138786-67-1
Chemical Structure
Pantoprazole sodium
Synonym(s): BY1023 sodium; SKF96022 sodium
- CAS No.: 138786-67-1
- Formula:C16H14F2N3NaO4S
- Molecular Weight:405.35
IUPAC Name: sodium 6-(difluoromethoxy)-2-(((3,4-dimethoxypyridin-2-yl)methyl)sulfinyl)benzo[d]imidazol-1-ide
InChIKey: YNWDKZIIWCEDEE-UHFFFAOYSA-N
SMILES: O=S(C1=NC2=CC=C(OC(F)F)C=C2[N-]1)CC3=NC=CC(OC)=C3OC.[Na+]
Biological Activity: Pantoprazole sodium (BY10232 sodium) is an orally active and potent proton pump inhibitor (PPI)[1]. Pantoprazole sodium, a substituted benzimidazole, is a potent H+/K+-ATPase inhibitor with an IC50 of 6.8 μM. Pantoprazole sodium improves pH stability and has anti-secretory, anti-ulcer activities. Pantoprazole sodium significantly increased tumor growth delay combined with Doxorubicin (HY-15142)[3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
Pantoprazole sodium | 99.84% | Pantoprazole sodium (BY10232 sodium) is an orally active and potent proton pump inhibitor (PPI). Pantoprazole sodium, a substituted benzimidazole, is a potent H+/K+-ATPase inhibitor with an IC50 of 6.8 μM. Pantoprazole sodium improves pH stability and has anti-secretory, anti-ulcer activities. Pantoprazole sodium significantly increased tumor growth delay combined with Doxorubicin (HY-15142). | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Pantoprazole sodium (Standard) | ≥98% | Pantoprazole (sodium) (Standard) is the analytical standard of Pantoprazole (sodium). This product is intended for research and analytical applications. Pantoprazole sodium (BY10232 sodium) is an orally active and potent proton pump inhibitor (PPI). Pantoprazole sodium, a substituted benzimidazole, is a potent H+/K+-ATPase inhibitor with an IC50 of 6.8 μM. Pantoprazole sodium improves pH stability and has anti-secretory, anti-ulcer activities. Pantoprazole sodium significantly increased tumor growth delay combined with Doxorubicin (HY-15142). | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Pantoprazole-d8 sodium | Pantoprazole-d8 (BY1023-d8) sodium is a deuterium labeled Pantoprazole (HY-17507). Pantoprazole (BY10232) is an orally active and potent proton pump inhibitor (PPI). Pantoprazole, a substituted benzimidazole, is a potent H+/K+-ATPase inhibitor with an IC50 of 6.8 μM. Pantoprazole improves pH stability and has anti-secretory, anti-ulcer activities. Pantoprazole significantly increased tumor growth delay combined with Doxorubicin (HY-15142). | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
-
Similarity Score 0.83
HY-17507Pantoprazole -
Similarity Score 0.77
HY-Z3707N3-Methyl pantoprazole -
Similarity Score 0.77
HY-W703279(R)-(+)-Pantoprazole sodium -
Similarity Score 0.76
HY-Z2008Pantoprazole impurity 5 -
Similarity Score 0.75
HY-17507ES-Pantoprazole sodium trihydrate -
Similarity Score 0.75
HY-117225Pantoprazole sulfone -
Similarity Score 0.74
HY-17507S1Pantoprazole-d3 -
Similarity Score 0.73
HY-W016033Pantoprazole sulfide -
Similarity Score 0.70
HY-132485SN-Methyl Pantoprazole-d3 (Mixture of 1 and 3 isomers) -
Explore the MedChemAI to find more analogs
References
- [1]. Krupa J Patel, et al. Use of the proton pump inhibitor pantoprazole to modify the distribution and activity of doxorubicin: a potential strategy to improve the therapy of solid tumors. Clin Cancer Res. 2013 Dec 15;19(24):6766-76. [Content Brief]
- [3]. W Beil, et al. Pantoprazole: a novel H+/K(+)-ATPase inhibitor with an improved pH stability. Eur J Pharmacol. 1992 Aug 6;218(2-3):265-71. [Content Brief]
- [4]. K Takeuchi, et al. Effects of pantoprazole, a novel H+/K+-ATPase inhibitor, on duodenal ulcerogenic and healing responses in rats: a comparative study with omeprazole and lansoprazole. J Gastroenterol Hepatol. 1999 Mar;14(3):251-7. [Content Brief]
