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Merck
CN

41593

Sigma-Aldrich

2-Ethoxy-2-(2-naphthyl)acetonitrile

≥95.0% (HPLC)

别名:

α-Ethoxy-2-naphthaleneacetonitrile

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关于此项目

经验公式(希尔记法):
C14H13NO
化学文摘社编号:
分子量:
211.26
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
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方案

≥95.0% (HPLC)

荧光

λex 227 nm; λem 336 nm in methanol

SMILES字符串

CCOC(C#N)c1ccc2ccccc2c1

InChI

1S/C14H13NO/c1-2-16-14(10-15)13-8-7-11-5-3-4-6-12(11)9-13/h3-9,14H,2H2,1H3

InChI key

SERAXWXRCADJHK-UHFFFAOYSA-N

应用

2-Ethoxy-2-(2-naphthyl)acetonitrile is a fluorogenic substrate for use in cytochrome P450 assays.

象形图

Environment

警示用语:

Warning

危险声明

预防措施声明

危险分类

Aquatic Acute 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves

法规信息

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分析证书(COA)

Lot/Batch Number

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Alexander Zawaira et al.
Pharmacogenetics and genomics, 18(6), 467-476 (2008-05-23)
We have used maximum-likelihood models of codon substitution to investigate the role of adaptive evolution in the evolution of cytochrome P450 (CYP) sequences. Evidence for the operation of adaptive evolution in the evolution of rat CYP2C, rabbit CYP2C, rat CYP2D
Alexander Zawaira et al.
Current drug metabolism, 12(7), 684-700 (2011-07-12)
The original map of mammalian cytochrome P450 (CYP450) residues involved in substrate recognition was prepared for the CYP2 family by Gotoh in 1992 by manual alignment of mammalian CYP450 residues with substrate recognition site (SRS) residues manually delimited from a
David S Wishart
Drugs in R&D, 8(6), 349-362 (2007-10-30)
Drug development is an intrinsically risky business. Like a high stakes poker game the entry costs are high and the probability of winning is low. Indeed, only a tiny percentage of lead compounds ever reach US FDA approval. At any

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