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Merck
CN

92996

Kaempferol 7-O-neohesperidoside

≥95.0% (HPLC)

Synonym(s):

3,4′,5,7-Tetrahydroxyflavone 7-[2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranoside], 3,4′,5,7-Tetrahydroxyflavone 7-neohesperidoside

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About This Item

Empirical Formula (Hill Notation):
C27H30O15
CAS Number:
17353-03-6
Molecular Weight:
594.52
NACRES:
NA.25
PubChem Substance ID:
329770190
UNSPSC Code:
12352201
EC Number:
241-377-3
MDL number:
MFCD00017450

Key Documents

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InChI key

ZEJXENDZTYVXDP-CSJHBIPPSA-N

InChI

1S/C27H30O15/c1-9-17(31)20(34)23(37)26(38-9)42-25-21(35)18(32)15(8-28)41-27(25)39-12-6-13(30)16-14(7-12)40-24(22(36)19(16)33)10-2-4-11(29)5-3-10/h2-7,9,15,17-18,20-21,23,25-32,34-37H,8H2,1H3/t9-,15+,17-,18+,20+,21-,23+,25+,26-,27+/m0/s1

SMILES string

O[C@@H]1[C@@H](O[C@@H]2O[C@@H](C)[C@H](O)[C@@H](O)[C@H]2O)[C@H](OC3=CC(OC(C4=CC=C(O)C=C4)=C(O)C5=O)=C5C(O)=C3)O[C@H](CO)[C@H]1O

biological source

seeds (Litchi chinensis)

assay

≥95.0% (HPLC)

form

powder

storage temp.

−20°C

General description

Kaempferol 7-O-neohesperidoside is a flavonoid glycoside that was isolated from the seeds of the Litchi chinensis fruit.

Biochem/physiol Actions

Bioflavonoid, that was shown to have in vitro antitumor activity against cancer cells and might also be involved in the antitumor activity of lychee seeds.
Kaempferol 7-O-neohesperidoside was shown to have anti-proliferative effects on a variety of human cancer cell lines in vitro.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF1707
BCCB2851
BCBT5699
BCBQ8229V
BCBP6121V

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Beatriz Abad-García et al.
Journal of chromatography. A, 1216(28), 5398-5415 (2009-06-09)
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 for the simultaneous identification of phenolic compounds in fruit juices has been
W Nerdal et al.
Acta chemica Scandinavica (Copenhagen, Denmark : 1989), 47(7), 658-662 (1993-07-01)
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. The distance constraints were derived from NOESY NMR spectra. The
Xinya Xu et al.
Journal of agricultural and food chemistry, 59(4), 1205-1209 (2011-02-04)
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 chromatography and high-performance liquid chromatography (HPLC) preparation. They were identified

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