perfused rat hearts (in which oxygen-derived free radicals are implicated), showing that these antioxidant coumarins possess beneficial properties in this pathophysiological model.
    CONCLUSIONS:
    8. In view of the established low toxicity, relative cheapness, presence in the diet and occurrence in various herbal remedies of coumarins, it appears prudent to evaluate their properties and applications further.
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