SB 239063 5 mg | 99.81%
TargetMol

SB239063 is a potent and selective p38 MAPKα/β inhibitor with IC50 of 44 nM, showing no activity against the γ- and δ-kinase isoforms.
More Information Supplier PageSB239063 is a potent and selective p38 MAPKα/β inhibitor with IC50 of 44 nM, showing no activity against the γ- and δ-kinase isoforms.
More Information Supplier PageZM-241385 is a high-affinity antagonist ligand selective for the adenosine A2A receptor.
More Information Supplier PageZM-241385 is a high-affinity antagonist ligand selective for the adenosine A2A receptor.
More Information Supplier PageChlorprothixene is a typical antipsychotic drug of the thioxanthene class, which was the first of the series to be synthesized.
More Information Supplier PageChlorprothixene is a typical antipsychotic drug of the thioxanthene class, which was the first of the series to be synthesized.
More Information Supplier PageDomperidone(Motilium) is a dopamine blocker and an antidopaminergic reagent. It blocks the action of. It has strong affinities for the D2 and D3 dopamine receptors, which are found in the chemoreceptor trigger zone, located just outside the blood brain barrier, which – among others – regulates nausea and vomiting (area postrema on the floor of […]
More Information Supplier PageDomperidone(Motilium) is a dopamine blocker and an antidopaminergic reagent. It blocks the action of. It has strong affinities for the D2 and D3 dopamine receptors, which are found in the chemoreceptor trigger zone, located just outside the blood brain barrier, which – among others – regulates nausea and vomiting (area postrema on the floor of […]
More Information Supplier PageMirtazapine is a tetracyclic antidepressant with a somewhat unique mechanism of action. Mirtazapine therapy can be associated with transient asymptomatic elevations in serum aminotransferase levels and has been linked to rare instances of clinically apparent acute liver injury.
More Information Supplier PageZalcitabine(Dideoxycytidine;ddC; 2′, 3′-Dideoxycytidine) is a nucleoside analog reverse transcriptase inhibitor (NRTI); At low concentrations, It can potently inhibit HIV replication by binding to reverse transcriptase terminated synthesis of viral DNA chain.
More Information Supplier PageZalcitabine(Dideoxycytidine;ddC; 2′, 3′-Dideoxycytidine) is a nucleoside analog reverse transcriptase inhibitor (NRTI); At low concentrations, It can potently inhibit HIV replication by binding to reverse transcriptase terminated synthesis of viral DNA chain.
More Information Supplier Page