S1413 |
Bafilomycin A1 (Baf-A1)
|
Bafilomycin A1(Baf-A1) is a vacuolar H+-ATPase inhibitor with IC50 of 0.44 nM. Bafilomycin A1 is found to inhibit autophagy while induces apoptosis. |
-
Nature, 2024, 626(8000):874-880
-
Nature, 2024, 626(8000):874-880
-
Cell, 2024, 187(21):6055-6070.e22
|
|
S1389 |
Omeprazole
|
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. |
-
J Extracell Vesicles, 2024, 13(4):e12426
-
J Extracell Vesicles, 2024, 13(4):e12426
-
J Transl Med, 2024, 22(1):676
|
|
S4845 |
Rabeprazole
|
Rabeprazole(LY307640) is an oral inhibitor of proton pump and blocks the production of acid by the stomach. |
-
J Extracell Vesicles, 2024, 13(4):e12426
-
Med Oncol, 2024, 41(8):188
-
PLoS Genet, 2022, 18(3):e1010128
|
|
S5658 |
Omeprazole Sodium
|
Omeprazole Sodium is the sodium salt form of omeprazole, which is a proton pump inhibitor and suppresses gastric acid secretion. Omeprazole Sodium is a metabolism-dependent inhibitor (MDI) of CYP2C19. |
-
Theranostics, 2021, 11(5):2364-2380
-
Theranostics, 2021, 11(5):2364-2380
-
J Virol, 2021, JVI.00190-21
|
|
S2105 |
Pantoprazole
|
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. |
-
Med Oncol, 2024, 41(8):188
-
Int J Mol Sci, 2022, 23-158572
-
Eur J Drug Metab Pharmacokinet, 2022, 10.1007/s13318-022-00780-x
|
|
S1354 |
Lansoprazole
|
Lansoprazole (A-65006, AG-1749) is a proton-pump inhibitor (PPI) that binds covalently to parietal cell H(+),K(+)-ATPase. Lansoprazole prevents the stomach from producing gastric acid. |
-
Front Cell Dev Biol, 2021, 9:655559
-
J Virol, 2021, JVI.00190-21
-
Front Microbiol, 2019, 10:2790
|
|
S4075 |
Zinc Pyrithione
|
Zinc pyrithione (OM-1563) is an antifungal and antibacterial agent disrupting membrane transport by blocking the proton pump. |
-
Cell Chem Biol, 2021, S2451-9456(21)00213-0
-
Biol Reprod, 2019, 100(2):468-478
-
Cell Syst, 2017, 4(6-:600-610
|
|
S4099 |
Dexlansoprazole
|
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. Dexlansoprazole selectively suppresses gastric acid secretion by direct inhibition of the H(+),K(+)-ATPase proton pump in the gastric parietal cell. |
-
J Virol, 2021, JVI.00190-21
-
Front Microbiol, 2019, 10:2790
|
|
S5608 |
Pantoprazole sodium hydrate
|
Pantoprazole (BY10232, SKF96022) sodium hydrate (Protonix) is a potent inhibitor of H+/K(+)-ATPase with IC50 of 6.8 μM. |
-
Eur J Drug Metab Pharmacokinet, 2022, 10.1007/s13318-022-00780-x
-
J Virol, 2021, JVI.00190-21
|
|
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. |
-
Eur J Drug Metab Pharmacokinet, 2022, 10.1007/s13318-022-00780-x
-
J Virol, 2021, JVI.00190-21
|
|
S5885 |
Rabeprazole Related Compound E
|
Rabeprazole Related Compound E (Rabeprazole thioether) is an active metabolite of rabeprazole, which is a proton pump inhibitor. |
-
Stem Cells Int, 2022, 2022:1396735
|
|
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. |
-
J Virol, 2021, JVI.00190-21
|
|
S3666 |
Ilaprazole
|
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. |
-
Med Oncol, 2024, 41(8):188
-
J Virol, 2021, JVI.00190-21
|
|
S4212 |
Tenatoprazole
|
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. Tenatoprazole labels only the gastric H(+),K(+)-ATPase alpha-subunit, approximately 2.6 nM/mg of tenatoprazole is bound to the H(+),K(+)-ATPase. |
