FR183998 free base is a potentNa⁺/H⁺-exchangeinhibitor, withIC₅₀s of 0.3 nM, 3.1 nM and 6.5 nM by measurement of pH_ichange in rat lymphocytes, rat and human platelets, respectively.

IC50: 0.3 nM (Na⁺/H⁺-exchange, Rat lymphocytes), 3.1 nM (Na⁺/H⁺-exchange, Human platelet), 6.5 nM (Na⁺/H⁺-exchange, Rat platelet)^[1]

FR183998 free base is a Na⁺/H⁺-exchange inhibitor, with IC₅₀s of 0.3 nM, 6.5 nM and 3.1 nM by measurement of pH_ichange in rat lymphocytes, rat and human platelets, respectively^[1].

FR183998 (0.1 and 1.0 mg/kg, i.v.) shows no effect hemodynamic parameters, and does not affect mean blood pressure and heart rate in conscious rats. Pretreatment of 0.01, 0.032, 0.10 mg/kg FR183998 or posttreament of 0.032 and 0.10 mg/kg FR183998 via intravenous administration, dose-dependently reuces reperfusion-induced ventricular fibrillation (VF) and mortality in reperfusion-induced arrhythmias in anesthetized rats, with ED₅₀s against VF of 0.015 mg/kg and 0.070 mg/kg, respectively. FR183998 also reduces myocardial infarct sizes, and suppresses the arrhythmias in anesthetized rats^[1]. FR183998 (1 mg/kg, i.v.) reduces the increase in serum levels of alanine transaminase, aspartate transaminase, and lactate dehydrogenase induced by hepatic I/R, and prevents the incidences of hepatic necrosis, apoptosis, and neutrophil infiltration. FR183998 blocks the I/R-induced activation of the NF-κB, reduces induction of iNOS and inhibits the production of nitric oxide. FR183998 also decreases the expression of the iNOS gene antisense transcript in the liver of hepatic I/R rats^[2].

428.34

Solid

C₁₇H₁₉Cl₂N₅O₂S

239440-20-1

Room temperature in continental US; may vary elsewhere.

DMSO : 250 mg/mL(583.65 mM;Need ultrasonic)

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