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122351

4-二氢色原酮

Name: 4-二氢色原酮
Brand: ALDRICH

97%

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别名:

2,3-二氢苯并吡喃-4-酮

经验公式（希尔记法）:

C₉H₈O₂

CAS号:

491-37-2

分子量:

148.16

Beilstein:

124652

EC 号:

207-736-3

MDL编号:

MFCD00006840

PubChem化学物质编号:

24847484

NACRES:

NA.22

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 string

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。

储存分类代码

11 - Combustible Solids

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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示例

T1503

货号

25G

包装规格/数量

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705578-5MG-PW

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MMYOMAG-74K-13

1000309185

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Screening of unsubstituted cyclic compounds as inhibitors of monoamine oxidases.

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

Alanine-scanning mutagenesis of a putative substrate recognition site in human cytochrome P450 3A4. Role of residues 210 and 211 in flavonoid activation and substrate specificity.

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

Biological Effects of the Herbal Plant-Derived Phytoestrogen Bavachin in Primary Rat Chondrocytes.

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

Novel tacrine-coumarin hybrids linked to 1,2,3-triazole as anti-Alzheimer's compounds: In vitro and in vivo biological evaluation and docking study.

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)

Interaction of Arylidenechromanone/Flavanone Derivatives with Biological Macromolecules Studied as Human Serum Albumin Binding, Cytotoxic Effect, Biocompatibility Towards Red Blood Cells.

Angelika A Adamus-Grabicka et al.

Molecules (Basel, Switzerland), 23(12) (2018-12-06)

The aim of this study was to determine the cytotoxic effect of 3-arylidenechromanone (1) and 3arylideneflavanone (2) on HL-60 and NALM-6 cell lines (two human leukemia cell lines) and a WM-115 melanoma cell line. Both compounds exhibited high cytotoxic activity

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