| Identification | Back Directory | [Name]
Morachalcone A | [CAS]
76472-88-3 | [Synonyms]
Morachalcone A
(2E)-1-[2,4-Dihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-3-(2,4-dihydroxyphenyl)-2-propen-1-one
2-Propen-1-one, 1-[2,4-dihydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-3-(2,4-dihydroxyphenyl)-, (2E)- | [Molecular Formula]
C20H20O5 | [MDL Number]
MFCD20274600 | [MOL File]
76472-88-3.mol | [Molecular Weight]
340.37 |
| Hazard Information | Back Directory | [Description]
Morachalcone A exhibits neuroprotective effects on HT22-immortalized hippocampal cells against glutamate-induced oxidative stress, with EC50 values of 35.5±1 uM.
Morachalcone A exhibits potent inhibitory activity on nitric oxide production in RAW264.7 LPS-activated mouse macrophage cells with IC50 value of 16.4 microM.
3. Morachalcone A displays significant tyrosinase inhibitory activity (IC50, 0.013 uM).
4. Morachalcone A exerts strong pancreatic lipase inhibition with IC 50 value of 6.2 uM. | [Uses]
Morachalcone A is a naturally-occurring aromatase inhibitor (IC50=4.6 mM). Morachalcone A is also a plants metabolite with potential anti-inflammatory and anticancer activity. Morachalcone A inhibits Lipopolysaccharide (HY-D1056)-induced nitric oxide production[1][2][3]. | [Definition]
ChEBI: Morachalcone A is a member of chalcones. | [target]
Tyrosinase | NO | [References]
[1] Brandt D R, et al. The synthetic preparation of naturally-occurring aromatase inhibitors, morachalcone A, isogemichalcone B, and isogemichalcone C[J]. Tetrahedron, 2013, 69(47): 9994-10002.
[2] Kang Y J, et al. Inhibitory effects of morachalcone A on lipopolysaccharide-induced nitric oxide production in raw 264.7 cells[J]. 2009.
[3] Ferlinahayati, et al. Phenolic constituents from the wood of Morus australis with cytotoxic activity. Z Naturforsch C J Biosci. 2008 Jan-Feb;63(1-2):35-9. DOI:10.1515/znc-2008-1-207 |
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