101-86-0
Chemical Structure
α-Hexylcinnamaldehyde
- CAS No.: 101-86-0
- Formula:C15H20O
- Molecular Weight:216.32
IUPAC Name: (Z)-2-benzylideneoctanal
InChIKey: GUUHFMWKWLOQMM-QINSGFPZSA-N
SMILES: O=C/C(CCCCCC)=C\C1=CC=CC=C1
Biological Activity: α-Hexylcinnamaldehyde is an O-acetyltransferase (OAT) inhibitor. α-Hexylcinnamaldehyde inhibits OAT-mediated bioactivation of nitroarene mutagens, exerts antimutagenic activity through demutagenic and bioantimutagenic mechanisms, and interferes with ATP-binding cassette (ABC) transporter function to reduce substrate efflux. α-Hexylcinnamaldehyde alters membrane permeability, fluidizes phospholipid membranes, exerts antioxidant effects, and enhances the antiproliferative effect of Doxorubicin on human cancer cells. α-Hexylcinnamaldehyde can be used in the research of colorectal adenocarcinoma, T-cell leukemia, and multidrug-resistant cancers[1][2][3].
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α-Hexylcinnamaldehyde | 92.0% | α-Hexylcinnamaldehyde is an O-acetyltransferase (OAT) inhibitor. α-Hexylcinnamaldehyde inhibits OAT-mediated bioactivation of nitroarene mutagens, exerts antimutagenic activity through demutagenic and bioantimutagenic mechanisms, and interferes with ATP-binding cassette (ABC) transporter function to reduce substrate efflux. α-Hexylcinnamaldehyde alters membrane permeability, fluidizes phospholipid membranes, exerts antioxidant effects, and enhances the antiproliferative effect of Doxorubicin on human cancer cells. α-Hexylcinnamaldehyde can be used in the research of colorectal adenocarcinoma, T-cell leukemia, and multidrug-resistant cancers. | ||||||||||||||||||||
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α-Hexylcinnamaldehyde (Standard) | ≥98% | α-Hexylcinnamaldehyde (Standard) is the analytical standard of α-Hexylcinnamaldehyde. This product is intended for research and analytical applications. α-Hexylcinnamaldehyde is an O-acetyltransferase (OAT) inhibitor. α-Hexylcinnamaldehyde inhibits OAT-mediated bioactivation of nitroarene mutagens, exerts antimutagenic activity through demutagenic and bioantimutagenic mechanisms, and interferes with ATP-binding cassette (ABC) transporter function to reduce substrate efflux. α-Hexylcinnamaldehyde alters membrane permeability, fluidizes phospholipid membranes, exerts antioxidant effects, and enhances the antiproliferative effect of Doxorubicin on human cancer cells. α-Hexylcinnamaldehyde can be used in the research of colorectal adenocarcinoma, T-cell leukemia, and multidrug-resistant cancers. | ||||||||||||||||||||
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Similarity Score 0.74
HY-W751322α-Amylcinnamaldehyde dimethyl acetal -
Similarity Score 0.69
HY-N0964(E)-1-(4-Hydroxyphenyl)dec-1-en-3-one -
Similarity Score 0.68
HY-W014118Sα-Hexylcinnamaldehyde-d5 -
Similarity Score 0.65
HY-W334505Cinnamyl isovalerate -
Similarity Score 0.65
HY-116125Lignarenone B -
Similarity Score 0.64
![(E)-[6]-Dehydroparadol Chemical Structure](//file.medchemexpress.com/product_pic/hy-77293.gif)
HY-77293(E)-[6]-Dehydroparadol -
Similarity Score 0.63
HY-N15453Asperenone -
Similarity Score 0.63
HY-116153HUHS2002 -
Similarity Score 0.63
HY-108919CG-1521 -
Explore the MedChemAI to find more analogs
![(E)-[6]-Dehydroparadol Chemical Structure](http://file.medchemexpress.com/product_pic/hy-77293.gif)
References
- [1]. Di Giacomo S, et al. α-Hexylcinnamaldehyde inhibits the genotoxicity of environmental pollutants in the bacterial reverse mutation assay. J Nat Prod. 2014;77(12):2664-2670. [Content Brief]
- [2]. DI Giacomo S, et al. α-Hexylcinnamaldehyde Synergistically Increases Doxorubicin Cytotoxicity Towards Human Cancer Cell Lines. Anticancer Res. 2016;36(7):3347-3351. [Content Brief]
- [3]. Sarpietro MG, et al. Interaction of α-Hexylcinnamaldehyde with a Biomembrane Model: A Possible MDR Reversal Mechanism. J Nat Prod. 2015;78(5):1154-1159. [Content Brief]
