46 Results for "

Na+/H+ exchanger

" in MedChemExpress (MCE) Product Catalog:
Products (46)

46 Results for "Na+/H+ exchanger" in MCE Product Catalog:

112
112 Publications Verification
Cat. No.: HY-101840
CAS No.: 1154-25-2
Purity:  99.73%
Synonyms: L593754; MH 12-43; Ethylisopropylamiloride
EIPA (L593754) is an orally active TRPP3 channel inhibitor with an IC50 of 10.5 μM. EIPA also enhances autophagy by inhibiting Na +/H +-exchanger 3 (NHE3). EIPA inhibits macropinocytosis as well. EIPA can be used in the research of inflammation and cancers, such as gastric cancer, colon carcinoma, pancreatic carcinoma .
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112
112 Publications Verification
Cat. No.: HY-101840A
CAS No.: 1345839-28-2
Purity:  98.31%
Synonyms: L593754 hydrochloride; MH 12-43 hydrochloride; Ethylisopropylamiloride hydrochloride
EIPA (L593754) hydrochloride is an orally active TRPP3 channel inhibitor with an IC50 of 10.5 μM. EIPA hydrochloride also enhances autophagy by inhibiting Na +/H +-exchanger 3 (NHE3). EIPA hydrochloride inhibits macropinocytosis as well. EIPA hydrochloride can be used in the research of inflammation and cancers, such as gastric cancer, colon carcinoma, pancreatic carcinoma .
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44
44 Cited Publications
Cat. No.: HY-N0150
CAS No.: 22373-78-0
Synonyms: Monensin A sodium
Monensin (Monensin A) sodium, an orally active antibiotic, is an ionophore that mediates Na +/H + exchange. Monensin sodium is a potent Wnt signaling inhibitor. Monensin sodium causes a marked enlargement of the multivesicular bodies (MVBs) and regulates exosome secretion. Monensin sodium can be used for bacterial, fungal, and parasitic infections research, and shows anticancer effects .
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44
44 Cited Publications
Cat. No.: HY-N4302
CAS No.: 17090-79-8
Synonyms: Monensin A
Monensin (Monensin A), an orally active antibiotic, is an ionophore that mediates Na +/H + exchange. Monensin is a potent Wnt signaling inhibitor. Monensin causes a marked enlargement of the multivesicular bodies (MVBs) and regulates exosome secretion. Monensin can be used for bacterial, fungal, and parasitic infections research, and shows anticancer effects .
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12
12 Cited Publications
Cat. No.: HY-19693
CAS No.: 159138-80-4
Synonyms: HOE-642 Free Base
Cariporide (HOE-642) is a selective Na +/H + exchange inhibitor.
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4
4 Cited Publications
Cat. No.: HY-19273
CAS No.: 187870-78-6
Synonyms: EMD-87580
Research Areas:  

Metabolic Disease

Rimeporide (EMD-87580) is a potent and selective inhibitor of the Na +/H + exchanger (NHE-1).
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3
3 Cited Publications
Cat. No.: HY-128067
CAS No.: 1428-95-1
Purity:  99.14%
Synonyms: Hexamethylene amiloride; HMA
Research Areas:  

Infection Cancer

5-(N,N-Hexamethylene)-amiloride (Hexamethylene amiloride) derives from an amiloride and is a potent Na +/H + exchanger inhibitor, which decreases the intracellular pH (pHi) and induces apoptosis in leukemic cells. 5-(N,N-Hexamethylene)-amiloride (Hexamethylene amiloride) is also an inhibitor of the HIV-1 Vpu virus ion channel and inhibits mouse hepatitis virus (MHV) replication and human coronavirus 229E (HCoV229E) replication in cultured L929 cells with EC50s of 3.91 μM and 1.34 μM, respectively .
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2
2 Cited Publications
Cat. No.: HY-105064D
CAS No.: 863406-85-3
Purity:  99.37%
Synonyms: CP-597396 hydrochloride hydrate
Zoniporide hydrochloride hydrate (CP-597396 hydrochloride hydrate) is a selective Na +/H + exchanger subtype 1 (NHE1) inhibitor with cardioprotective activity, with IC50 values of 67 nM and 73 nM against rat NHE1. Zoniporide hydrochloride hydrate reduces intracellular Na + and Ca 2+ overload, preserves mitochondrial integrity, activates pro-survival ERK1/2 and STAT3 signaling pathways, reduces necrosis and apoptosis, and decreases neutrophil aggregation. Zoniporide hydrochloride hydrate is applicable to research related to myocardial ischemia-reperfusion injury and heart graft ischemia-reperfusion injury .
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2
2 Cited Publications
Cat. No.: HY-105064
CAS No.: 241800-98-6
Purity:  99.89%
Synonyms: CP-597396
Zoniporide (CP-597396) is a selective Na +/H + exchanger subtype 1 (NHE1) inhibitor with cardioprotective activity, with IC50 values of 67 nM and 73 nM against rat NHE1. Zoniporide reduces intracellular Na + and Ca 2+ overload, preserves mitochondrial integrity, activates pro-survival ERK1/2 and STAT3 signaling pathways, reduces necrosis and apoptosis, and decreases neutrophil aggregation. Zoniporide is applicable to research related to myocardial ischemia-reperfusion injury and heart graft ischemia-reperfusion injury .
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1
1 Cited Publications
Cat. No.: HY-106150B
CAS No.: 211813-86-4
Purity:  98.97%
Synonyms: EMD-96785 hydrochloride
Research Areas:  

