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Merck

92996

Sigma-Aldrich

Kampferöl 7-O-Neohesperidosid

≥95.0% (HPLC)

Synonym(e):

3,4′,5,7-Tetrahydroxyflavon-7-[2-O-(6-deoxy-α-L-mannopyranosyl)-β-D-glucopyranosid], 3,4′,5,7-Tetrahydroxyflavon-7-neohesperidosid

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About This Item

Empirische Formel (Hill-System):
C27H30O15
CAS-Nummer:
Molekulargewicht:
594.52
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352201
PubChem Substanz-ID:
NACRES:
NA.25

Biologische Quelle

seeds (Litchi chinensis)

Assay

≥95.0% (HPLC)

Form

powder

Lagertemp.

−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

InChIKey

ZEJXENDZTYVXDP-CSJHBIPPSA-N

Allgemeine Beschreibung

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

Biochem./physiol. Wirkung

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.

Verpackung

Bottomless glass bottle. Contents are inside inserted fused cone.

Sonstige Hinweise

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

Lagerklassenschlüssel

13 - Non Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

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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