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inulicin

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inulicin Basic information

Product Name:
inulicin
Synonyms:
  • (3aS)-3,3aα,4,5,8,8aα-Hexahydro-4α-hydroxy-6-(3-acetoxypropyl)-5α,7-dimethyl-3-methylene-2H-cyclohepta[b]furan-2-one
  • (3aS)-6-(3-Acetoxypropyl)-3,3aα,4,5,8,8aα-hexahydro-4α-hydroxy-5α,7-dimethyl-3-methylene-2H-cyclohepta[b]furan-2-one
  • Britannilactone
  • (3aS,4S,7aR)-5-[(1S)-4-(Acetyloxy)-1-methylbutyl]-3a,4,7,7a-tetrahydro-4-hydroxy-6-methyl-3-methylene-2(3H)-benzofuranone
  • inulicin
  • 6-(3-acetoxy-propyl)-4-hydroxy-5,7-dimethyl-3-methylene-3,3a,4,5,8,8a-hexahydro-cyclohepta[b]furan-2-one
  • 1-O-Acetylbritannilactone (Inulicin)
  • 2(3H)-Benzofuranone,5-[(1S)-4-(acetyloxy)-1-methylbutyl]-3a,4,7,7a-tetrahydro-4-hydroxy-6-methyl-3-methylene-,(3aS,4S,7aR)-
CAS:
33627-41-7
MF:
C17H24O5
MW:
308.37
Mol File:
33627-41-7.mol
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inulicin Chemical Properties

Melting point:
124.0-126.1 °C
Boiling point:
481.7±45.0 °C(Predicted)
Density 
1.16
storage temp. 
4°C, protect from light
solubility 
DMSO: soluble
form 
A solid
pka
13.71±0.60(Predicted)
color 
White to off-white
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inulicin Usage And Synthesis

Biological Activity

Inulicin (1-O-Acetylbritannilactone) is an active compound isolated from Inula Britannica L. It inhibits VEGF-mediated activation of Src and FAK. It also inhibits LPS-induced PGE2 production and COX-2 expression, as well as NF-κB activation and translocation.

in vivo

Administration of a single dose of Inulicin (1-O-Acetylbritannilactone; 12 mg/kg/day) remarkably suppresses growth of A549 xenografts in nude mice. In vivo microvessels formation and Src activation are also significantly inhibited in Inulicin-treated xenograft tumors. To investigate the potential activity of Inulicin in vivo, a nude mice xenograft model is applied.

target

NF-κB

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COX-2

inulicinSupplier

BioBioPha Co., Ltd.
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18302802153 18981717076
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