Cariporide
Chemical Name: N-(Aminoiminomethyl)-4-(1-methylethyl)-3-(methylsulfonyl)benzamide
Purity: ≥98%
Biological Activity
Cariporide is a selective Na+/H+ exchanger isoform 1 (NHE1) inhibitor (IC50 values are 0.05, 3 and 1000 μM for NHE1, NHE3 and NHE2 respectively). Attenuates ischemia-induced cardiomyocyte apoptosis in vitro. Reduces cardiac arrhythmia in vivo. Also promotes apoptosis in cancer cells overexpressing NHE1. Orally active.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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Protective effects of HOE642, a selective sodium-hydrogen exchange subtype 1 inhibitor, on cardiac ischaemia and reperfusion.
Scholz et al.
Cardiovasc.Res., 1995;29:260 -
A rapid ischemia-induced apoptosis in isolated rat hearts and its attenuation by the sodium-hydrogen exchange inhibitor HOE 642 (cariporide).
Chakrabarti et al.
J.Mol.Cell.Cardiol., 1997;29:3169 -
Cariporide (HOE642), a selective Na+-H+ exchange inhibitor, inhibits the mitochondrial death pathway.
Teshima et al.
Circulation, 2003;108:2275 -
Cariporide and other new and powerful NHE1 inhibitors as potentially selective anticancer drugs--an integral molecular/biochemical/metabolic/clinical approach after one hundred years of cancer research.
Harguindey et al.
J.Transl.Med., 2013;11:282
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Citation for Cariporide
The citations listed below are publications that use Tocris products. Selected citations for Cariporide include:
1 Citation: Showing 1 - 1
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Solute exchange through gap junctions lessens the adverse effects of inactivating mutations in metabolite-handling genes.
Authors: Alzbeta Et al.
Elife 2022;11
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