curcumin and cycloheptanone

curcumin has been researched along with cycloheptanone* in 1 studies

Other Studies

1 other study(ies) available for curcumin and cycloheptanone

Article	Year
Synthesis of curcumin analogues as potential antioxidant, cancer chemopreventive agents. Archiv der Pharmazie, 2004, Volume: 337, Issue:1 New series of 3, 5-bis(substituted benzylidene)-4-piperidones, 2, 7-bis(substituted benzylidene)cycloheptanones, 1, 5-bis(substituted phenyl)-1, 4-pentadien-3-ones, 1, 7-bis(substituted phenyl)-1, 6-heptadien-3, 5-diones, 1, 1-bis(substituted cinnamoyl)-cyclopentanes, and 1, 1-bis(substituted cinnamoyl)cyclohexanes have been synthesized and tested for their antioxidant activity. Among the tested compounds, compounds II(4), II(9) II(10), II(11), V(1), and V(4) exhibited higher free radical scavenger activity with % inhibition values of 90.71, 91.24, 96.91, 94.26, 99.23, and 99.85%, respectively. Moreover, compound V(1) is the safest member toward peripheral multinuclear neutrophils (PMNs) with a % viability value of 91%. Detailed synthesis, spectroscopic, and biological data are reported. Topics: Adenosine Triphosphate; Alkadienes; Animals; Anticarcinogenic Agents; Antioxidants; Cell Survival; Cells, Cultured; Curcumin; Cycloheptanes; Cyclohexanes; Cyclopentanes; Female; Forecasting; Free Radical Scavengers; Free Radicals; Humans; Luminescent Measurements; Male; Molecular Structure; Neutrophils; Piperidones	2004

Article

Year

Synthesis of curcumin analogues as potential antioxidant, cancer chemopreventive agents.

Archiv der Pharmazie, 2004, Volume: 337, Issue:1

New series of 3, 5-bis(substituted benzylidene)-4-piperidones, 2, 7-bis(substituted benzylidene)cycloheptanones, 1, 5-bis(substituted phenyl)-1, 4-pentadien-3-ones, 1, 7-bis(substituted phenyl)-1, 6-heptadien-3, 5-diones, 1, 1-bis(substituted cinnamoyl)-cyclopentanes, and 1, 1-bis(substituted cinnamoyl)cyclohexanes have been synthesized and tested for their antioxidant activity. Among the tested compounds, compounds II(4), II(9) II(10), II(11), V(1), and V(4) exhibited higher free radical scavenger activity with % inhibition values of 90.71, 91.24, 96.91, 94.26, 99.23, and 99.85%, respectively. Moreover, compound V(1) is the safest member toward peripheral multinuclear neutrophils (PMNs) with a % viability value of 91%. Detailed synthesis, spectroscopic, and biological data are reported.

Topics: Adenosine Triphosphate; Alkadienes; Animals; Anticarcinogenic Agents; Antioxidants; Cell Survival; Cells, Cultured; Curcumin; Cycloheptanes; Cyclohexanes; Cyclopentanes; Female; Forecasting; Free Radical Scavengers; Free Radicals; Humans; Luminescent Measurements; Male; Molecular Structure; Neutrophils; Piperidones

2004