-
J Virol, 2021, JVI.00190-21
|
|
S4665 |
Rabeprazole sodium
|
Rabeprazole (Aciphex, Dexrabeprazole, Habeprazole) is an antiulcer drug in the class of proton pump inhibitors. |
-
J Virol, 2021, JVI.00190-21
|
|
S5058 |
Revaprazan Hydrochloride
|
Revaprazan Hydrochloride (YH1885) is a new reversible proton pump inhibitor with long-lasting acid-suppressive effects. Revaprazan Hydrochloride reversibly inhibits H(+)/K(+)-ATPase via binding to the K+-binding site of the pump. |
-
ACS Infect Dis, 2021, 10.1021/acsinfecdis.0c00754
|
|
S1743 |
Esomeprazole magnesium
|
Esomeprazole Magnesium(NEXIUM) is a proton pump inhibitor to reduce gastric acid secretion through inhibition of H(+)/K(+)-ATPase in gastric parietal cells. |
|
|
S2222 |
PF-3716556
|
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. |
|
|
E4988New |
Vonoprazan Fumarate
|
Vonoprazan Fumarate(TAK-438), is a potent, orally active inhibitor of proton pump, specifically a potassium-competitive acid blocker (P-CAB), inhibiting H+,K+-ATPase activity in porcine gastric microsomes with an IC50 of 19 nM at pH 6.5. It exhibits potent antisecretory activity and can be used in research of acid-related disease. |
|
|
E4878New |
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. |
|
|
S5847 |
Ethacrynate Sodium
|
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. |
|
|
S6438 |
Ufiprazole
|
Ufiprazole (Omeprazole sulfide) is an intermediate used in the production of the gastric proton pump inhibitors omeprazole and esomeprazole. |
|
|
S1413 |
Bafilomycin A1 (Baf-A1)
|
Bafilomycin A1(Baf-A1) is a vacuolar H+-ATPase inhibitor with IC50 of 0.44 nM. Bafilomycin A1 is found to inhibit autophagy while induces apoptosis. |
- Nature, 2024, 626(8000):874-880
- Nature, 2024, 626(8000):874-880
- Cell, 2024, 187(21):6055-6070.e22
|
|
S1389 |
Omeprazole
|
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. |
- J Extracell Vesicles, 2024, 13(4):e12426
- J Extracell Vesicles, 2024, 13(4):e12426
- J Transl Med, 2024, 22(1):676
|
|
S4845 |
Rabeprazole
|
Rabeprazole(LY307640) is an oral inhibitor of proton pump and blocks the production of acid by the stomach. |
- J Extracell Vesicles, 2024, 13(4):e12426
- Med Oncol, 2024, 41(8):188
- PLoS Genet, 2022, 18(3):e1010128
|
|
S5658 |
Omeprazole Sodium
|
Omeprazole Sodium is the sodium salt form of omeprazole, which is a proton pump inhibitor and suppresses gastric acid secretion. Omeprazole Sodium is a metabolism-dependent inhibitor (MDI) of CYP2C19. |
- Theranostics, 2021, 11(5):2364-2380
- Theranostics, 2021, 11(5):2364-2380
- J Virol, 2021, JVI.00190-21
|
|
S2105 |
Pantoprazole
|
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. |
- Med Oncol, 2024, 41(8):188
- Int J Mol Sci, 2022, 23-158572
- Eur J Drug Metab Pharmacokinet, 2022, 10.1007/s13318-022-00780-x
|
|
S1354 |
Lansoprazole
|
Lansoprazole (A-65006, AG-1749) is a proton-pump inhibitor (PPI) that binds covalently to parietal cell H(+),K(+)-ATPase. Lansoprazole prevents the stomach from producing gastric acid. |
- Front Cell Dev Biol, 2021, 9:655559
- J Virol, 2021, JVI.00190-21
- Front Microbiol, 2019, 10:2790
