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Merck
CN

264938

Sigma-Aldrich

1-甲基异喹啉

97%

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About This Item

经验公式(希尔记法):
C10H9N
CAS号:
分子量:
143.19
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

97%

表单

liquid

折射率

n20/D 1.6140 (lit.)

沸点

126-128 °C/16 mmHg (lit.)

密度

1.078 g/mL at 25 °C (lit.)

SMILES字符串

Cc1nccc2ccccc12

InChI

1S/C10H9N/c1-8-10-5-3-2-4-9(10)6-7-11-8/h2-7H,1H3

InChI key

PBYMYAJONQZORL-UHFFFAOYSA-N

基因信息

human ... CYP2A6(1548)
mouse ... Cyp2a5(13087)

注意

低熔点固体

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

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

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

新产品

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分析证书(COA)

Lot/Batch Number

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T Aiuchi et al.
Neurochemistry international, 28(3), 319-323 (1996-03-01)
The effect of 1-methyl-isoquinoline (MIQ+) on the respiratory inhibition and the uptake of MIQ+ were measured using mouse liver mitochondria. MIQ+ inhibited the electron transport of complex I but did not inhibit the respiration of mitochondria with succinate as a
Koichi Mitsukura et al.
Journal of bioscience and bioengineering, 115(6), 651-653 (2013-01-08)
Verticillium sp. GF39, catalyzing the oxidation of 1-methylisoquinoline to 1-methylisoquinoline N-oxide, was found to be the highest N-oxide producer. Under the optimized reaction conditions, the whole cells of Verticillium sp. GF39 formed 5 mM 1-methylisoquinoline N-oxide from 1-methylisoquinoline with a molar
Reactivity of 1-methylisoquinoline. Synthesis of 2-(1-isoquinolinemethylidene)-1, 3, 4-thiadiazole derivatives.
Abdallah TA, et al.
Phosphorus, Sulfur, and Silicon and the Related Elements, 177(1), 59-66 (2002)
Kunal Roy et al.
European journal of medicinal chemistry, 44(5), 1941-1951 (2008-12-27)
A series of naphthalene and non-naphthalene derivatives (n=42) having cytochrome P450 2A6 and 2A5 inhibitory activities, reported by Rahnasto et al., were subjected to QSAR and QAAR studies. The analyses were performed using electronic, spatial, shape and thermodynamic descriptors to
Minna Rahnasto et al.
Journal of medicinal chemistry, 48(2), 440-449 (2005-01-22)
The purpose of this study was to develop screening and in silico modeling methods to obtain accurate information on the active center of CYP2A6, a nicotine oxidizing enzyme. The inhibitory potencies of 26 naphthalene and 16 non-naphthalene derivatives were determined

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