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Details

Stereochemistry ACHIRAL
Molecular Formula C9H12O3
Molecular Weight 168.1898
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HOMOVANILLYL ALCOHOL

SMILES

COC1=CC(CCO)=CC=C1O

InChI

InChIKey=XHUBSJRBOQIZNI-UHFFFAOYSA-N
InChI=1S/C9H12O3/c1-12-9-6-7(4-5-10)2-3-8(9)11/h2-3,6,10-11H,4-5H2,1H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Inhibitory effects of Zingiber officinale Roscoe derived components on aldose reductase activity in vitro and in vivo.
2006 Sep 6
Convenient synthesis of hydroxytyrosol and its lipophilic derivatives from tyrosol or homovanillyl alcohol.
2008 Oct 8
Protective effect of hydroxytyrosol and its metabolite homovanillic alcohol on H(2)O(2) induced lipid peroxidation in renal tubular epithelial cells.
2008 Sep
Human absorption of a supplement containing purified hydroxytyrosol, a natural antioxidant from olive oil, and evidence for its transient association with low-density lipoproteins.
2010 Apr
Involvement of ERK, Akt and JNK signalling in H2O2-induced cell injury and protection by hydroxytyrosol and its metabolite homovanillic alcohol.
2010 Jun
Simultaneous quantification of oleuropein and its metabolites in rat plasma by liquid chromatography electrospray ionization tandem mass spectrometry.
2010 May
Protective effect of simple phenols from extravirgin olive oil against lipid peroxidation in intestinal Caco-2 cells.
2010 Oct
Patents
Name Type Language
HOMOVANILLYL ALCOHOL
Systematic Name English
MOPET
Common Name English
3-METHOXY-4-HYDROXYPHENYLETHANOL
Systematic Name English
4-(2-HYDROXYETHYL)-2-METHOXYPHENOL
Systematic Name English
Code System Code Type Description
PUBCHEM
16928
Created by admin on Fri Dec 15 19:46:43 GMT 2023 , Edited by admin on Fri Dec 15 19:46:43 GMT 2023
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WIKIPEDIA
HOMOVANILLYL ALCOHOL
Created by admin on Fri Dec 15 19:46:43 GMT 2023 , Edited by admin on Fri Dec 15 19:46:43 GMT 2023
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EPA CompTox
DTXSID40178494
Created by admin on Fri Dec 15 19:46:43 GMT 2023 , Edited by admin on Fri Dec 15 19:46:43 GMT 2023
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FDA UNII
9A7EE8MS6A
Created by admin on Fri Dec 15 19:46:43 GMT 2023 , Edited by admin on Fri Dec 15 19:46:43 GMT 2023
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CAS
2380-78-1
Created by admin on Fri Dec 15 19:46:43 GMT 2023 , Edited by admin on Fri Dec 15 19:46:43 GMT 2023
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ECHA (EC/EINECS)
219-175-1
Created by admin on Fri Dec 15 19:46:43 GMT 2023 , Edited by admin on Fri Dec 15 19:46:43 GMT 2023
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