|
|
S4075 |
Zinc Pyrithione
|
Zinc pyrithione (OM-1563) is an antifungal and antibacterial agent disrupting membrane transport by blocking the proton pump. |
- Cell Chem Biol, 2021, S2451-9456(21)00213-0
- Biol Reprod, 2019, 100(2):468-478
- Cell Syst, 2017, 4(6-:600-610
|
|
S4099 |
Dexlansoprazole
|
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. Dexlansoprazole selectively suppresses gastric acid secretion by direct inhibition of the H(+),K(+)-ATPase proton pump in the gastric parietal cell. |
- J Virol, 2021, JVI.00190-21
- Front Microbiol, 2019, 10:2790
|
|
S5608 |
Pantoprazole sodium hydrate
|
Pantoprazole (BY10232, SKF96022) sodium hydrate (Protonix) is a potent inhibitor of H+/K(+)-ATPase with IC50 of 6.8 μM. |
- Eur J Drug Metab Pharmacokinet, 2022, 10.1007/s13318-022-00780-x
- J Virol, 2021, JVI.00190-21
|
|
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. |
- Eur J Drug Metab Pharmacokinet, 2022, 10.1007/s13318-022-00780-x
- J Virol, 2021, JVI.00190-21
|
|
S5885 |
Rabeprazole Related Compound E
|
Rabeprazole Related Compound E (Rabeprazole thioether) is an active metabolite of rabeprazole, which is a proton pump inhibitor. |
- Stem Cells Int, 2022, 2022:1396735
|
|
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. |
- J Virol, 2021, JVI.00190-21
|
|
S3666 |
Ilaprazole
|
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. |
- Med Oncol, 2024, 41(8):188
- J Virol, 2021, JVI.00190-21
|
|
S4212 |
Tenatoprazole
|
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. Tenatoprazole labels only the gastric H(+),K(+)-ATPase alpha-subunit, approximately 2.6 nM/mg of tenatoprazole is bound to the H(+),K(+)-ATPase. |
- J Virol, 2021, JVI.00190-21
|
|
S4665 |
Rabeprazole sodium
|
Rabeprazole (Aciphex, Dexrabeprazole, Habeprazole) is an antiulcer drug in the class of proton pump inhibitors. |
- J Virol, 2021, JVI.00190-21
|
|
S5058 |
Revaprazan Hydrochloride
|
Revaprazan Hydrochloride (YH1885) is a new reversible proton pump inhibitor with long-lasting acid-suppressive effects. Revaprazan Hydrochloride reversibly inhibits H(+)/K(+)-ATPase via binding to the K+-binding site of the pump. |
- ACS Infect Dis, 2021, 10.1021/acsinfecdis.0c00754
|
|
S1743 |
Esomeprazole magnesium
|
Esomeprazole Magnesium(NEXIUM) is a proton pump inhibitor to reduce gastric acid secretion through inhibition of H(+)/K(+)-ATPase in gastric parietal cells. |
|
|
S2222 |
PF-3716556
|
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. |
|
|
E4988New |
Vonoprazan Fumarate
|
Vonoprazan Fumarate(TAK-438), is a potent, orally active inhibitor of proton pump, specifically a potassium-competitive acid blocker (P-CAB), inhibiting H+,K+-ATPase activity in porcine gastric microsomes with an IC50 of 19 nM at pH 6.5. It exhibits potent antisecretory activity and can be used in research of acid-related disease. |
|
|
E4878New |
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. |
|
|
S5847 |
Ethacrynate Sodium
|
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. |
|
|
S6438 |
Ufiprazole
|
Ufiprazole (Omeprazole sulfide) is an intermediate used in the production of the gastric proton pump inhibitors omeprazole and esomeprazole. |
|
|