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Proton Pump

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Proton Pump

Chemical Structure Cat. No. Product Name CAS No.
(R)-(+)-Pantoprazole magnesium salt Chemical Structure
BCP20280 (R)-(+)-Pantoprazole magnesium salt 657391-79-2
Pantoprazole is a proton pump inhibitor drug used for short-term treatment of erosion and ulceration of the esophagus caused by gastroesophageal reflux disease.
Concanamycin A Chemical Structure
BCP21840 Concanamycin A 80890-47-7
Concanamycin A is a specific inhibitor of V-type (vacuolar) H+-ATPase that displays > 2000-fold selectivity over other H+-ATPases (IC50 values are 9.2, > 20000, > 20000 and > 20000 nM for yeast V-type, F-type, P-type H+-ATPases and porcine P-type Na+,K+-ATPase respectively).
Ufiprazole Chemical Structure
BCP21782 Ufiprazole 73590-85-9
Omeprazole sulfide is a metabolite of Omeprazole, which is a proton pump inhibitor.
Bedakillin Chemical Structure
BCP21751 Bedakillin 654653-81-3
Bedakillin acts on the proton pump of the ATP-synthase enzyme , which is a different mechanism of action than for quinolones targeting DNA-gyrase .
Vonoprazan Fumarate Chemical Structure
BCP13238 Vonoprazan Fumarate 881681-01-2
Vonoprazan is a novel P-CAB (potassium-competitive acid blocker) that reversibly inhibits H+/K+, ATPase with IC50 of 19 nM (pH 6.5), controls gastric acid secretion.
Vonoprazan Chemical Structure
BCP13240 Vonoprazan 881681-00-1
Vonoprazan is a novel P-CAB (potassium-competitive acid blocker) that reversibly inhibits H+/K+ ATPase with IC50 of 19 nM (pH 6.5), controls gastric acid secretion.
Tenatoprazole Chemical Structure
BCP09130 Tenatoprazole 113712-98-4
Tenatoprazole, also known as TU-199, is a proton pump inhibitor drug candidate that was undergoing clinical testing as a potential treatment for reflux oesophagitis and peptic ulcer.
Lansoprazole N-Oxide Chemical Structure
BCP17470 Lansoprazole N-Oxide 213476-12-1
Lansoprazole N-Oxide (Lansoprazole EP Impurity A) is an impurity of Lansoprazole .
Chebulinic acid Chemical Structure
BCP09990 Chebulinic acid 18942-26-2
Chebulinic acid is a potent natural inhibitor of M. tuberculosis DNA gyrase, also can inhibit SMAD-3 phosphorylation, inhibit H+ K+-ATPase activity.
Rabeprazole Chemical Structure
BCP06638 Rabeprazole 117976-89-3
Rabeprazole is an antiulcer drug in the class of proton pump inhibitors.
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