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Merck
CN

122351

Sigma-Aldrich

4-二氢色原酮

97%

别名:

2,3-二氢苯并吡喃-4-酮

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About This Item

经验公式(希尔记法):
C9H8O2
CAS号:
分子量:
148.16
Beilstein:
124652
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

形式

solid

折射率

n20/D 1.575 (lit.)

bp

127-128 °C/13 mmHg (lit.)

mp

35-38 °C (lit.)

SMILES字符串

O=C1CCOc2ccccc12

InChI

1S/C9H8O2/c10-8-5-6-11-9-4-2-1-3-7(8)9/h1-4H,5-6H2

InChI key

MSTDXOZUKAQDRL-UHFFFAOYSA-N

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应用

4-色满酮已用于研究从荧光假单胞菌ACB中分离的4-羟基苯乙酮单加氧酶的底物特异性和催化能力

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Zahra Najafi et al.
Bioorganic chemistry, 83, 303-316 (2018-11-06)
A new series of tacrine-coumarin hybrids linked to 1,2,3-triazole were designed, synthesized, and tested as potent dual binding site cholinesterase inhibitors (ChEIs) for the treatment of Alzheimer's disease (AD). Among them, compound 8e was the most potent anti-AChE derivative (IC50 = 27 nM)
Gyeong-Je Lee et al.
Biological & pharmaceutical bulletin, 38(8), 1199-1207 (2015-08-04)
The aim of this study was to examine the anabolic and anticatabolic functions of bavachin in primary rat chondrocytes. With bavachin treatment, chondrocytes survived for 21 d without cell proliferation, and the proteoglycan content and extracellular matrix increased. Short-term monolayer culture
U Thull et al.
Biochemical pharmacology, 47(12), 2307-2310 (1994-06-15)
A number of unsubstituted aromatic hydrocarbons, azaheterocycles, oxaheterocycles and cyclic ketones were screened for their inhibitory potency towards monoamine oxidases (MAO; EC 1.4.3.4.) A and B. Fair activities (IC50 10-100 microM) and selectivities were found for, e.g. naphthalene, anthracene, phenanthrene
G R Harlow et al.
The Journal of biological chemistry, 272(9), 5396-5402 (1997-02-28)
Alanine-scanning mutagenesis was performed on amino acid residues 210-216 of cytochrome P450 3A4, the major drug-metabolizing enzyme of human liver. Mutagenesis of this region, which has been proposed to align with the C-terminal ends of F-helices from cytochromes P450BM-3, P450terp
A R Ibrahim et al.
Journal of natural products, 53(6), 1471-1478 (1990-11-01)
Microbial transformation of chromone, chromanone, and 3 ring A hydroxyflavones (5-hydroxy-, 6-hydroxy-, and 7-hydroxyflavones) was attempted using thirty-two microorganisms. While chromone was not biotransformed, chromanone was transformed to chromone and chromanol by Aspergillus niger in 2% yield. Ring A hydroxylated

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