Cardiovascular Disease

Eniporide hydrochloride (EMD-96785 hydrochloride) is a potent Na +/H + exchange inhibitor.
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Cat. No.: HY-P1769
CAS No.: 34233-50-6
Target:  

Angiotensin Receptor

Research Areas:  

Metabolic Disease Endocrinology

Angiotensin II (5-8), human is an endogenous C-terminal fragment of the peptide vasoconstrictor angiotensin II . Angiotensin II binds the AT II type 1 (AT1) receptor, stimulating GPCRs in vascular smooth muscle cells and increasing intracellular Ca 2+ levels. Angiotensin II also acts at the Na +/H + exchanger in the proximal tubules of the kidney .
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Cat. No.: HY-139313
CAS No.: 92434-13-4
Purity:  98.65%
Research Areas:  

Metabolic Disease

NHE3-IN-2 is a Na +/H + exchanger-3 (NHE3) inhibitor ( patent WO2001079186A1, example 6-Chlor-4-phenyl-2-chinazolinyl-guanidin) .
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Cat. No.: HY-N0150R
CAS No.: 22373-78-0
Synonyms: Monensin A sodium (Standard)
Monensin (sodium) (Standard) is the analytical standard of Monensin (sodium). This product is intended for research and analytical applications. Monensin (Monensin A) sodium, an orally active antibiotic, is an ionophore that mediates Na+/H+ exchange. Monensin sodium is a potent Wnt signaling inhibitor. Monensin sodium causes a marked enlargement of the multivesicular bodies (MVBs) and regulates exosome secretion. Monensin sodium can be used for bacterial, fungal, and parasitic infections research, and shows anticancer effects .
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Cat. No.: HY-19273R
CAS No.: 187870-78-6
Synonyms: EMD-87580 (Standard)
Rimeporide (Standard) is the analytical standard of Rimeporide. This product is intended for research and analytical applications. Rimeporide (EMD-87580) is a potent and selective inhibitor of the Na+/H+ exchanger (NHE-1).
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Cat. No.: HY-106150
CAS No.: 176644-21-6
Synonyms: EMD-96785
Eniporide (EMD 96785) is a Na(+)/H(+) exchange (NHE) inhibitor. Eniporide specifically inhibits the NHE-1 isoform. Eniporide improves cardiac performance inhibition associated with myocardial ischemia/reperfusion in animals, and limits infarct size in experimental models. Eniporide regulates cardiac performance and high-energy phosphate content in clinically relevant pig models of CPB and cardiac arrest .
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Cat. No.: HY-P1792
CAS No.: 52580-29-7
Target:  

Angiotensin Receptor

Research Areas:  

Metabolic Disease Endocrinology

Angiotensin II (1-4), human is an endogenous peptide produced from AT I by angiotensin-converting-enzyme (ACE). Angiotensin II binds the AT II type 1 (AT1) receptor, stimulating GPCRs in vascular smooth muscle cells and increasing intracellular Ca 2+ levels. Angiotensin II also acts at the Na +/H + exchanger in the proximal tubules of the kidney .
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Cat. No.: HY-105402
CAS No.: 339532-12-6
Research Areas:  

Cardiovascular Disease

T 162559 is a potent and selective inhibitor of the Na+/H+ exchanger isoform NHE1 with IC50 values of 0.96 nM. T 162559 does not affect Na+/HCO3- cotransport and Na+/Ca2+ exchange. T 162559 can be used for the research of cardiovascular disease .
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Cat. No.: HY-19062
CAS No.: 103898-38-0
SM-6586 is a calcium channel antagonist and inhibitor of Na +/H + and Na +/Ca 2+ exchange transport, potentially for the treatment of cerebrovasular diseases and hypertension.
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Cat. No.: HY-19273A
CAS No.: 187870-95-7
Synonyms: EMD-87580 hydrochloride
Research Areas:  

Metabolic Disease

Rimeporide hydrochloride (EMD-87580 hydrochloride) is a potent and selective inhibitor of the Na +/H + exchanger (NHE-1).
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Cat. No.: HY-177125
CAS No.: 1870822-78-8
Research Areas:  

Neurological Disease

Repunapanor (compound 123) is a potent Na+/H+ exchanger 3 (NHE-3) inhibitor .
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