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Merck

92996

Sigma-Aldrich

Kaempferol 7-O-neohesperidoside

≥95.0% (HPLC)

Sinónimos:

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

Fórmula empírica (notación de Hill):
C27H30O15
Número de CAS:
Peso molecular:
594.52
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25

biological source

seeds (Litchi chinensis)

assay

≥95.0% (HPLC)

form

powder

storage temp.

−20°C

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

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

InChI key

ZEJXENDZTYVXDP-CSJHBIPPSA-N

General description

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

Biochem/physiol Actions

Kaempferol 7-O-neohesperidoside was shown to have anti-proliferative effects on a variety of human cancer cell lines in vitro.
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.

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

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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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