SML2767
HMR-1098
≥98% (HPLC)
别名:
5-chloro-2-methoxy-N-[2-[4-methoxy-3-[[[(methylamino)thioxomethyl]amino]sulfonyl]phenyl]ethyl]-benzamide sodium salt, HMR 1098
SMILES string
[Na]N(CCc2cc(c(cc2)OC)[S](=O)(=O)NC(=S)NC)C(=O)c1c(ccc(c1)Cl)OC
InChI
1S/C19H22ClN3O5S2.Na/c1-21-19(29)23-30(25,26)17-10-12(4-6-16(17)28-3)8-9-22-18(24)14-11-13(20)5-7-15(14)27-2;/h4-7,10-11H,8-9H2,1-3H3,(H3,21,22,23,24,29);/q;+1/p-1
InChI key
SUEVHDKFEXAKAF-UHFFFAOYSA-M
assay
≥98% (HPLC)
form
powder
storage condition
desiccated
color
white to beige
solubility
H2O: 2 mg/mL, clear
storage temp.
2-8°C
Quality Level
Biochem/physiol Actions
HMR-1098 is a potent and selective blocker of the sarcolemmal ATP-sensitive K+ (sarcKATP) channel. HMR 1098 is inhibits Kir6.2/SUR1-composed KATP channels.
potent and selective blocker of the sarcolemmal ATP-sensitive K+ (sarcKATP) channel
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Hai Xia Zhang et al.
Journal of molecular and cellular cardiology, 50(3), 552-560 (2010-12-28)
Murine ventricular and atrial ATP-sensitive potassium (K(ATP)) channels contain different sulfonylurea receptors (ventricular K(ATP) channels are Kir6.2/SUR2A complexes, while atrial K(ATP) channels are Kir6.2/SUR1 complexes). HMR 1098, the sodium salt of HMR 1883 {1-[[5-[2-(5-chloro-o-anisamido)ethyl]-2-methoxyphenyl]sulfonyl]-3-methylthiourea}, has been considered as a selective
Sergey Y Tsibulnikov et al.
General physiology and biophysics, 37(5), 537-547 (2018-10-12)
It was established that adaptation to chronic continuous normobaric hypoxia (CCNH) increases cardiac tolerance to ischemia and reperfusion. It was performed coronary artery occlusion (20 min) and reperfusion (3 h) in Wistar rats. CCNH promoted a decrease in the infarct
Xiaohui Zhang et al.
International journal of molecular medicine, 38(3), 758-766 (2016-07-20)
The sarcolemmal ATP-sensitive K+ (sarcKATP) channel plays a cardioprotective role during stress. However, the role of the sarcKATP channel in the apoptosis of cardiomyocytes and association with mitochondrial calcium remains unclear. For this purpose, we developed a model of LPS-induced sepsis
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