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Merck
CN

329061

Sigma-Aldrich

2-巯基吡啶-N-氧化物 钠盐

95%

别名:

1-Oxo-2-pyridinethiol sodium salt, 2-Pyridinethiol N-oxide sodium salt, Sodium (2-pyridylthio-1-oxide), Sodium 2-mercaptopyridine 1-oxide, Sodium 2-mercaptopyridine N-oxide

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About This Item

经验公式(希尔记法):
C5H4NNaOS
CAS号:
分子量:
149.15
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

95%

溶解性

water: soluble 0.5 g/10 mL, clear, colorless to light yellow

SMILES字符串

O.[O-][n+]1ccccc1S[Na]

InChI

1S/C5H5NOS.Na/c7-6-4-2-1-3-5(6)8;/h1-4,8H;/q;+1/p-1

InChI key

WNGMMIYXPIAYOB-UHFFFAOYSA-M

一般描述

2-Mercaptopyridine N-oxide acts as labelling agent during indium-111 labelling of human platelets. It acts as bioactive ligand and forms palladium and platinum complexes, which were tested as potential antitrypanosomal agents.

应用

2-巯基吡啶-N-氧化物的化学作用,请参见 Aldrichimica Acta

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 1

靶器官

Nervous system

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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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Y Isaka et al.
European journal of nuclear medicine, 18(5), 326-331 (1991-01-01)
Human platelets were labelled in the absence or presence of plasma using indium-111 labelled oxine sulphate, tropolone or 2-mercaptopyridine-N-oxide (MPO). Under in vitro and in vivo conditions, platelet functions were evaluated by measuring their aggregability, survival, recovery and early distribution.
Marisol Vieites et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 13(5), 723-735 (2008-03-07)
In the search for new therapeutic tools against Chagas disease (American trypanosomiasis) palladium and platinum complexes of the bioactive ligand pyridine-2-thiol N-oxide were exhaustively characterized and evaluated in vitro. Both complexes showed high in vitro growth inhibition activity (IC(50) values
Aldrichimica Acta, 20, 35-35 (1987)

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