Drug intelligence / Profile preview

drotaverine (Adorshea Bioceutics)

Development stage
Unknown
Lead developer
Adorshea Bioceutics
Modality
Small Molecules
Administration
Oral
01

Overview

Drotaverine is a benzylisoquinoline derivative and a potent antispasmodic agent. It acts as a selective inhibitor of the enzyme phosphodiesterase 4 (PDE4), which leads to an increase in intracellular levels of cyclic adenosine monophosphate (cAMP) in smooth muscle cells. This mechanism results in the relaxation of smooth muscles across various organ systems, including the gastrointestinal, biliary, and urogenital tracts, as well as the uterus. Marketed by Adorshea Bioceutics under the brand name Adorta, it is primarily indicated for the relief of smooth muscle spasms and is also utilized in obstetric care for the management of preterm labor to facilitate cervical dilation. Unlike some other antispasmodics, drotaverine does not possess anticholinergic properties, which reduces the incidence of side effects such as dry mouth or blurred vision.

Brand names
Adorta
Other names
drotaverine hydrochloride
02

Targets

PDE4 (Phosphodiesterase 4A1)LTCC (Voltage-gated calcium channel (L-type))PDE (Phosphodiesterase family)Acetylcholinesterase

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