| Weight | 372.417 g/mol |
|---|---|
| Formula | C21H24O6 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 10 |
Tetrahydrocurcumin (36062-04-1)
Score:
#1823 in Biochemistry
,
#3963 in Biology
,
#4988 in Chemistry
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- Curcumin, demethoxycurcumin, bisdemethoxycurcumin, tetrahydrocurcumin and turmerones differentially regulate anti-inflammatory and anti-proliferative responses through a ROS-independent mechanism (Carcinogenesis, 2007)
- Involvement of the -diketone moiety in the antioxidative mechanism of tetrahydrocurcumin (Biochemical Pharmacology, 1996)
- Curcumin and especially tetrahydrocurcumin ameliorate oxidative stress-induced renal injury in mice. (Journal of Nutrition, 2001)
- Validated LC/MS/MS assay for curcumin and tetrahydrocurcumin in rat plasma and application to pharmacokinetic study of phospholipid complex of curcumin. (Journal of Pharmaceutical and Biomedical Analysis, 2006)
- Effects of curcumin, demethoxycurcumin, bisdemethoxycurcumin and tetrahydrocurcumin on 12-O-tetradecanoylphorbol-13-acetateinduced tumor promotion (Carcinogenesis, 1995)
- Modulation of function of three ABC drug transporters, P-glycoprotein (ABCB1), mitoxantrone resistance protein (ABCG2) and multidrug resistance protein 1 (ABCC1) by tetrahydrocurcumin, a major metabolite of curcumin (Molecular and Cellular Biochemistry, 2007)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=C(C=CC(=C1)CCC(=O)CC(=O)CCC2=CC(=C(C=C2)O)OC)O
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InChIKeyLBTVHXHERHESKG-UHFFFAOYSA-N
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Synthesis
Guaiacol
+
Reactant
(Friedel-Crafts alkylation)
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methyl 2-(3,4-dimethoxyphenyl)acetate
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Tetrahydrocurcumin
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