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3-O-trans-p-CouMaroyltorMentic acid

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3-O-trans-p-CouMaroyltorMentic acid Basic information

Product Name:
3-O-trans-p-CouMaroyltorMentic acid
Synonyms:
  • 3-O-trans-p-CouMaroyltorMentic acid
  • 3-O-p-CouMaroyltorMentic acid
  • Urs-12-en-28-oic acid, 2,19-dihydroxy-3-[[(2E)-3-(4-hydroxyphenyl)-1-oxo-2-propenyl]oxy]-, (2α,3β)-
  • 3-O-trans-p-Coumaroyltormenticaci
CAS:
121064-78-6
MF:
C39H54O7
MW:
634.85
Mol File:
121064-78-6.mol
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3-O-trans-p-CouMaroyltorMentic acid Chemical Properties

Melting point:
245-247 °C(Solv: methanol (67-56-1))
Boiling point:
745.5±60.0 °C(Predicted)
Density 
1.23±0.1 g/cm3(Predicted)
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
Powder
pka
4.45±0.70(Predicted)
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3-O-trans-p-CouMaroyltorMentic acid Usage And Synthesis

Description

3-O-(E)-p-coumaroyl tormentic acid induces apoptotic cell death in human leukemia (HL60) via mainly mitochondrial pathway by, at least in part, Topo I inhibition, it may be promising lead compound for developing an effective drug for treatment of leukemia. 3-O-trans-p-coumaroyltormentic acid shows cytotoxicity against four human tumor cell lines (A549, SK-OV-3, SK-MEL-2, and HCT-15) in vitro, the IC50 values of 13.72, 14.29,14.61, 14.04 uM, respectively. 3. 3beta-O-cis-p-Coumaroyltormentic acid, and 3beta-O-trans-p-coumaroyltormentic acid are weakly selective for vancomycin-resistant Enterococcus (VRE) compared with eukaryotic cells, with an MIC of 59.4microg/mL and a 50% inhibitory concentration (IC50) of 70microg/mL for monkey kidney epithelial (MA104) cells. 4. A mixture of 3-O-cis-p-coumaroyltormentic acid and 3-O-trans-p-coumaroyltormentic acid shows an inhibitory effect comparable to (-)-epigallocatechin gallate (EGCG) of green tea on the activation of Epstein-Barr virus early antigen (EBV-EA) induced by 12-O-tetradeca--noylphorbol-13-acetate (TPA).

Definition

ChEBI: 3-O-trans-p-coumaroyltormentic acid is a triterpenoid. It has a role as a metabolite.

target

Antifection | Caspase

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