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Troxipide

Catalog No. T6710   CAS 30751-05-4
Synonyms: Aplace

Troxipide (Aplace), a new-type systemic non-antisecretory gastric cytoprotective agent, which is mucus-secreting, anti-ulcer, and anti-inflammatory properties irrespective of pH of stomach or duodenum.

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Troxipide Chemical Structure
Troxipide, CAS 30751-05-4
Pack Size Availability Price/USD Quantity
100 mg In stock $ 50.00
1 mL * 10 mM (in DMSO) In stock $ 50.00
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Purity: 99.22%
Purity: 99.02%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description Troxipide (Aplace), a new-type systemic non-antisecretory gastric cytoprotective agent, which is mucus-secreting, anti-ulcer, and anti-inflammatory properties irrespective of pH of stomach or duodenum.
In vitro Troxipide is a new-type anti-ulcer compound that has an inhibitory effect on human neutrophil migration and has various agonist-induced activation. It inhibits neutrophil-mediated inflammation and oxidative stress but does not improve gastric mucus composition and output. In addition, it can increase the secretion of the prostaglandin, a cytoprotective agent.
In vivo Gastric mucosal metabolism and blood flow will be enhanced by Troxipide.
Kinase Assay Surface Plasmon Resonance (SPR) studies: The binding experiments are carried out on a ProteOn XPR36 biosensor at 25°C using the HTE sensor chip. The flow cells of the sensor chip are loaded with a nickel solution at 30 μL/min for 120 s to saturate the Tris–NTA surface with Ni(II) ions. Purified His-tagged STAT3 and STAT5 in PBST buffer (PBS with 0.005% (v/v) Tween-20 and 0.001% DMSO pH 7.4) is injected in the first and second channels of the chip respectively in the vertical direction at a flow rate of 25 μg/μL for 300 s, which attained, on average, ~8000 resonance unit (RU). After a wash with PBST buffer, inhibitors binding to the immobilized proteins is monitored by injecting a range of concentrations along with a blank at a flow rate of 100 μL/min for 200 s for each of these small molecules. When the injection of the small molecule inhibitor is completed, running buffer is allowed to flow over the immobilized substrates for the non-specifically bound inhibitors to dissociate for 600 s. Following dissociation of the inhibitors, the chip surface is regenerated with an injection of 1 M NaCl at a flow rate of 100 μL/ml for 18 s. Interspot channel reference is used for non-specific binding corrections and the blank channel used with each analyte injection served as a double reference to correct for possible baseline drift. Data are analyzed using ProteOn Manager Software version 3.1. The Langmuir 1:1 binding model was used to determine the KD values.
Synonyms Aplace
Molecular Weight 294.35
Formula C15H22N2O4
CAS No. 30751-05-4

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 15 mg/mL (51 mM)

Ethanol: 3 mg/mL (10.19 mM)

H2O: < 1 mg/mL (insoluble or slightly soluble)

TargetMolReferences and Literature

1. Kusugami K, et al. Dig Liver Dis, 2000, 32(4), 305-311. 2. Dewan B, et al. Gastroenterol Res Pract, 2010; 2010: 758397.

Related compound libraries

This product is contained In the following compound libraries:
Drug Repurposing Compound Library Orally Active Compound Library Bioactive Compounds Library Max FDA-Approved & Pharmacopeia Drug Library Anti-Aging Compound Library Ferroptosis Compound Library Approved Drug Library Anti-Fibrosis Compound Library Bioactive Compound Library NO PAINS Compound Library

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Keywords

Troxipide 30751-05-4 Others factor Inhibitor gastritis inhibit orally defensive ulcer antiulcer Aplace gastric inhibitor

 

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