Drotaverine hydrochloride is a selective phosphodiesterase type 4 (PDE4) inhibitor, which effectively prevents the degradation of 3',5'-cyclic adenosine monophosphate (cAMP). This compound demonstrates notable antispasmodic activity in vivo while avoiding anticholinergic side effects. Due to its mechanism of action, Drotaverine hydrochloride is valuable for research involving smooth muscle relaxation and the modulation of cAMP-related cellular pathways.
Drotaverine hydrochloride is a selective phosphodiesterase type 4 (PDE4) inhibitor, which effectively prevents the degradation of 3',5'-cyclic adenosine monophosphate (cAMP). This compound demonstrates notable antispasmodic activity in vivo while avoiding anticholinergic side effects. Due to its mechanism of action, Drotaverine hydrochloride is valuable for research involving smooth muscle relaxation and the modulation of cAMP-related cellular pathways.
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