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W431300

Sigma-Aldrich

Hesperetin

≥95%

Synonym(e):

(2S)-5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-chromanon, 3′,5,7-Trihydroxy-4′,-methoxyflavanon, 5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-chromanon

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About This Item

Empirische Formel (Hill-System):
C16H14O6
CAS-Nummer:
69097-99-0
Molekulargewicht:
302.28
FEMA-Nummer:
4313
MDL-Nummer:
MFCD00016956
UNSPSC-Code:
12164502
PubChem Substanz-ID:
329830698
Flavis-Nummer:
16.097
NACRES:
NA.21

Biologische Quelle

synthetic

Qualitätsniveau

400

Assay

≥95%

Form

powder (with a light tan cast)

mp (Schmelzpunkt)

227-232 °C

Anwendung(en)

flavors and fragrances

Dokumentation

see Safety & Documentation for available documents

Nahrungsmittelallergen

no known allergens

Organoleptisch

odorless

SMILES String

COc1ccc(cc1O)C2CC(=O)c3c(O)cc(O)cc3O2

InChI

1S/C16H14O6/c1-21-13-3-2-8(4-10(13)18)14-7-12(20)16-11(19)5-9(17)6-15(16)22-14/h2-6,14,17-19H,7H2,1H3

InChIKey

AIONOLUJZLIMTK-UHFFFAOYSA-N

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Haftungsausschluss

For R&D or non-EU Food use. Not for retail sale.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
SHBS4383
SHBQ3423
SHBP4420
SHBN0365
SHBL8821

Die passende Version wird nicht angezeigt?

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Hesperidin Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1794

Hesperidin

Eriodictyol ≥95.0% (HPLC)

Sigma-Aldrich

94258

Eriodictyol

Tangeretin ≥95% (HPLC)

Sigma-Aldrich

T8951

Tangeretin

Narirutin phyproof® Reference Substance

PHL83339

Narirutin

Naringenin-6-C-glucoside ≥95% (LC/MS-ELSD)

Sigma-Aldrich

SMB00137

Naringenin-6-C-glucoside

Naringin ≥90% (HPLC), from citrus fruit

Sigma-Aldrich

N1376

Naringin

Naringin ≥95% (HPLC)

Sigma-Aldrich

71162

Naringin

Sinensetin ≥98% (HPLC)

Sigma-Aldrich

SML1787

Sinensetin

Apigenin ≥97% (TLC), from citrus

Sigma-Aldrich

SMB00702

Apigenin

Ramesh Elango et al.
Journal of Asian natural products research, 20(6), 559-569 (2017-05-26)
We studied the chemoprevention property of hesperetin on H522 cells using MTT, an apoptosis assay, an analysis of cell cycle progression, and the mitochondrial membrane potential, and apoptotic marker gene expression was determined using quantitative PCR. Hesperetin enhanced apoptotic cell
Elena Valeria Fuior et al.
Pharmaceutics, 11(8) (2019-08-07)
Citrus flavonoids have well-documented protective effects on cardiovascular system, but the poor water solubility and reduced bioavailability restrict their therapeutic use. We aimed to overcome these limitations and encapsulated naringenin and hesperetin into lipid nanoemulsions (LNs), targeted to vascular cell
Chuye Ji et al.
International journal of biological macromolecules, 168, 775-783 (2020-11-24)
The interaction between biomacromolecules and ligands has attracted great interest because of their biological properties. Calf thymus DNA (ctDNA) can interact with bioactive compounds to form complexes. Here, ctDNA-ligand complexes were studied using fluorescence, absorption, and infrared spectroscopy, circular dichroism
Xuan Zeng et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 1136, 121846-121846 (2019-12-11)
Naringin has been documented to possess multiple pharmacological activities. Reported pharmacokinetic studies revealed that oral bioavailability of naringin was low, in contrast to its significant pharmacological effects. The in vivo distribution of naringin and derived metabolites might partly explain this
Weixin Wang et al.
Journal of agricultural and food chemistry, 63(43), 9488-9495 (2015-10-13)
The objective of this study was to investigate the ability of resveratrol and hesperetin to scavenge acrolein at pH 7.4 and 37 °C. About 6.4 or 5.2% of acrolein remained after reaction with resveratrol or hesperetin for 12 h at
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