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文件

A41208

2-氨基二苯甲酮

Name: 2-氨基二苯甲酮
Brand: ALDRICH

98%

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别名:

2-氨基苯基苯甲酮, 2-氨基苯并苯酮

线性分子式:

H₂NC₆H₄C(O)C₆H₅

CAS号:

2835-77-0

分子量:

197.23

Beilstein:

743425

EC 号:

220-613-9

MDL编号:

MFCD00007713

PubChem化学物质编号:

24890744

NACRES:

NA.22

检测方案

98%

形式

crystals

mp

103-107 °C (lit.)

SMILES string

Nc1ccccc1C(=O)c2ccccc2

InChI

1S/C13H11NO/c14-12-9-5-4-8-11(12)13(15)10-6-2-1-3-7-10/h1-9H,14H2

InChI key

MAOBFOXLCJIFLV-UHFFFAOYSA-N

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储存分类代码

11 - Combustible Solids

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

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Effects of conformational restriction of 2-amino-3-benzoylthiophenes on A(1) adenosine receptor modulation.

Luigi Aurelio et al.

Journal of medicinal chemistry, 53(18), 6550-6559 (2010-09-03)

2-Amino-3-benzoylthiophenes (2A3BTs) have been widely reported to act as allosteric enhancers (AEs) at the A(1) adenosine receptor (A(1)AR). Herein we describe the synthesis of a series of 1-aminoindeno[1,2-c]thiophen-8-ones and a series of (2-aminoindeno[2,1-b]thiophen-3-yl)(phenyl)methanones as conformationally rigid analogues of the 2A3BTs.

Colon-targeted delivery of solubilized bisacodyl by doubly enteric-coated multiple-unit tablet.

Hee J Park et al.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 102, 172-179 (2017-03-11)

A doubly enteric-coated multiple-unit tablet (DET) of bisacodyl (BD) was formulated to selectively deliver the stimulant laxative to the large intestine. Solubilized BD in surfactants was adsorbed into the porous carrier and primarily coated with different combinations of pH-sensitive polymers

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Minakshi Ghate et al.

Luminescence : the journal of biological and chemical luminescence, 33(6), 999-1009 (2018-06-01)

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B-ring-aryl substituted luotonin A analogues with a new binding mode to the topoisomerase 1-DNA complex show enhanced cytotoxic activity.

Víctor González-Ruiz et al.

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Topoisomerase 1 inhibition is an important strategy in targeted cancer chemotherapy. The drugs currently in use acting on this enzyme belong to the family of the camptothecins, and suffer severe limitations because of their low stability, which is associated with

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