7-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-3,5-dihydroxy-2-(4-hydroxyphenyl)-4H-benzopyran-4-one

Modify Date: 2025-08-25 13:08:23

7-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-3,5-dihydroxy-2-(4-hydroxyphenyl)-4H-benzopyran-4-one structure	Common Name	7-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-3,5-dihydroxy-2-(4-hydroxyphenyl)-4H-benzopyran-4-one
	CAS Number	17353-03-6	Molecular Weight	594.51800
	Density	1.76g/cm3	Boiling Point	934.7ºC at 760mmHg
	Molecular Formula	C₂₇H₃₀O₁₅	Melting Point	N/A
	MSDS	Chinese USA	Flash Point	310.4ºC

Use of 7-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-3,5-dihydroxy-2-(4-hydroxyphenyl)-4H-benzopyran-4-one

Kaempferol 7-O-neohesperidoside is a ?avonoid glycoside that can be isolated from Litchi chinensis. Kaempferol 7-O-neohesperidoside exhibits significant cytotoxic activity against A549, LAC, Hep-G2, and HeLa cell lines with IC50s of 0.53, 7.93, 0.020, and 0.051 μM, respectively[1].

Name	7-[[2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]-3,5-dihydroxy-2-(4-hydroxyphenyl)-4H-benzopyran-4-one
Synonym	More Synonyms

Description	Kaempferol 7-O-neohesperidoside is a ?avonoid glycoside that can be isolated from Litchi chinensis. Kaempferol 7-O-neohesperidoside exhibits significant cytotoxic activity against A549, LAC, Hep-G2, and HeLa cell lines with IC50s of 0.53, 7.93, 0.020, and 0.051 μM, respectively[1].
Related Catalog	Research Areas >> Cancer Signaling Pathways >> Others >> Others
References	[1]. Xu X, et al. Flavonoid Glycosides from the Seeds of Litchi chinensis. J Agric Food Chem. 2011 Feb 23;59(4):1205-9.

Density	1.76g/cm3
Boiling Point	934.7ºC at 760mmHg
Molecular Formula	C₂₇H₃₀O₁₅
Molecular Weight	594.51800
Flash Point	310.4ºC
Exact Mass	594.15800
PSA	249.20000
Vapour Pressure	0mmHg at 25°C
Index of Refraction	1.744
Storage condition	20°C

MSDS(Chinese)

RIDADR	NONH for all modes of transport

Naringin

CAS#:10236-47-2

7-[[2-O-(6-deox...

CAS#:17353-03-6

Literature: Phytochemistry (Elsevier), , vol. 20, p. 297 - 304

Precursor 1
CAS#:10236-47-2 Naringin
DownStream 0

Flavonoid Glycosides from the Seeds of Litchi chinensis.

J. Agric. Food Chem. 59 , 1205-1209, (2011)

Seven flavonoid glycosides, including one new (1) and five previously uncharacterized (3-7), were obtained from the seeds of lychee ( Litchi chinensis Sonn. cv. Heiye) by means of repetitive column ch...

A general analytical strategy for the characterization of phenolic compounds in fruit juices by high-performance liquid chromatography with diode array detection coupled to electrospray ionization and triple quadrupole mass spectrometry.

J. Chromatogr. A. 1216 , 5398-5415, (2009)

In the present study, a methodology based on liquid chromatography with diode array detection (HPLC/DAD) coupled to an electrospray ionization (ESI) interface and a triple quadrupole mass spectrometer...

NMR studies of a plant flavonoid--DNA oligonucleotide complex.

Acta Chem. Scand. 47(7) , 658-62, (1993)

A structural model of the solution complex between a flavonoid and a DNA dodecamer containing the E. coli wild-type lac promoter sequence (TATGTT) was obtained using simulated annealing for refinement...

4'-O-Methylkaempferol

3,5,4'-trihydroxy-7-methoxyflavanone

4'-Methoxy-3,5,7-trihydroxyflavone

Kaempferide

Kaempferid

kaempferol 4'-methyl ether

Kaempferol 7-O-neohesperidoside

kaempferol 7-neohesperidoside

4'-Methylkaempferol

kaempferol 7-O-neohesperidoside

3,5,7-trihydroxy-4'-methoxyflavone

kaempferol 7-neohsperidoside

5,7-dihydroxy-4'-methoxyflavonol

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7-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-3,5-dihydroxy-2-(4-hydroxyphenyl)-4H-benzopyran-4-one

Use of 7-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-3,5-dihydroxy-2-(4-hydroxyphenyl)-4H-benzopyran-4-one

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Biological Activity

Chemical & Physical Properties

MSDS

Safety Information

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Precursor & DownStream

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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.