Dehydrodiconiferyl alcohol MedChemExpress (MCE)

Product Name	dehydrodiconiferyl alcohol
Synonyms	dehydrodiconiferyl alcohol 3-Benzofuranmethanol, 2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-5-(3-hydroxy-1-propen-1-yl)-7-methoxy- (2S)-2,3-Dihydro-2α-(4-hydroxy-3-methoxyphenyl)-5-(3-hydroxy-1-propenyl)-7-methoxy-3β-benzofuranmethanol Synonyms dehydrodiconiferyl alcohol 3-Benzofuranmethanol, 2,3-dihydro-2-(4-hydroxy-3-methoxyphenyl)-5-(3-hydroxy-1-propen-1-yl)-7-methoxy- (2S)-2,3-Dihydro-2α-(4-hydroxy-3-methoxyphenyl)-5-(3-hydroxy-1-propenyl)-7-methoxy-3β-benzofuranmethanol (2S)-2α-(3-Methoxy-4-hydroxyphenyl)-5-(3-hydroxy-1-propenyl)-7-methoxy-2,3-dihydrobenzofuran-3β-methanol (2S)-2α-[4-Hydroxy-3-methoxyphenyl]-2,3-dihydro-5-[(E)-3-hydroxy-1-propenyl]-7-methoxybenzofuran-3β-methanol (2S,3R)-2-(3-Methoxy-4-hydroxyphenyl)-5-[(1E)-3-hydroxy-1-propenyl]-7-methoxy-2,3-dihydrobenzofuran-3-methanol 3-[[(2S)-2α-(3-Methoxy-4-hydroxyphenyl)-3β-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran]-5-yl]-2-propene-1-ol (E)-3-[[(2S)-2α-(3-Methoxy-4-hydroxyphenyl)-3β-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran]-5-yl]-2-propene-1-ol
CAS	4263-87-0
EINECS
Chemical Formula	C20H22O6
Molecular Weight	358.39
inchi
Package	1 mg
Price	Email to quote
Descriptions	Dehydrodiconiferyl alcohol Dehydrodiconiferyl alcohol MedChemExpress (MCE) HY-N2682B 4263-87-0 Please store the product under the recommended conditions in the Certificate of Analysis. Room temperature in continental US Descriptions Dehydrodiconiferyl alcohol Dehydrodiconiferyl alcohol MedChemExpress (MCE) HY-N2682B 4263-87-0 Please store the product under the recommended conditions in the Certificate of Analysis. Room temperature in continental US may vary elsewhere. Dehydrodiconiferyl alcohol is an estrogen receptor agonist that can promote BMP-2-induced osteoblastogenesis. Dehydrodiconiferyl alcohol also exerts anti-inflammatory activity through inactivation of NF-κB pathways. \| \| \| \| \| \| \| \| \| \| [1]. Lee W, et, al. Dehydrodiconiferyl alcohol promotes BMP-2-induced osteoblastogenesis through its agonistic effects on estrogen receptor. Biochem Biophys Res Commun. 2018 Jan 15 495(3):2242-2248. [Content Brief] [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 Feb 72(2):305-317. [Content Brief]
Last Update	2025-04-01 14:45:47

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