10 Results for "

SUR2

" in MedChemExpress (MCE) Product Catalog:
Products (10)

10 Results for "SUR2" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-108573
CAS No.: 60559-98-0
Purity:  99.81%
Target:  

Potassium Channel

연구분야:  

Cardiovascular Disease

P-1075 is a potent activator of sulfonylurea receptor 2-associated ATP-sensitive potassium channels (SUR2-KIR6), with an EC50 value of 45 nM for SUR2B-KIR6 channel activation . P-1075 also P1075 opens mitochondrial K(ATP) channels and generates reactive oxygen species resulting in cardioprotection of rabbit hearts [2].
Cat. No.: HY-162322
CAS No.: 1396814-79-1
Target:  

Potassium Channel

연구분야:  

Cardiovascular Disease

VU0542270 is a selective vascular Kir6.1/SUR2B KATP channel inhibitor with an IC50 value of 100 nM. VU0542270 has an IC50 > 30 μM for the other nine members of the Kir channel family. VU0542270 can be used in the study of cardiovascular disease .
Cat. No.: HY-108573R
CAS No.: 60559-98-0
Target:  

Potassium Channel

연구분야:  

Cardiovascular Disease

P-1075 (Standard) is the analytical standard of P-1075. This product is intended for research and analytical applications. P-1075 is a potent activator of sulfonylurea receptor 2-associated ATP-sensitive potassium channels (SUR2-KIR6), with an EC50 value of 45 nM for SUR2B-KIR6 channel activation . P-1075 also P1075 opens mitochondrial K(ATP) channels and generates reactive oxygen species resulting in cardioprotection of rabbit hearts [2].
Cat. No.: HY-120158
CAS No.: 172649-40-0
Target:  

Potassium Channel

연구분야:  

Neurological Disease

ZD0947 is an ATP-sensitive potassium channel activator with relatively effective activation of smooth muscle KATP channels (SUR2B/Kir6.1 and SUR2B/Kir6.2). ZD0947 partially antagonizes pancreatic KATP channels (SUR1/Kir6.2) and cardiac KATP channels (SUR2A/Kir6.2). ZD0947 is potentially used to inhibit overactive bladder (OAB) .
Cat. No.: HY-W740628
CAS No.: 107833-98-7
Target:  

Drug Metabolite

연구분야:  

Neurological Disease

Nicorandil pyridine oxide is a metabolite of the sulfonylurea receptor 2B (SUR2B) linked to ATP-sensitive potassium channel Kir6.2 (SUR2B/Kir6.2) activator and nitric oxide donor Nicorandil.
Cat. No.: HY-RS08294
연구분야:  

Others

MED23 Human Pre-designed siRNA Set A contains three designed siRNAs for MED23 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

Cat. No.: HY-RS22364
연구분야:  

Others

Abcc9 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Abcc9 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

Cat. No.: HY-RS00067
연구분야:  

Others

ABCC9 Human Pre-designed siRNA Set A contains three designed siRNAs for ABCC9 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

Cat. No.: HY-15210
CAS No.: 54870-28-9
Target:  

Potassium Channel

연구분야:  

Metabolic Disease

Meglitinide is an ATP-sensitive potassium (KATP) channel inhibitor. Meglitinide exhibits IC50 values of 0.26 μM, 0.53 μM and 1.6 μM against KATP channels containing SUR1, SUR2A and SUR2B, respectively, with a Kd value of 7 μM for both SUR1 and SUR2A, and a Kd value of 8 μM for SUR2B. Meglitinide binds to the SUR1, SUR2A and SUR2B subunits with high affinity to close KATP channels, acting on a binding site shared by all SUR subtypes, and its interaction with SUR1 carrying the S1237Y mutation remains unchanged. Meglitinide is applicable to research related to type 2 diabetes .
Cat. No.: HY-RS28888
연구분야:  

Others

Abcc9 Rat Pre-designed siRNA Set A contains three designed siRNAs for Abcc9 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.