28 Results for "

NaH

" in MedChemExpress (MCE) Product Catalog:
Products (28)

28 Results for "NaH" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-P701153
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: NHERF1; Solute Carrier Family 9 Isoform A3 Regulatory Factor 1; Prev. SLC9A3R1; Na(+)/H(+) Exchange Regulatory Cofactor 1; NHERF-1; SLC9A3 Regulator 1; NHERF; Solute Carrier Family 9 (Sodium/Hydrogen Exchanger), Isoform 3 Regulatory Factor 1; EBP50; Solut
Species:  
Source:  
loading...
    loading...
Cat. No.: HY-160113
Sodium phosphate buffer 0.02 M, pH 6.9 is a commonly used aqueous biological buffer that maintains a stable pH value. Sodium phosphate buffer 0.02 M, pH 6.9 is often used in enzyme activity assays, such as α-amylase assays. Sodium phosphate buffer 0.02 M, pH 6.9 is prepared by mixing disodium hydrogen phosphate (Na2HPO4) (HY-B2243) and sodium dihydrogen phosphate (NaH2PO4) (HY-Y0308) to a total concentration of 0.02 M .
loading...
    loading...
Cat. No.: HY-160113B
Sodium phosphate buffer 0.1M, pH 6.8 is mainly composed of two phosphates, Na2HPO4 and NaH2PO4, with a total phosphate concentration of 0.1 M, which mainly acts as a buffer in the reaction.
loading...
    loading...
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 .
loading...
    loading...
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).
loading...
    loading...
Cat. No.: HY-W002718
CAS No.: 16063-69-7
Research Areas:  

Others

2,4,6-Trichloropyridine is a trichloro-substituted nitrogen-containing heterocyclic compound that serves as an intermediate for studies related to organic synthesis. 2,4,6-Trichloropyridine reacts with n-BuLi to form a stable 3-lithiated pyridine intermediate .
loading...
    loading...
Cat. No.: HY-160113D
Sodium phosphate buffer 0.1M, pH 7.5 is mainly composed of two phosphates, Na2HPO4 and NaH2PO4, with a total phosphate concentration of 0.1 M, which mainly acts as a buffer in the reaction.
loading...
    loading...
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 .
loading...
    loading...
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 .
loading...
    loading...
Cat. No.: HY-160113C
Sodium phosphate buffer 0.1M, pH 7.2 is mainly composed of two phosphates, Na2HPO4 and NaH2PO4, with a total phosphate concentration of 0.1 M, which mainly acts as a buffer in the reaction.
loading...
    loading...
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 .
loading...
    loading...
Cat. No.: HY-123679
CAS No.: 168620-46-0
FR168888 is an inhibitor of Na+/H+ exchange with a Ki value of 6.4 nM .
loading...
    loading...
Cat. No.: HY-163365
Research Areas:  

Cancer

UTX-143 is an inhibitor of Na+/H+ exchange protein (NHE5). UTX-143 has antitumor activity .
loading...
    loading...
Cat. No.: HY-153719
CAS No.: 40420-48-2
Target:  

SARS-CoV

Research Areas:  

Infection

NSC111552 is a potent SARS-CoV-2 NSP14 MTase inhibitor. NSC111552 inhibits the FL-NAH binding to the SARS-CoV-2 NSP14 MTase with an IC50 of 5.1 μM .
loading...
    loading...
Cat. No.: HY-13412
CAS No.: 159138-81-5
Synonyms: HOE-642
Research Areas:  

Cardiovascular Disease

Cariporide is a Na+/H+ Exchanger 1 (NHE-1) inhibitor. Cariporide inhibits the expression of monocyte endothelial cell adhesion and intercellular adhesion molecule-1 (ICAM-1) mediated by high glucose (HG) by inhibiting the activation of NHE-1 .
loading...
    loading...
Cat. No.: HY-106150A
CAS No.: 190368-98-0
Research Areas:  

Cardiovascular Disease

Eniporide mesylate (EMD 96785 mesylate) is a Na(+)/H(+) exchange (NHE) inhibitor. Eniporide mesylate specifically inhibits the NHE-1 isoform. Eniporide mesylate improves cardiac performance inhibition associated with myocardial ischemia/reperfusion in animals, and limits infarct size in experimental models. Eniporide mesylate regulates cardiac performance and high-energy phosphate content .
loading...
    loading...
Cat. No.: HY-162680
Target:  

Influenza Virus

Research Areas:  

Infection

OSC-GCDI(P) is a broad-spectrum orally active anti-influenza virus agent that exhibits significant inhibitory effects against both wild-type and Oseltamivir (HY-13317) resistant (H275Y) influenza virus strains in mouse infection models. OSC-GCDI(P) is capable of preventing not only wild-type influenza viruses but also OS-resistant variants with NA(H275Y) .
loading...
    loading...
Cat. No.: HY-100490S
CAS No.: 85047-14-9
Rilmenidine-d4 is the deuterium labeled Rilmenidine. Rilmenidine, an innovative antihypertensive agent, is an orally active, selective I1 imidazoline receptor agonist. Rilmenidine is an alpha 2-adrenoceptor agonist. Rilmenidine induces autophagy. Rilmenidine acts both centrally by reducing sympathetic overactivity and in the kidney by inhibiting the Na+/H+ antiport. Rilmenidine modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells .
loading...
    loading...
Cat. No.: HY-100490BR
CAS No.: 85409-38-7
Rilmenidine (phosphate) (Standard) is the analytical standard of Rilmenidine (phosphate). This product is intended for research and analytical applications. Rilmenidine phosphate, an innovative antihypertensive agent, is an orally active, selective I1 imidazoline receptor agonist. Rilmenidine phosphate is an alpha 2-adrenoceptor agonist. Rilmenidine phosphate induces autophagy. Rilmenidine phosphate acts both centrally by reducing sympathetic overactivity and in the kidney by inhibiting the Na+/H+ antiport. Rilmenidine phosphate modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells .
loading...
    loading...
Cat. No.: HY-100490R
CAS No.: 54187-04-1
Rilmenidine (Standard) is the analytical standard of Rilmenidine. This product is intended for research and analytical applications. Rilmenidine, an innovative antihypertensive agent, is an orally active, selective I1 imidazoline receptor agonist. Rilmenidine is an alpha 2-adrenoceptor agonist. Rilmenidine induces autophagy. Rilmenidine acts both centrally by reducing sympathetic overactivity and in the kidney by inhibiting the Na+/H+ antiport. Rilmenidine modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells .
loading...
    loading...