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Omeprazole sulfide-d3 is the deuterium labeled Omeprazole sulfide. Omeprazole metabolite Omeprazole sulfide (Ufiprazole) is a metabolite of Omeprazole, which is a proton pump inhibitor. It can be used as a tracer and as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS. This product is for research use only.
Deuterium labeled
Metabolite of Omeprazole
Proton pump inhibitor
Suitable as a tracer
Suitable as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
For research use only
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Omeprazole (Standard) is an analytical reference standard of omeprazole supplied as a purified solid for research and analytical applications. It is intended for use in assay calibration, method development, and quality control, and is documented with a certificate of analysis.
High reported purity (99.9%).
Chemical formula C17H19N3O3S and molecular weight 345.42 g/mol.
Provided as a 10 MG pack for analytical use.
Suitable for assay calibration and method development.
Characterized by a downloadable datasheet and COA.
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Omeprazole sulfide-d3 is the deuterium labeled form of Omeprazole sulfide, a metabolite of the proton pump inhibitor Omeprazole. It serves as a tracer and internal standard for quantitative analysis by NMR, GC-MS, or LC-MS. Deuteration can impact drug pharmacokinetic and metabolic profiles.
Deuterium labeled omeprazole sulfide
Metabolite of omeprazole, a proton pump inhibitor
Used as a tracer
Functions as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
For research use only
Prepare working solutions fresh for in vivo experiments
Heat or sonicate for dissolution if precipitation occurs
Store powder at -20°C for 3 years or 4°C for 2 years
Store in solvent at -80°C for 6 months or -20°C for 1 month
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Albendazole Oxide (Ricobendazole Albendazole sulfoxide) is a tubulin polymerization or assembly inhibitor used for the treatment of a variety of parasitic worm infestations
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Omeprazole is a proton pump inhibitor (PPI) used for treating acid-related gastrointestinal disorders. It competitively inhibits CYP2C19 activity and inhibits the growth of Gram-positive and Gram-negative bacteria. Additionally, it is a potent brain-penetrant neutral sphingomyelinase (N-SMase) inhibitor, functioning as an exosome inhibitor.
Proton pump inhibitor (PPI)
Used for treating acid-related gastrointestinal disorders
Competitively inhibits CYP2C19 activity
Inhibits the growth of Gram-positive and Gram-negative bacteria
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Omeprazole-d3 is a deuterium labeled form of Omeprazole, a proton pump inhibitor (PPI) used for acid-related gastrointestinal disorders. It competitively inhibits CYP2C19 activity (Ki of 2 to 6 μM) and also inhibits the growth of Gram-positive and Gram-negative bacteria. This compound can be used as a tracer and an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
Deuterium labeled compound
Acts as a proton pump inhibitor
Inhibits CYP2C19 activity
Inhibits growth of Gram-positive and Gram-negative bacteria
Suitable as a tracer for quantitative analysis
Functions as an internal standard for quantitative analysis
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Albendazole (CAS 54965-21-8) is a small-molecule inhibitor targeting tubulin It is designed to disrupt microtubule assembly thereby impairing cellular cytoskeletal function and parasite viability Albendazole exerts its biological activity primarily through binding to tubulin and inhibiting microtubule polymerization In tumor cell-based assays Albendazole demonstrates antiproliferative activity and induces cell cycle arrest autophagy and apoptosis with reported IC50 values typically ranging from 0 1 to 1 M depending on cell line and experimental conditions Based on these pharmacological properties Albendazole holds research potential in studies of parasitic infections microtubule dynamics tumor cell proliferation angiogenesis and programmed cell death
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Fenbendazole (CAS 43210-67-9) is a small-molecule inhibitor targeting microtubule polymerization It is designed to bind tubulin and disrupt microtubule dynamics thereby impairing cytoskeletal integrity and protein homeostasis Fenbendazole exerts its biological activity primarily through microtubule destabilization and disruption of proteasomal function triggering the unfolded protein response (UPR) pathway In various cancer cell lines fenbendazole demonstrates cytotoxic and anti-proliferative activity with reported IC50 values generally ranging from approximately 0 5 to 5 M Based on these pharmacological properties fenbendazole holds research potential in antiparasitic therapy and cancer drug repurposing studies
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An active metabolite of omeprazole; has been used as a precursor in the synthesis of esomeprazole; a potential impurity in commercial preparations of omeprazole
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