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BOC Sciences |
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1-631-485-4226; 16314854226 |
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info@bocsci.com |
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| | FR183998 free base Basic information |
| Product Name: | FR183998 free base | | Synonyms: | FR183998 free base;1,3-Benzenedicarboxamide, N1-(aminoiminomethyl)-5-(2,5-dichloro-3-thienyl)-N3-[2-(dimethylamino)ethyl]-;FR-183998 free base,FR183998 free base;FR183998 | | CAS: | 239440-20-1 | | MF: | C17H19Cl2N5O2S | | MW: | 428.34 | | EINECS: | | | Product Categories: | | | Mol File: | 239440-20-1.mol |  |
| | FR183998 free base Chemical Properties |
| density | 1.48±0.1 g/cm3(Predicted) | | storage temp. | Store at -20°C | | solubility | Soluble in DMSO | | form | Solid | | pka | 11.35±0.46(Predicted) | | color | White to off-white |
| | FR183998 free base Usage And Synthesis |
| Uses | FR183998, is a potent Na+/H+-exchange inhibitor. | | in vivo | 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]. |
| | FR183998 free base Preparation Products And Raw materials |
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