P2880
Propionylthiocholine iodide
≥98%
Synonym(s):
(2-Mercaptoethyl)trimethylammonium iodide propionate
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5 G
$172.00
25 G
$734.00
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5 G
$172.00
25 G
$734.00
About This Item
Linear Formula:
C8H18NOSI
CAS Number:
Molecular Weight:
303.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
≥98%
form
powder
mp
200-202 °C (lit.)
storage temp.
−20°C
SMILES string
[I-].CCC(=O)SCC[N+](C)(C)C
InChI
1S/C8H18NOS.HI/c1-5-8(10)11-7-6-9(2,3)4;/h5-7H2,1-4H3;1H/q+1;/p-1
InChI key
BJQIXLJDWWVGAE-UHFFFAOYSA-M
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Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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J M Monserrat et al.
Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology, 120(2), 193-199 (1998-11-25)
In this study, some kinetic and toxicological parameters of the thoracic ganglia cholinesterase from the estuarine crab Chasmagnathus granulata were determined. Effects of the type and concentration of substrate, pH (6.80-8.50), incubation temperature (5-35 degrees C) and eserine on the
Patricia G Rodrigues et al.
American journal of physiology. Heart and circulatory physiology, 316(3), H459-H475 (2018-12-12)
Several studies have demonstrated that administration of doxorubicin (DOXO) results in cardiotoxicity, which eventually progresses to dilated cardiomyopathy. The present work aimed to evaluate the early myocardial changes of DOXO-induced cardiotoxicity. Male New Zealand White rabbits were injected intravenously with
R N Guedes et al.
Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology, 119(2), 205-210 (1998-07-21)
Acetylcholinesterase (AChE, EC 3.1.1.7) purified from the lesser grain borer (Rhyzopertha dominica) was significantly inhibited by higher concentrations of the substrates acetylthiocholine (ATC), acetyl-(beta-methyl) thiocholine (A beta MTC) and propionylthiocholine (PTC). 2. The efficiency of AChE for hydrolyzing different substrates
J Trancard et al.
Brain research, 476(2), 213-219 (1989-01-09)
The cholinesterase equipment of cerebral microvessels was studied in some rodents and carnivores using the Koelle-Friedenwald histochemical method with 3 artificial substrates and specific inhibitors for butyrylcholinesterase or acetylcholinesterase. Our observations reveal a great heterogeneity in cholinesterase types and their
Andreea Ticu Boeck et al.
Biochemical pharmacology, 63(12), 2101-2110 (2002-07-12)
The rat is the model animal for toxicity studies. Butyrylcholinesterase (BChE), being sensitive to inhibition by some organophosphorus and carbamate pesticides, is a biomarker of toxic exposure. The goal of this work was to characterize the purified rat BChE enzyme.
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