85208
银离子载体 II
Selectophore™
别名:
6-氧杂-3,9-二硫杂二环[9.3.1]十五基-1(15),11-13-三烯, MAO
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关于此项目
经验公式（希尔记法）:
C12H16OS2
化学文摘社编号:
分子量:
240.38
PubChem Substance ID:
UNSPSC Code:
26111700
Beilstein/REAXYS Number:
4182633
MDL number:
product line
Selectophore™
mp
112-114 °C
SMILES string
C1CSCc2cccc(CSCCO1)c2
InChI
1S/C12H16OS2/c1-2-11-8-12(3-1)10-15-7-5-13-4-6-14-9-11/h1-3,8H,4-7,9-10H2
InChI key
FFJVWROXKBHBGI-UHFFFAOYSA-N
General description
请访问 传感器应用门户网站 了解更多信息。
Other Notes
用于固体 PVC 膜电极中的银离子载体
Legal Information
Selectophore is a trademark of Merck KGaA, Darmstadt, Germany
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Francisco de Asís Balaguer et al.
International journal of molecular sciences, 20(6) (2019-03-23)
It has been proposed that one of the mechanisms of taxane-site ligand-mediated tubulin activation is modulation of the structure of a switch element (the M-loop) from a disordered form in dimeric tubulin to a folded helical structure in microtubules. Here
Brittany A Matthews et al.
Drug and alcohol dependence, 185, 398-405 (2018-03-20)
A key component of alcohol dependence (AD), a severe form of alcohol use disorder, is the negative emotional state during withdrawal. Monoamine oxidase A (MAO-A) is an important enzyme that metabolizes monoamines and creates oxidative stress. Elevations in MAO-A level
Chang-Yang Li et al.
Bioactive materials, 5(1), 34-43 (2020-01-21)
Micro-arc oxidation (MAO) coating with outstanding adhesion strength to Mg alloys has attracted more and more attention. However, owing to the porous structure, aggressive ions easily invaded the MAO/substrate interface through the through pores, limiting long-term corrosion resistance. Therefore, a
J. Casabo et al.
J. Chem. Soc., Dalton Trans., 1969-1969 (1991)
Nikolay T Tzvetkov et al.
Journal of enzyme inhibition and medicinal chemistry, 32(1), 960-967 (2017-07-21)
Pharmacological and physicochemical studies of N-unsubstituted indazole-5-carboxamides (subclass I) and their structurally optimised N1-methylated analogues (subclass II), initially developed as drug and radioligand candidates for the treatment and diagnosis of Parkinson's disease (PD), are presented. The compounds are highly brain
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