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Epifriedelal acetate

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Products Intro: Product Name:EPIFRIEDELANOL ACETATE
CAS:2259-07-6
Purity:95% Package:100g; 1kg Remarks:LN03260921
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Products Intro: Product Name:Epifriedelanol acetate
CAS:2259-07-6
Package:1 mg;5 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
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Products Intro: Product Name:Epifriedelanol acetate
CAS:2259-07-6
Purity:>97.0% Package:5mg Remarks:BBP01635
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Products Intro: Product Name:Epifriedelanolacetate
Purity:98% Package:5mg;10mg;20mg;50mg;100mg;200mg;500mg;1g
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Products Intro: Product Name:Epifriedelanol acetate
CAS:2259-07-6
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Epifriedelal acetate Basic information
Product Name:Epifriedelal acetate
Synonyms:Epifriedelal acetate;24,25,26-Trinoroleanan-3-ol, 5,9,13-trimethyl-, acetate, (3β,4β,5β,8α,9β,10α,13α,14β)-
CAS:2259-07-6
MF:C32H54O2
MW:470.77
EINECS:
Product Categories:
Mol File:2259-07-6.mol
Epifriedelal acetate Structure
Epifriedelal acetate Chemical Properties
Melting point 298 °C(Solvent: Chloroform; Methanol)
Boiling point 461.921±13.00 °C(Press: 760.00 Torr)(predicted)
density 1.010±0.10 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form Powder
Safety Information
MSDS Information
Epifriedelal acetate Usage And Synthesis
DescriptionEpifriedelanol exhibits antibacterial activities. Epifriedelanol and friedelin possess promising antioxidant activity, and they are active against the two cancer cells (human T4 lymphoblastoid (CEM-SS) and human cervical (HeLa) cancer cells) with IC50 values ranging from 3.54 to145 ug/ml. 3. Epifriedelanol can reduce cellular senescence in human primary cells and may be used to develop dietary supplements or cosmetics that modulate tissue aging or aging-associated diseases.
UsesEpifriedelanol acetate (Compound Ⅲc) is a nature product. Epifriedelanol acetate can be isolated from Pachysandra terminalis Sieb[1].
targetAntifection
References[1] Md Afjalus Siraj, et al. Molecular Docking and Molecular Dynamics Simulation Studies of Triterpenes from Vernonia patula with the Cannabinoid Type 1 Receptor. Int J Mol Sci. 12021 Mar 30;22(7):3595 DOI:10.3390/ijms22073595
[2] Kikuchi T, et al. Studies on the neutral constituents of Pachysandra terminalis Sieb, et Zucc. I. Isolation and characterization of sterols and triterpenes. Yakugaku Zasshi. 1969 Oct;89(10):1358-66. Japanese. DOI:10.1248/yakushi1947.89.10_1358
Epifriedelal acetate Preparation Products And Raw materials
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