| Identification | Back Directory | [Name]
1,7-Bis(4-hydroxyphenyl)hepta-4,6-dien-3-one | [CAS]
332371-82-1 | [Synonyms]
1,7-BIS(4-HYDROXYPHENYL)HEPTA-4
1,7-Bis(4-hydroxyphenyl)hepta-4,6-dien-3-one
(4E,6E)-1,7-Bis(4-hydroxyphenyl)-4,6-heptadien-3-one
4,6-Heptadien-3-one, 1,7-bis(4-hydroxyphenyl)-, (4E,6E)- | [Molecular Formula]
C19H18O3 | [MOL File]
332371-82-1.mol | [Molecular Weight]
294.34 |
| Hazard Information | Back Directory | [Uses]
1,7-Bis(4-hydroxyphenyl)-hepta-4E,6E-dien-3-one (compound 6) shows antiproliferative activity with ED50s of 57.7, 78.8 μM for 26-L5 and HT-1080 cells, respectively. 1,7-Bis(4-hydroxyphenyl)-hepta-4E,6E-dien-3-one inhibits melanogenesis in B16 melanoma 4A5 cells. 1,7-Bis(4-hydroxyphenyl)-hepta-4E,6E-dien-3-one has the potential for the research of skin disorders[1][2]. | [Definition]
ChEBI: 1,7-bis(4-hydroxyphenyl)hepta-4E-6E-dien-3-one is a diarylheptanoid that is 4E-6E-dien-3-one substituted by 4-hydroxyphenyl group at positions 1 and 7. It has been isolated from the rhizomes of Curcuma kwangsiensis. It has a role as a plant metabolite. It is a diarylheptanoid, a member of phenols and an enone. | [References]
[1] Ali MS, et al. Six new diarylheptanoids from the seeds of Alpinia blepharocalyx. J Nat Prod. 2001 Mar;64(3):289-93. DOI:10.1021/np000496y
[2] Matsumoto T, et al. Diarylheptanoids with inhibitory effects on melanogenesis from the rhizomes of Curcuma comosa in B16 melanoma cells. Bioorg Med Chem Lett. 2013 Sep 15;23(18):5178-81. DOI:10.1016/j.bmcl.2013.07.010 |
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