Chlorothiazide

The Exaxol 0.04% chlorophenol red aqueous solution is mainly used in research facilities and chemical laboratories to conduct wide range of experiments.

The Exaxol 0.04% chlorophenol red aqueous solution is mainly used in research facilities and chemical laboratories to conduct wide range of experiments.

A macrolide-type antibiotic that inhibits pyruvate carboxylases from Bacillus, Azotobacter, rat, and chicken (Ki or IC₅₀ = 173, 500, 260, and 120 &muM, respectively) also inhibits MDH1 (cytoplasmic) and MDH2 (mitochondrial)

A derivative of hydrochlorothiazide, which is a diuretic and antihypertensive agent that increases renal excretion of sodium, potassium, chloride, and bicarbonate ions by inhibiting tubular reabsorptive mechanisms.

The hydrochloride of leelamine, an inhibitor of pyruvate dehydrogenase kinase.

An antihistamine that antagonizes the H1 receptor at high nanomolar concentrations less potently blocks TRPC5 (IC₅₀ = 1.0-1.3 &microM), with at least 6-fold selectivity for TRPC5 over other TRP channels.

A potent, selective agonist of the adenosine A2A receptor (Ki = 11-46 nM) less effective at adenosine A1 and A3 receptors (Kis = 0.5-3.1 and 0.6-1 &microM, respectively) and is without effect at adenosine A2B (Ki &gt 10 &microM).

A long-lasting antagonist of nAChRs and ganglion blocker.

The hydrochloride of leelamine, an inhibitor of pyruvate dehydrogenase kinase.

A derivative of hydrochlorothiazide, which is a diuretic and antihypertensive agent that increases renal excretion of sodium, potassium, chloride, and bicarbonate ions by inhibiting tubular reabsorptive mechanisms.

A macrolide-type antibiotic that inhibits pyruvate carboxylases from Bacillus, Azotobacter, rat, and chicken (Ki or IC₅₀ = 173, 500, 260, and 120 &muM, respectively) also inhibits MDH1 (cytoplasmic) and MDH2 (mitochondrial)

A histamine H1 receptor antagonist (Ki = 9 nM) that is effective against HCV (EC₅₀ = 44 nM), preventing viral entry into host cells.