| Cat. No. |
Product Name |
Information |
| PC-27263 |
Keverprazan
Potassium-competitive acid blocker
|
Keverprazan (H008, Carenoprazan) is a small molecule potassium-competitive acid blocker (P-CAB), shows potent and continuous gastric acid inhibition effect. |
| PC-27262 |
Keverprazan hydrochloride
Potassium-competitive acid blocker
|
Keverprazan hydrochloride (H008, Carenoprazan) is a small molecule potassium-competitive acid blocker (P-CAB), shows potent and continuous gastric acid inhibition effect. |
| PC-27037 |
Cladoniamide A
V-ATPase inhibitor
|
Cladoniamide A is a reversible broad-spectrum antiviral targets the human V-ATPase VO domain, interferes with V-ATPase-dependent acidification of the host endolysosomal network thus preventing viral entry. |
| PC-26887 |
NZ-58
Hv1 channel inhibitor
|
NZ-58 is a small molecule inhibitor of the HV1 voltage-gated proton channel with IC50 of 8.5 uM, also potently blocks voltage-gated Na+ and K+ channels at 50 uM, acts as a pan-VSD (voltage-sensor domains) modulator. |
| PC-26556 |
Dexlansoprazole
Proton Pump inhibitor
|
Dexlansoprazole ((R)-Lansoprazole) is the R enantiomer of Lansoprazole, which is a proton pump inhibitor, also binds to NTF2L domain of G3BP1 with Kd of 11 uM, reduces SARS-CoV-2 nucleocapsid protein (N) binds G3BP1 and inhibits viral replication. |
| PC-25409 |
Lansoprazole
Proton pump inhibitor
|
Lansoprazole (AG-1749) is an orally active proton pump inhibitor, inhibits db-cAMP-stimulated acid formation and (H+ + K+)-ATPase with IC50 of 59 nM and 2.1 uM respectively. |
| PC-24842 |
Pma1 inhibitor Si01
Pma1 inhibitor
|
Pma1 inhibitor Si01 is a specific inhibitor of P-type H+-ATPase (proton) Pma1 inhibitor, extends the chronological lifespan (CLS) in fission yeast. |
| PC-24753 |
Proton Pump inhibitor 1
Proton pump inhibitor
|
Proton Pump inhibitor 1 is a potent, selective proton pump inhibitor. |
| PC-24747 |
Ilaprazole sodium
Proton pump inhibitor
|
Ilaprazole sodium (IY-81149) is a potent, orally active proton pump inhibitor that irreversibly inhibits H+/K(+)-ATPase with IC50 of 6 uM. |
| PC-24746 |
Esomeprazole
Proton pump inhibitor
|
Esomeprazole is a proton pump inhibitor that reduces stomach acid secretion by inhibition of the H+/K+-ATPase in the parietal cells. |
| PC-24092 |
MFaN
Otop1 modulator
|
MFaN is a potent and specific positive allosteric modulator (PAM) of proton-gated proton channel Otop1, dose-dependently potentiates mOtop1 currents with EC50 of 10.3 uM (pH 5.5). |
| PC-23858 |
ClGBI
Hv1 channel inhibitor
|
ClGBI is a selective blocker/inhibitor of voltage-gated proton channel Hv1 (HVCN1) with Kd of 26 uM, induces acidification of leukemic Jurkat T cells promoting cell death by apoptosis. |
