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SMB01063

Sigma-Aldrich

Kadsurin A

≥90% (LC/MS-ELSD)

Synonym(s):

(2S,3R,3aS,7aR)-2-(1,3-benzodioxol-5-yl)-3a,7a-dimethoxy-3-methyl-5-prop-2-enyl-3,7-dihydro-2H-1-benzofuran-6-one

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About This Item

Empirical Formula (Hill Notation):
C21H24O6
CAS Number:
99340-07-5
Molecular Weight:
372.41
MDL number:
MFCD26406187
UNSPSC Code:
12352205
NACRES:
NA.25

biological source

plant

Assay

≥90% (LC/MS-ELSD)

form

solid

mol wt

372.41

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

SMILES string

O1[C@]2([C@@]([C@@H]([C@H]1c3cc4c(cc3)OCO4)C)(C=C(C(=O)C2)CC=C)OC)OC

InChI

1S/C21H24O6/c1-5-6-15-10-20(23-3)13(2)19(27-21(20,24-4)11-16(15)22)14-7-8-17-18(9-14)26-12-25-17/h5,7-10,13,19H,1,6,11-12H2,2-4H3/t13-,19+,20+,21-/m1/s1

InChI key

YVRYZXAHRGGELT-MZNUGIIHSA-N

General description

Kadsurin A, a furanoid lignan, is a bioacive small molecule commonly found in stems of Kadsura coccinea. This compound exhibits potent biological activity, including anti-inflammatory, anti-paltelet, anti-cancer, and anti-viral properties.

Application

It is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Biochem/physiol Actions

  • Exhibits potent anti-inflammatory properties by inhibiting pro-inflammatory cytokine release from macrophages.
  • Exerts protective effects against muscle injury in vivo and in vitro by effectively suppressing protease and cathepsin activity responsible for muscle tissue degradation.

Features and Benefits

  • High quality compound suitable for multiple research applications
  • Compatible with HPLC and mass spectrometry techniques

Other Notes

For additional information on our range of Biochemicals, please complete this form.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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