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| | 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 Chemical Properties |
| Boiling point | 562.0±50.0 °C(Predicted) | | density | 1.292±0.06 g/cm3(Predicted) | | pka | 9.79±0.35(Predicted) |
| | 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]. | | Definition | ChEBI: 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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