W431300
检皮素
≥95%
别名:
(2S)-5,7-二羟基-2-(3-羟基-4-甲氧基苯基)-4-苯并二氢吡喃-4-酮, 3′,5,7-三羟基-4′-甲氧基黄酮, 5,7-二羟基-2-(3-羟基-4-甲氧基苯基)-4-苯并二氢吡喃-4-酮
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关于此项目
经验公式（希尔记法）:
C16H14O6
化学文摘社编号:
分子量:
302.28
FEMA Number:
4313
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
16.097
NACRES:
NA.21
MDL number:
Organoleptic:
odorless
Biological source:
synthetic
Food allergen:
no known allergens
产品名称
检皮素, ≥95%
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
InChI key
AIONOLUJZLIMTK-UHFFFAOYSA-N
biological source
synthetic
assay
≥95%
form
powder (with a light tan cast)
mp
227-232 °C
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
odorless
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Disclaimer
用于研发&或非欧盟(EU)食品用途。不用于零售。
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
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
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
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
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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