跳转至内容
Merck

B3253

Sigma-Aldrich

碘化丁酰硫代胆碱

≥98%

别名:

(2-巯乙基)三甲基碘化铵丁酸酯

登录查看公司和协议定价


About This Item

线性分子式:
(CH3)3N(I)CH2CH2SCOCH2CH2CH3
CAS号:
分子量:
317.23
Beilstein:
3729509
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

≥98%

形狀

powder

mp

171-174 °C (lit.)

儲存溫度

−20°C

SMILES 字串

[I-].CCCC(=O)SCC[N+](C)(C)C

InChI

1S/C9H20NOS.HI/c1-5-6-9(11)12-8-7-10(2,3)4;/h5-8H2,1-4H3;1H/q+1;/p-1

InChI 密鑰

WEQAAFZDJROSBF-UHFFFAOYSA-M

正在寻找类似产品? 访问 产品对比指南

一般說明

碘化丁酰硫胆碱是丁酰胆碱的一种含硫类似物,用作丁酰胆碱酯酶活性测定试剂。

應用

  • 丁酰胆碱酯酶的无标记、超灵敏检测:研究采用基于Mn(II)的电子自旋共振波谱法,超灵敏检测丁酰胆碱酯酶。在有机磷农药存在下,以碘化丁酰硫代胆碱为底物测定酶活性。代表生化试验应用。(Tang et al., 2022)。
  • 用于生物传感的新型纳米酶:研发开发了一种Co, N共掺的多孔碳基纳米酶,可作为类氧化酶用于丁酰胆碱酯酶的荧光和比色法生物传感检测。其中,碘化丁酰硫代胆碱为关键底物。代表酶动力学分析相关应用(Sun et al., 2022)。
  • 抗阿兹海默症′药物筛选的检测系统:研究构建了铜纳米簇和MnO2纳米片荧光检测平台,用于检测丁酰胆碱酯酶活性(利用碘化丁酰硫代胆碱),继而可用于筛选抗阿兹海默病′药物,并检测胆碱能系统相互作用(Chen et al., 2022)。
  • 丁酰胆碱酯酶的双通道检测:研究介绍了融合荧光和氧化酶活性的双功能金属有机框架,开发用于双通道检测丁酰胆碱酯酶(使用碘化丁酰硫代胆碱),改进生化试验方法。(Wang et al., 2022)。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Ganiyu Oboh et al.
Neurotoxicology, 77, 12-19 (2019-12-15)
Many plant foods are rich sources of rutin, a flavonoid with many biological activities and health benefits. Exposure to cadmium has been implicated in neurotoxicity and cognitive dysfunction in animal models. However, there is a dearth of information on the
Cristobal Narvaez et al.
Chemosphere, 135, 75-82 (2015-04-29)
Inhibition of blood esterase activities by organophosphate (OP) pesticides has been used as a sensitive biomarker in birds. Furthermore, compared to mammalian vertebrates, less is known about the role of these enzyme activities in the digestive tracts of non-mammalian vertebrates
Gabriela Fernandes et al.
The journal of adhesive dentistry, 22(3), 265-274 (2020-05-22)
To investigate whether dental adhesives modified with polyacrylic acid copper iodide particles could inhibit esterase activity in vitro and the copper release rate from resin matrices, as well as the correlation between the two variables. Different concentrations of copper iodide
Oya Unsal-Tan et al.
MedChemComm, 10(6), 1018-1026 (2019-07-16)
A novel series of 2-pyrazoline derivatives were designed, synthesized, and evaluated for cholinesterase (ChE) inhibitory, Aβ anti-aggregating and neuroprotective activities. Among these, 3d, 3e, 3g, and 3h were established as the most potent and selective BChE inhibitors (IC50 = 0.5-3.9
Gabriele Horn et al.
Archives of toxicology, 89(3), 405-414 (2014-06-11)
Organophosphorus compounds (OP) are bound to human butyrylcholinesterase (BChE) and endogenous or exogenous BChE may act as a stoichiometric scavenger. Adequate amounts of BChE are required to minimize toxic OP effects. Simultaneous administration of BChE and oximes may transfer the

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系技术服务部门