Wedelolactone

For research use only. Not for therapeutic Use.

  • CAT Number: R006650
  • CAS Number: 524-12-9
  • Molecular Formula: C16H10O7
  • Molecular Weight: 314.25
  • Purity: ≥95%
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Wedelolactone(Cat No.:R006650)is a bioactive compound found in several medicinal plants, particularly in Eclipta alba, known for its hepatoprotective and anti-inflammatory properties. It is a lignan-like flavonoid that has demonstrated antioxidant effects by scavenging free radicals and reducing oxidative stress. Wedelolactone has been studied for its potential to treat liver diseases, as it can help prevent liver damage and promote regeneration. Additionally, it shows promise in reducing inflammation, inhibiting fibrosis, and possibly offering anticancer activity. It is also investigated for its neuroprotective and cardioprotective effects, although more clinical studies are needed to confirm its efficacy.


Catalog Number R006650
CAS Number 524-12-9
Synonyms

1,8,9-trihydroxy-3-methoxy-[1]benzofuro[3,2-c]chromen-6-one

Molecular Formula C16H10O7
Purity ≥95%
Target Metabolic Enzyme/Protease
IUPAC Name 1,8,9-trihydroxy-3-methoxy-[1]benzofuro[3,2-c]chromen-6-one
InChI InChI=1S/C16H10O7/c1-21-6-2-10(19)14-12(3-6)23-16(20)13-7-4-8(17)9(18)5-11(7)22-15(13)14/h2-5,17-19H,1H3
InChIKey XQDCKJKKMFWXGB-UHFFFAOYSA-N
SMILES COC1=CC(=C2C(=C1)OC(=O)C3=C2OC4=CC(=C(C=C43)O)O)O
Reference

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<span style=”font-size:12px;”><span style=”caret-color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>2.Li, C.C., et al. 2003.&nbsp;</span><i style=”caret-color: rgb(68, 68, 68); color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>J. Org. Chem.</i><span style=”caret-color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>&nbsp;</span><b style=”caret-color: rgb(68, 68, 68); color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>68,</b><span style=”caret-color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>&nbsp;8500.</span><br style=”caret-color: rgb(68, 68, 68); color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;” />
<span style=”caret-color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>3.Mors, W.B., et al. 1989.&nbsp;</span><i style=”caret-color: rgb(68, 68, 68); color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>Toxicon</i><span style=”caret-color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>&nbsp;</span><b style=”caret-color: rgb(68, 68, 68); color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>27,</b><span style=”caret-color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>&nbsp;1003.</span><br style=”caret-color: rgb(68, 68, 68); color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;” />
<span style=”caret-color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>4.Wagner, H., and Fessler, B. 1986.&nbsp;</span><i style=”caret-color: rgb(68, 68, 68); color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>Planta Med.</i><span style=”caret-color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>&nbsp;</span><b style=”caret-color: rgb(68, 68, 68); color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>5,</b><span style=”caret-color: rgb(68, 68, 68); font-family: arial, helvetica, sans-serif; orphans: 2; widows: 2;”>&nbsp;374.</span></span>

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