Name | 1,7-Bis(4-hydroxy-3-methoxyphenyl)-3,5-heptanediol |
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Synonyms |
1,7-Bis(4-hydroxy-3-methoxyphenyl)heptane-3,5-diol
Curcumin bis-acetate octahydrocurcumin Curcumin 4,4'-diacetate 1,6-Heptadiene-3,5-dione,1,7-bis(4-(acetyloxy)-3-methoxyphenyl) 1,7-bis(4-acetoxy-3-methoxyphenyl)hepta-1,6-diene-3,5-dione hexahydrocurcuminol diacetyldiferuloylmethane diacetylcurcumin 3,5-Heptanediol, 1,7-bis(4-hydroxy-3-methoxyphenyl)- 1,7-Bis(4-hydroxy-3-methoxyphenyl)-3,5-heptanediol curcumin acetic acid ester (diacetylated) 1,7-bis(4-acetoxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione 4,4'-Diacetylcurcumin Di-O-Acetylcurcumin Acetic acid,4-[7-(4-acetoxy-3-methoxy-phenyl)-3,5-dioxo-hepta-1,6-dienyl]-2-methoxy-phenyl ester 1,7-bis-(4-hydroxy-3-methoxyphenyl)heptane-3,5-dione |
Description | Octahydrocurcumin is a hydrogenated derivatives of curcumin; metabolite of curcumin.IC50 value:Target: OKT3-induced PBMC proliferation was inhibited by octahydrocurcumin with IC50 of 82 uM. The investigated substances with the strongest effect on radical scavenging were tetrahydro-, hexahydro-, and octahydrocurcumin with IC50 values of 10.0, 11.7, and 12.3 microM, respectively [1]. curcumin and tetrahydrocurcumin significantly inhibited the release of prominent cytokines, including tumor necrosis factor?α (TNF?α) and interleukin?6 (IL?6); however, hexahydrocurcumin and octahydrocurcumin did not significantly alter cytokine release [2]. Hydrogenated derivatives of curcumin exhibited stronger DPPH scavenging activity compared to curcumin and a reference antioxidant, trolox. The scavenging activity significantly decreased in the order THC>HHC=OHC>trolox>curcumin>Dmc>>>Bdmc [3]. |
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Related Catalog | |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 623.5±55.0 °C at 760 mmHg |
Molecular Formula | C21H28O6 |
Molecular Weight | 376.443 |
Flash Point | 330.9±31.5 °C |
Exact Mass | 376.188599 |
PSA | 99.38000 |
LogP | 1.73 |
Vapour Pressure | 0.0±1.9 mmHg at 25°C |
Index of Refraction | 1.592 |
Storage condition | -20°C |