922731-04-2

Esomeprazole-d<sub>6</sub> sodium Chemical Structure
922731-04-2

Chemical Structure

Esomeprazole-d6 sodium

Synonym(s): (S)-Omeprazole-d6 sodium; (-)-Omeprazole-d6 sodium

  • CAS No.: 922731-04-2
  • Formula:C17H13D6N3NaO3S
  • Molecular Weight:374.44

IUPAC Name: 3-ethynyl-4-methoxybenzoic acid

InChIKey: HVAJOLFRLWQQQL-ZGKVGPQDSA-N

SMILES: CC(C(OC([2H])([2H])[2H])=C(C=N1)C)=C1C[S@@](C(NC2=C3)=NC2=CC=C3OC([2H])([2H])[2H])=O.[Na]

Biological Activity: Esomeprazole-d6 sodium is the deuterium labeled Esomeprazole. Esomeprazole ((S)-Omeprazole) is a potent and orally active proton pump inhibitor and reduces acid secretion through inhibition of the H+, K+-ATPase in gastric parietal cells. Esomeprazole has the potential for symptomatic gastroesophageal reflux disease research[1][2][3].

Cat. No. Product Name Purity Description Pricing
HY-17023S
Esomeprazole-d6 sodium Esomeprazole-d6 sodium is the deuterium labeled Esomeprazole. Esomeprazole ((S)-Omeprazole) is a potent and orally active proton pump inhibitor and reduces acid secretion through inhibition of the H+, K+-ATPase in gastric parietal cells. Esomeprazole has the potential for symptomatic gastroesophageal reflux disease research.
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HY-17023R
Esomeprazole sodium (Standard) ≥98% Esomeprazole (sodium) (Standard) is the analytical standard of Esomeprazole (sodium). This product is intended for research and analytical applications. Esomeprazole sodium ((S)-Omeprazole sodium) is a potent and orally active proton pump inhibitor. Esomeprazole reduces acid secretion through inhibition of the H+, K+-ATPase in gastric parietal cells. Esomeprazole acts as an exosome inhibitor by blocking the exosome release via the inhibition of V-H+-ATPases. Esomeprazole has the potential for symptomatic gastroesophageal reflux disease research.
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HY-17023
Esomeprazole sodium 99.88% Esomeprazole sodium ((S)-Omeprazole sodium) is a potent and orally active proton pump inhibitor. Esomeprazole reduces acid secretion through inhibition of the H+, K+-ATPase in gastric parietal cells. Esomeprazole acts as an exosome inhibitor by blocking the exosome release via the inhibition of V-H+-ATPases. Esomeprazole has the potential for symptomatic gastroesophageal reflux disease research.
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