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Ebrotidine Inhibitor

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS5754814

Ebrotidine is a competitive H2-receptor antagonist (Ki: 127.5nM). It has a potent antisecretory activity and evidenced gastroprotection. More details

Product Documentation
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Sample Manual Insert View PDF
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Testing Data View PDF
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Certificate of Analysis (COA) View PDF
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QC Report View PDF
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Material Safety Data Sheet View PDF
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Technical Datasheet View PDF
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Protocol View PDF

Product Overview

Online Datasheet in PDF
Product Name
Ebrotidine, Inhibitor
Full Product Name
Ebrotidine
Product Synonym Names
FI3542
Form/Format
Solid. Powder
Purity/Purification
98.00%
Preparation and Storage
Store at -20 degree C for 3 years powder
-80 degree C for 2 years in solvent
Molecular Weight
477.42
Solubility
DMSO: 100mg/mL (209.46mM) Need ultrasonic
(<1mg/ml refers to the product slightly soluble or insoluble)
Formula
C14H17BrN6O2S3
SMILES
O=S(C1=CC=C(Br)C=C1)(/N=C/NCCSCC2=CSC(NC(N)=N)=N2)=O
CAS Number
100981-43-9
Target & IC50
Others
In Vitro
Ebrotidine inhibited histamine- and pentagastrin-stimulated acid secretion in a dose-dependent manner (ED50: 0.21 and 0.44mg/kg, respectively), following intravenous administration to rats [2]. Results of the macroscopic assessment revealed that ebrotidine at doses of 50mg and higher/kg body weight effectively prevented mucosal injury and that the maximal protective effect was achieved by 1hours. Physicochemical analysis established that ebrotidine evoked 30% increase in mucus gel dimension, and showed a 20% increase in phospholipids, and the content of sulfo- (18%) and sialomucins (21%) [4]. The mean number of gastric erosions seen at endoscopy after treatment with ebrotidine plus ASA (2.0 +/- 0.3) was obviously lower than that after placebo plus ASA (3.7 +/- 0.2). This reduction in lesion core by ebrotidine was accompanied by a significant increase in gastric blood flow (by 15% in corpus and 26% in antrum), by a rise in transmucosal potential difference (by 12%), and by a decrease of mucosal micro bleeding [3].

Product References and Citations for Ebrotidine, inhibitor

Agut J, Sanchez JC, Sacristan A, Action of ebrotidine, ranitidine and cimetidine on the specific binding to histamine H- and H2-receptors. Arzneimittelforschung. 1997 Apr;47(4A):447-9.
Agut J, Sanchez JC, Sacristan A, Action of ebrotidine, ranitidine and cimetidine on the specific binding to histamine H- and H2-receptors. Arzneimittelforschung. 1997 Apr;47(4A):447-9.
Palop D, Agut J, Marquez M, histamine H-receptor antagonist action of ebrotidine. Effects on gastric acid secretion, gastrin levels and NSAID-induced gastrotoxicity in the rat. Arzneimittelforschung. 1997 Apr;47(4A):439-46.
Palop D, Agut J, Marquez M, histamine H-receptor antagonist action of ebrotidine. Effects on gastric acid secretion, gastrin levels and NSAID-induced gastrotoxicity in the rat. Arzneimittelforschung. 1997 Apr;47(4A):439-46.
Konturek SJ, Kwiecien N, Sito E, Effects of ebrotidine on aspirin-induced gastric mucosal damage and blood flow in humans. Scand J Gastroenterol. 1993 Dec;28(12):1047-50.
Konturek SJ, Kwiecien N, Sito E, Effects of ebrotidine on aspirin-induced gastric mucosal damage and blood flow in humans. Scand J Gastroenterol. 1993 Dec;28(12):1047-50.
Piotrowski J, Yamaki K, Morita M, Ebrotidine--a new H2-receptor antagonist with mucosal strengthening activity. Biochem Int. 1992 Mar;26(4):659-67.
Piotrowski J, Yamaki K, Morita M, Ebrotidine--a new H2-receptor antagonist with mucosal strengthening activity. Biochem Int. 1992 Mar;26(4):659-67.

Other Notes

Small volumes of Ebrotidine, inhibitor vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

Searchable Terms for Ebrotidine purchase

MBS5754814 is an inhibitor targeting Ebrotidine.
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