Xanthoangelol

Modify Date: 2025-08-25 14:06:04

Xanthoangelol structure	Common Name	Xanthoangelol
	CAS Number	62949-76-2	Molecular Weight	392.48700
	Density	1.165g/cm3	Boiling Point	605.8ºC at 760 mmHg
	Molecular Formula	C₂₅H₂₈O₄	Melting Point	N/A
	MSDS	N/A	Flash Point	334.2ºC

Use of Xanthoangelol

Xanthoangelol, extracted from Angelica keiskei, suppresses obesity-induced inflammatory responses. Xanthoangelol possesses antibacterial activity[1][2]. Xanthoangelol and inhibits monoamine oxidases[3]. Xanthoangelol induces apoptosis in neuroblastoma and leukemia cells[4].

Name	(E)-1-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one
Synonym	More Synonyms

Description	Xanthoangelol, extracted from Angelica keiskei, suppresses obesity-induced inflammatory responses. Xanthoangelol possesses antibacterial activity[1][2]. Xanthoangelol and inhibits monoamine oxidases[3]. Xanthoangelol induces apoptosis in neuroblastoma and leukemia cells[4].
Related Catalog	Signaling Pathways >> Apoptosis >> Apoptosis Signaling Pathways >> Epigenetics >> AMPK Research Areas >> Cancer Research Areas >> Infection Signaling Pathways >> PI3K/Akt/mTOR >> AMPK Signaling Pathways >> Anti-infection >> Bacterial
References	[1]. Li Y, et al. Xanthoangelol and 4-hydroxyderrcin suppress obesity-induced inflammatory responses. Obesity (Silver Spring). 2016 Nov;24(11):2351-2360. [2]. Inamori Y, et al. Antibacterial activity of two chalcones, xanthoangelol and 4-hydroxyderricin, isolated from the root of Angelica keiskei KOIDZUMI. Chem Pharm Bull (Tokyo). 1991 Jun;39(6):1604-5. [3]. Kim JH, et al. Xanthoangelol and 4-Hydroxyderricin Are the Major Active Principles of the Inhibitory Activities against Monoamine Oxidases on Angelica keiskei K. Biomol Ther (Seoul). 2013 May 30;21(3):234-40. [4]. Keiichi TABATA, et al. Xanthoangelol, a Major Chalcone Constituent of Angelica keiskei, Induces Apoptosis in Neuroblastoma and Leukemia Cells. Biol. Pharm. Bull. 28(8) 1404-1407 (2005).

Description

Related Catalog

Signaling Pathways >> Apoptosis >> Apoptosis

Signaling Pathways >> Epigenetics >> AMPK

Research Areas >> Cancer

Research Areas >> Infection

Signaling Pathways >> PI3K/Akt/mTOR >> AMPK

Signaling Pathways >> Anti-infection >> Bacterial

References

[1]. Li Y, et al. Xanthoangelol and 4-hydroxyderrcin suppress obesity-induced inflammatory responses. Obesity (Silver Spring). 2016 Nov;24(11):2351-2360.

[2]. Inamori Y, et al. Antibacterial activity of two chalcones, xanthoangelol and 4-hydroxyderricin, isolated from the root of Angelica keiskei KOIDZUMI. Chem Pharm Bull (Tokyo). 1991 Jun;39(6):1604-5.

[3]. Kim JH, et al. Xanthoangelol and 4-Hydroxyderricin Are the Major Active Principles of the Inhibitory Activities against Monoamine Oxidases on Angelica keiskei K. Biomol Ther (Seoul). 2013 May 30;21(3):234-40.

[4]. Keiichi TABATA, et al. Xanthoangelol, a Major Chalcone Constituent of Angelica keiskei, Induces Apoptosis in Neuroblastoma and Leukemia Cells. Biol. Pharm. Bull. 28(8) 1404-1407 (2005).

Density	1.165g/cm3
Boiling Point	605.8ºC at 760 mmHg
Molecular Formula	C₂₅H₂₈O₄
Molecular Weight	392.48700
Flash Point	334.2ºC
Exact Mass	392.19900
PSA	77.76000
LogP	5.93470
Index of Refraction	1.625

Xanthoangelol

xanthoangerol

2',4,4'-trihydroxy-3'-geranylchalcone

3-geranyl-2,4,4'-trihydroxychalcone

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Xanthoangelol

Use of Xanthoangelol

Names

Xanthoangelol Biological Activity

Chemical & Physical Properties

Synthetic Route

Synonyms

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.