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安全信息

419753

Sigma-Aldrich

7-羟基黄烷酮

98%

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别名:
7-羟基-2-苯基苯并二氢吡喃-4-酮
经验公式（希尔记法）:
C15H12O3
CAS号:
6515-36-2
分子量:
240.25
MDL编号:
MFCD00017487
PubChem化学物质编号:
24866274
NACRES:
NA.22

检测方案

98%

形式

solid

mp

188-190 °C (lit.)

SMILES string

Oc1ccc2C(=O)CC(Oc2c1)c3ccccc3

InChI

1S/C15H12O3/c16-11-6-7-12-13(17)9-14(18-15(12)8-11)10-4-2-1-3-5-10/h1-8,14,16H,9H2

InChI key

SWAJPHCXKPCPQZ-UHFFFAOYSA-N

Gene Information

mouse ... Maoa(17161)
rat ... Aldh1a2(116676)

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相关类别

应用

7-Hydroxyflavanone has been used for the stereoisomeric separation of flavonoids using polysaccharide-based chiral stationary phases by nano-liquid chromatography (nano-LC).

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H315 - H319 - H335

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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F R Cross
Journal of cell science. Supplement, 12, 117-127 (1989-01-01)
The DAF1-1 mutation reduces cell size and reduces or eliminates G1 phase in Saccharomyces cerevisiae, and results in alpha-factor resistance. DAF1-1 cells transferred into low cycloheximide express an increased G1 phase in their cycle, suggesting that G1 regulation is present
Tomasz Wróblewski et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 215, 81-87 (2019-03-02)
In this work the photophysical properties of 7-hydroxyflavanone in acetonitrile, ethanol and methanol have been studied. The quantum chemical calculations as well as the experimental measurements have been performed. The absorption and emission spectra have been obtained for 7-hydroxyflavanone dissolved
Přemysl Mladěnka et al.
Journal of inorganic biochemistry, 105(5), 693-701 (2011-04-01)
Flavonoids have been demonstrated to possess miscellaneous health benefits which are, at least partly, associated with iron chelation. In this in vitro study, 26 flavonoids from different subclasses were analyzed for their iron chelating activity and stability of the formed
[Microbial kinetics: experiences with Staphylococcus aureus ATCC 25 293 and bacteriostatic drugs].
N B Pappano et al.
Revista latinoamericana de microbiologia, 29(4), 367-372 (1987-10-01)
Julie Rakel Mikell et al.
Chemical & pharmaceutical bulletin, 60(9), 1139-1145 (2012-09-15)
Microbial metabolism of 7-hydroxyflavanone (1) with fungal culture Cunninghamella blakesleeana (ATCC 8688a), yielded flavanone 7-sulfate (2), 7,4'-dihydroxyflavanone (3), 6,7-dihydroxyflavanone (4), 6-hydroxyflavanone 7-sulfate (5), and 7-hydroxyflavanone 6-sulfate (6). Mortierella zonata (ATCC 13309) also transformed 1 to metabolites 2 and 3 as
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