Benzimidazoles
Sigma Aldrich Fine Chemicals Biosciences Omeprazole solid500MG
Omeprazole is a benzimidazole derivative a weak base and is lipophilic in nature. This compound is pH sensitive and does not exists in its original form at low pH.
Cayman Chemical Omeprazole sulfon-d3 1mg
An internal standard for the quantification of omeprazole sulfone by GC- or LC-MS
Medchemexpress LLC Omeprazole | 73590-58-6 | 100.0% | 1 G
Omeprazole (H 16868) is a proton pump inhibitor (PPI) used in the treatment of acid-related gastrointestinal disorders. It competitively inhibits CYP2C19 activity with a Ki of 2 to 6 μM. Omeprazole demonstrates inhibition of growth in both Gram-positive and Gram-negative bacteria and acts as a potent brain-penetrant neutral sphingomyelinase (N-SMase) inhibitor and exosome inhibitor.
- Proton pump inhibitor (PPI)
- Used for treating acid-related gastrointestinal disorders
- Competitively inhibits CYP2C19 activity (Ki of 2 to 6 μM)
- Inhibits growth of Gram-positive and Gram-negative bacteria
- Potent brain-penetrant neutral sphingomyelinase (N-SMase) inhibitor
- Acts as an exosome inhibitor
Medchemexpress LLC Omeprazole-d3 | 922731-01-9 | 99.0% | C17H16D3N3O3S | 1 MG
Omeprazole-d3 (H 16868-d3) is a deuterium-labeled version of Omeprazole. Omeprazole is a proton pump inhibitor (PPI) used in the treatment of acid-related gastrointestinal disorders, competitively inhibiting CYP2C19 activity and the growth of both Gram-positive and Gram-negative bacteria. The incorporation of stable heavy isotopes into drug molecules, such as deuterium, can influence the pharmacokinetic and metabolic profiles of drugs.
- Can be used as a tracer
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS
- Suitable for treatment of acid-related gastrointestinal disorders
- Inhibits growth of Gram-positive and Gram-negative bacteria
Apexbio Technology LLC Omeprazole 73590-58-6 100mg
Omeprazole (73590-58-6) is a small-molecule inhibitor targeting H K -ATPase an enzyme essential for gastric acid secretion It is designed to inhibit the proton pump thereby reducing active transport of H ions into the gastric lumen Omeprazole exerts its biological activity primarily through irreversible binding to the H K -ATPase enzyme In in vitro studies Omeprazole demonstrates inhibitory activity with an IC value of approximately 5 8 M against purified H K -ATPase and an IC of 0 16 M in assays evaluating histamine-induced gastric acid production Based on these pharmacological properties Omeprazole holds research potential in the investigation of acid-mediated gastrointestinal conditions and related pathways
Medchemexpress LLC Omeprazole sulfide-d3 (ufiprazole-d3) | 922730-98-1 | 99.8% | C17H16D3N3O2S | 1 MG
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
Medchemexpress LLC Omeprazole (standard) | 73590-58-6 | 99.86% | C17H19N3O3S | 25 MG
Omeprazole (Standard) is the analytical standard of Omeprazole, intended for research and analytical applications. It is a proton pump inhibitor (PPI) used to treat acid-related gastrointestinal disorders, 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 (exosome inhibitor).
- Used as a reference standard for assay
- Commonly used in qualitative, quantitative, and methodological research experiments
- Suitable for HPLC, GC, and MS applications
Apexbio Technology LLC Fenbendazole 43210-67-9 500mg
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
![Medchemexpress LLC 2-[(4-chloro-3,5-dimethylpyridin-2-yl)methylsulfanyl]-6-methoxy-1H-benzimidazole | 220757-74-4 | 50mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000267118.png-250.jpg)
Medchemexpress LLC 2-[(4-chloro-3,5-dimethylpyridin-2-yl)methylsulfanyl]-6-methoxy-1H-benzimidazole | 220757-74-4 | 50mg
Omeprazole impurity 13 is an impurity ofOmeprazole (HY-B0113)
Medchemexpress LLC Omeprazole | 73590-58-6 | 99.9% | 345.42 | 100 MG
Omeprazole is a proton pump inhibitor (PPI) used for treating acid-related gastrointestinal disorders. It competitively inhibits CYP2C19 activity and inhibits the growth of both Gram-positive and Gram-negative bacteria. Additionally, it is a potent brain penetrant neutral sphingomyelinase (N-SMase) inhibitor and an exosome inhibitor.
- Proton pump inhibitor (PPI)
- Competitively inhibits CYP2C19 activity
- Inhibits growth of Gram-positive and Gram-negative bacteria
- Potent brain penetrant neutral sphingomyelinase (N-SMase) inhibitor
- Exosome inhibitor
- Inhibits gastric acid secretion
- Acid-labile compound
Sigma Aldrich Fine Chemicals Biosciences Pantoprazole sodium hydrate >=98% (HPLC) | 718635-09-7 | 50MG
Pantoprazole sodium hydrate >=98% (HPLC) | Purity: >=98% (HPLC) | 718635-09-7 | 50MG
Cayman Chemical Omeprazole sulfIde 500mg
An active metabolite of omeprazole; has been used as a precursor in the synthesis of esomeprazole; a potential impurity in commercial preparations of omeprazole
Cayman Chemical 4-hydroxy Omeprazole sulfide
A metabolite of omeprazole; has been found in wastewater effluent
Medchemexpress LLC (R)-omeprazole sodium | 161796-77-6 | 98.1% | C17H18N3NaO3S | 10MG
(R)-omeprazole sodium is the R-enantiomer of omeprazole supplied as the sodium salt. It is a gastric acid-resistant proton pump inhibitor used as a research reference standard to study gastric acid secretion and CYP2C19-mediated metabolism. The compound is provided with high chemical and enantiomeric purity for analytical and pharmacology studies.
- Molecular formula: C17H18N3NaO3S.
- Molecular weight: 367.4 g/mol.
- Purity: 98.1% (reported 98.07%).
- Enantiomeric excess: 99.84%.
- Function: reversible and metabolism-dependent inhibitor of CYP2C19.
- Intended use: reference standard and research compound for pharmacology and metabolism studies.
- Availability: includes small-scale 10 mg quantities suitable for analytical work.