| S1413 |
Bafilomycin A1 (Baf-A1)
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Bafilomycin A1 (Baf-A1) is a vacuolar H+-ATPase inhibitor with IC50 of 0.44 nM, and it is found to inhibit autophagy while inducing apoptosis.
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Cell & Bioscience, July 05, 2025, 96
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Journal of Cellular and Molecular Medicine, February 28, 2021, 3348-3360
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Cells, August 09, 2025, 1231
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| S1389 |
Omeprazole
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Omeprazole is a proton pump inhibitor that blocks H(+)-K(+)-ATPase, used to treat dyspepsia, peptic ulcer disease, gastroesophageal reflux disease, laryngopharyngeal reflux, and Zollinger–Ellison syndrome.
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Cells, 2025 Sep 24, 1489
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Gut, 2025, gutjnl-2024-334561
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Gut, 2025, nan
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| S4845 |
Rabeprazole
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Rabeprazole(LY307640) is an oral inhibitor of proton pump and blocks the production of acid by the stomach.
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J Extracell Vesicles, 2024, 13(4):e12426
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Sci Rep, 2024, 14(1):28163
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Med Oncol, 2024, 41(8):188
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| S1354 |
Lansoprazole
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Lansoprazole (A-65006, AG-1749) is a proton-pump inhibitor (PPI) that binds covalently to parietal cell H(+),K(+)-ATPase. This compound prevents the stomach from producing gastric acid.
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Journal of Virology, May 10, 2021, e00190-21
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bioRxiv, 2023, 548707
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Frontiers in Cell and Developmental Biology, 2021, 655559
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| S3666 |
Ilaprazole
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Ilaprazole (IY-81149) is a new proton pump inhibitor (PPI) used in the treatment of dyspepsia, peptic ulcer disease (PUD), gastroesophageal reflux disease (GORD/GERD) and duodenal ulcer. It inhibits H+/K+-ATPase with an IC50 of 6.0 μM.
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bioRxiv, May 19, 2025, 2025.05.19.654850
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Journal of Virology, May 10, 2021, 95(11):e00190-21
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Journal of Virology, June 10, 2021, 95(13):e02466-20
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| S2105 |
Pantoprazole
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Pantoprazole (SKF96022, BY-1023) is a proton pump inhibitor drug that inhibits gastric acid secretion. It works on gastric parietal cells to irreversibly inhibit (H+/K+)-ATPase function and suppress the production of gastric acid.
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Journal of Virology, May 10, 2021, e00190-21
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Med Oncol, 2024, 41(8):188
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Int J Mol Sci, 2022, 23-158572
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| S4665 |
Rabeprazole sodium
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Rabeprazole (Aciphex, Dexrabeprazole, Habeprazole) is an antiulcer drug in the class of proton pump inhibitors.
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Journal of Virology, 2021 May 10, e00190-21
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J Virol, 2021, JVI.00190-21
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Journal of Virology, 2021, e00190-21
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| S4099 |
Dexlansoprazole
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Dexlansoprazole (T 168390, TAK 390,(R)-Lansoprazole), the dextrorotatory enantiomer of lansoprazole, is a proton pump inhibitor (PPI) formulated to have dual delayed-release properties. This compound selectively suppresses gastric acid secretion by direct inhibition of the H(+),K(+)-ATPase proton pump in the gastric parietal cell.
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Food Chem Toxicol, 2025, 197:115262
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J Immunother Cancer, 2024, 12(11)e009805
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Journal of Virology, 2021, e00190-21
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| S5658 |
Omeprazole Sodium
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Omeprazole Sodium is the sodium salt form of omeprazole, which is a proton pump inhibitor and suppresses gastric acid secretion. This compound is a metabolism-dependent inhibitor (MDI) of CYP2C19.
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Theranostics, 2021, 11(5):2364-2380
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J Virol, 2021, JVI.00190-21
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Biosci Rep, 2021, BSR20200842
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| S4212 |
Tenatoprazole
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Tenatoprazole (TU-199,STU-Na) is a prodrug of the proton pump inhibitor (PPI) class, which inhibits proton transport with IC50 of 3.2 μM. This compound labels only the gastric H(+),K(+)-ATPase alpha-subunit, approximately 2.6 nM/mg of this chemical is bound to the H(+),K(+)-ATPase.
