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Medchemexpress LLC Drotaverine (hydrochloride) | 985-12-6 | 99.65% | 433.97 | 25 MG
SDP

Catalog No. 5000347275
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Drotaverine hydrochloride is a type 4 cyclic nucleotide phosphodiesterase (PDE4) inhibitor and an L-type voltage-dependent calcium channel (L-VDCC) blocker, which blocks the degradation of 3',5'-cyclic adenosine monophosphate. It exhibits in vivo antispasmodic efficacy without anticholinergic effects.

  • Type 4 cyclic nucleotide phosphodiesterase (PDE4) inhibitor
  • L-type voltage-dependent calcium channel (L-VDCC) blocker
  • Blocks the degradation of 3',5'-cyclic adenosine monophosphate
  • Exhibits in vivo antispasmodic efficacy without anticholinergic effects
  • Relaxant for pre-contracted airways
  • Suppresses bronchial contractions in guinea pigs
  • Shows higher selectivity for KCl-induced contractions
  • Improves cognitive impairment and regulates levels of neurotransmitters in the brain in animal models

Catalog No. 50-003-47275 Supplier Medchemexpress LLC Supplier No. 25MGHY108974
May include imposed supplier surcharges.
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Drotaverine hydrochloride is a type 4 cyclic nucleotide phosphodiesterase (PDE4) inhibitor and an L-type voltage-dependent calcium channel (L-VDCC) blocker, which blocks the degradation of 3',5'-cyclic adenosine monophosphate. It exhibits in vivo antispasmodic efficacy without anticholinergic effects.

  • Type 4 cyclic nucleotide phosphodiesterase (PDE4) inhibitor
  • L-type voltage-dependent calcium channel (L-VDCC) blocker
  • Blocks the degradation of 3',5'-cyclic adenosine monophosphate
  • Exhibits in vivo antispasmodic efficacy without anticholinergic effects
  • Relaxant for pre-contracted airways
  • Suppresses bronchial contractions in guinea pigs
  • Shows higher selectivity for KCl-induced contractions
  • Improves cognitive impairment and regulates levels of neurotransmitters in the brain in animal models

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