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Merck
CN

264938

1-甲基异喹啉

97%

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关于此项目

经验公式(希尔记法):
C10H9N
化学文摘社编号:
分子量:
143.19
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
217-017-6
MDL number:
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产品名称

1-甲基异喹啉, 97%

InChI key

PBYMYAJONQZORL-UHFFFAOYSA-N

InChI

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

SMILES string

Cc1nccc2ccccc12

assay

97%

form

liquid

refractive index

n20/D 1.6140 (lit.)

bp

126-128 °C/16 mmHg (lit.)

density

1.078 g/mL at 25 °C (lit.)

Gene Information

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

Disclaimer

低熔点固体

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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历史批次信息供参考:

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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