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Advanced Science, 2024, e2308312
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Viruses, 2024, 16(10)1566
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Journal of Virology, 2021, e02466-20
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| S4538 |
Pantoprazole sodium
|
Pantoprazole (SKF96022, BY-1023) is a proton pump inhibitor drug that inhibits gastric acid secretion. It works on gastric parietal cells to irreversibly inhibit (H+/K+)-ATPase function and suppress the production of gastric acid.
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Journal of Virology, May 10, 2021, e00190-21
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Eur J Drug Metab Pharmacokinet, 2022, 10.1007/s13318-022-00780-x
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J Virol, 2021, JVI.00190-21
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| S4075 |
Zinc Pyrithione
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Zinc pyrithione (OM-1563) is an antifungal and antibacterial agent disrupting membrane transport by blocking the proton pump.
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Cell Chem Biol, 2021, S2451-9456(21)00213-0
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Biol Reprod, 2019, 100(2):468-478
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Biology of Reproduction, 2019, 468–478
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| S1743 |
Esomeprazole magnesium
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Esomeprazole Magnesium(NEXIUM) is a proton pump inhibitor to reduce gastric acid secretion through inhibition of H(+)/K(+)-ATPase in gastric parietal cells.
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-
Scientific Reports, August 17, 2017, 8491
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Scientific Reports, 2017, 8491
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| S5885 |
Rabeprazole Related Compound E
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Rabeprazole Related Compound E (Rabeprazole thioether) is an active metabolite of rabeprazole, which is a proton pump inhibitor.
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-
Stem Cells Int, 2022, 2022:1396735
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| S5502 |
Ilaprazole sodium
|
Ilaprazole (IY-81149) sodium is the sodium salt form of ilaprazole, which is a proton pump inhibitor. Ilaprazole sodium irreversibly inhibits H(+)/K(+)-ATPase in a dose-dependent manner with IC50 of 6 μM in rabbit parietal cell preparation.
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-
J Virol, 2021, JVI.00190-21
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|
| E6009 |
Esomeprazole
|
Esomeprazole ((S)-Omeprazole, (-)-Omeprazole) is a potent inhibitor of proton pump. It decreases acid production by inhibiting the H+, K+-ATPase enzyme in gastric parietal cells. Esomeprazole displays pharmacokinetic properties that make it more effective than omeprazole and has the potential for use in research of symptomatic gastroesophageal reflux disease.
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Scientific Reports, August 17, 2017, 8491
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| S5058 |
Revaprazan Hydrochloride
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Revaprazan Hydrochloride (YH1885) is a new reversible proton pump inhibitor with long-lasting acid-suppressive effects. This compound reversibly inhibits H(+)/K(+)-ATPase via binding to the K+-binding site of the pump.
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-
ACS Infect Dis, 2021, 10.1021/acsinfecdis.0c00754
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| S2222 |
PF-3716556
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PF 3716556 is a potent and selective P-CAB (potassium-competitive acid blocker), with pIC50 of 6.026 and 7.095 for the inhibition of porcine H+,K+-ATPase activity in ion-leaky and ion-tight assay, respectively, inhibits gastric acid secretion, displays no activity at Na+,K+-ATPase, used for the treatment of gastroesophageal reflux disease.
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| E4878 |
Lansoprazole sodium
|
Lansoprazole Sodium, a sodium salt form of Lansoprazole, is an orally active inhibitor of proton pump, preventing the stomach from producing acid. Lansoprazole enhances the expression and transcriptional effectiveness of runt-related transcription factor 2 (Runx2), stimulating osteoprogenitor cell's commitment and differentiation toward their lineage.
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| S5847 |
Ethacrynate Sodium
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Ethacrynate Sodium (ethacrynic acid sodium) is the sodium salt form of ethacrynic acid, which inhibits symport of sodium, potassium, and chloride primarily in the ascending limb of Henle, but also in the proximal and distal tubules.
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| S6438 |
Ufiprazole
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Ufiprazole (Omeprazole sulfide) is an intermediate used in the production of the gastric proton pump inhibitors omeprazole and esomeprazole.
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|
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| S5608 |
Pantoprazole sodium hydrate
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Pantoprazole (BY10232, SKF96022) sodium hydrate (Protonix) is a potent inhibitor of H+/K(+)-ATPase with IC50 of 6.8 μM.
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-
Molecular Therapy, 2025, 336-355
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Eur J Drug Metab Pharmacokinet, 2022, 10.1007/s13318-022-00780-x
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Journal of Virology, 2021, e00190-21
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