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Merck
CN

I3377

Supelco

异烟肼

analytical standard, ≥99% (TLC)

别名:

4-吡啶羧酸酰肼, INH, 异烟酸肼, 雷米封

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关于此项目

经验公式(希尔记法):
C6H7N3O
CAS Number:
分子量:
137.14
Beilstein:
119374
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24
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等级

analytical standard

质量水平

方案

≥99% (TLC)

技术

HPLC: suitable
gas chromatography (GC): suitable

mp

171-173 °C (lit.)

荧光

λex 360 nm; λem 450 nm (thiol adduct)

抗生素抗菌谱

mycobacteria

应用

forensics and toxicology
pharmaceutical (small molecule)

包装形式

neat

SMILES字符串

NNC(=O)c1ccncc1

InChI

1S/C6H7N3O/c7-9-6(10)5-1-3-8-4-2-5/h1-4H,7H2,(H,9,10)

InChI key

QRXWMOHMRWLFEY-UHFFFAOYSA-N

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一般描述

化学结构式:吡啶
异烟肼是一类具有抗分枝杆菌活性的药物。用于结核病的治疗。

应用

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生化/生理作用

针对结核菌的抗生素,抑制分枝菌酸的生物合成。由肝脏 N-乙酰转移酶 (NAT) 和 细胞色素 P450 2E1 (CYP2E1) 代谢形成肝毒素。选择性诱导 CYP2E1 的表达。可逆抑制 CYP2C19 和 CYP3A4 的活性,在临床相关浓度下机械性地灭活 CYP1A2、CYP2A6、CYP2C19 和 CYP3A4。

其他说明

在我们的NMR在线平台ChemisTwin®上可以找到本品对应的数字化标准物质。您可使用ChemisTwin®上的数字等效品鉴定您的样品并进行定量分析(使用数字化外标)。还可查看该物质的NMR谱图。只需点击几次鼠标,就能进行在线样品比对。欢迎点击了解更多,开启免费试用之旅。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Skin Irrit. 2

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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We have designed and synthesized both the quinoline and naphthalene based molecules influenced by the unique structural make-up of mefloquine and TMC207, respectively. These compounds were evaluated for their anti-mycobacterial activity against drug sensitive Mycobacterium tuberculosis H37Rv in vitro at
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Bioorganic & medicinal chemistry, 17(7), 2830-2841 (2009-03-17)
We herein describe the synthesis and antimycobacterial activity of a series of 27 different derivatives of 3-benzyl-6-bromo-2-methoxy-quinolines and amides of 2-[(6-bromo-2-methoxy-quinolin-3-yl)-phenyl-methyl]-malonic acid monomethyl ester. The antimycobacterial activity of these compounds was evaluated in vitro against Mycobacterium tuberculosis H37Rv for nine
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Han DC, et al.
Clinical Orthopaedics and Related Research, 471(7), 2400-2406 (2013)
Kamaljit Singh et al.
European journal of medicinal chemistry, 46(6), 2290-2294 (2011-04-01)
A series of pyrimidine derivatives bearing amine substituents at C-2 position were obtained from Biginelli 3,4-dihydropyrimidin-2(1H)-ones and the effect of structural variation on anti-TB activity against Mycobacterium tuberculosis H37Rv strain and antiviral activity in a series of cell cultures was
Chang Dong Han et al.
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