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Dehydrodiconiferyl alcohol

Dehydrodiconiferyl alcohol Suppliers list
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Products Intro: Product Name:Dehydrodiconiferyl alcohol
CAS:528814-97-3
Purity:98% Package:5mg;10mg;20mg;100mg;1g
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Products Intro: Product Name:Dehydrodiconiferyl alcohol
CAS:528814-97-3
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Products Intro: Product Name:Dehydrodiconiferyl alcohol
CAS:528814-97-3
Purity:HPLC>=95% Package:5mg;10mg;20mg;50mg;100mg;200mg;500mg;1g
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Products Intro: Product Name:Dehydrodiconiferyl alcohol
CAS:528814-97-3
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Products Intro: Product Name:Dehydrodiconiferyl alcohol
CAS:528814-97-3
Purity:HPLC>=95% Package:5mg Remarks:B23381
Dehydrodiconiferyl alcohol Basic information
Product Name:Dehydrodiconiferyl alcohol
Synonyms:3-Benzofuranmethanol, 2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-5-[(1E)-3-hydroxy-1-propen-1-yl]-7-methoxy-;(E)-Dehydrodiconiferyl alcohol
CAS:528814-97-3
MF:C20H22O6
MW:358.39
EINECS:
Product Categories:
Mol File:528814-97-3.mol
Dehydrodiconiferyl alcohol Structure
Dehydrodiconiferyl alcohol Chemical Properties
Boiling point 562.0±50.0 °C(Predicted)
density 1.292±0.06 g/cm3(Predicted)
pka9.79±0.35(Predicted)
Safety Information
MSDS Information
Dehydrodiconiferyl alcohol Usage And Synthesis
Uses(E)-Dehydrodiconiferyl alcohol behaves as good hCA IX and hCA XII dual inhibitors[1]. And (E)-Dehydrodiconiferyl alcohol suppresses the NF-κB nuclear translocation in connective tissue of healing area[2].
DefinitionChEBI: Dehydrodiconiferyl alcohol is a guaiacyl lignin obtained by cyclodimerisation of coniferol. It has a role as a plant metabolite and an anti-inflammatory agent. It is a member of 1-benzofurans, a primary alcohol, a guaiacyl lignin and a member of guaiacols. It is functionally related to a coniferol.
References[1] Costa G, et al. In Silico Identification and Biological Evaluation of Antioxidant Food Components Endowed with IX and XIIhCA Inhibition.Antioxidants (Basel). 2020;9(9):775. Published 2020 Aug 21. DOI:10.3390/antiox9090775
[2] Hu X, et al. Dehydrodiconiferyl alcohol from Silybum marianum (L.) Gaertn accelerates wound healing via inactivating NF-κB pathways in macrophages.J Pharm Pharmacol. 2020;72(2):305-317. DOI:10.1111/jphp.13205
Dehydrodiconiferyl alcohol Preparation Products And Raw materials
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