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Drotaverine hydrochloride
CAS No. : 985-12-6
Biological Activity：Drotaverine (hydrochloride) is a type 4 cyclic nucleotide phosphodiesterase (PDE4) inhibitor and an L-type voltage-dependent calcium channel (L-VDCC) blocker, blocks the degradation of 3′,5′-cyclic adenosine monophosphate. Drotaverine (hydrochloride) exhibits in vivo antispasmodic efficacy without anticholinergic effects.
Targets：Phosphodiesterase (PDE)|Calcium Channel
Related Screening Libraries:Natural Product-like Compound Library;Drug Repurposing Compound Library Plus;FDA-Approved Drug Library Plus;FDA-Approved Drug Library Mini;Bioactive Compound Library Plus;Membrane Transporter/Ion Channel Compound Library;Metabolism/Protease Compound Library;Neuronal Signaling Compound Library;FDA-Approved Drug Library;Drug Repurposing Compound Library;NMPA-Approved Drug Library;FDA Approved & Pharmacopeial Drug Library;Anti-Alzheimer’s Disease Compound Library;Neuroprotective Compound Library;Neurodegenerative Disease-related Compound Library;Mechanoreceptors Compound Library;Anti-Colorectal Cancer Compound Library ;Antidepressant Compound Library;Calcium Channel Blocker Library;Human Metabolite Library;
Related Small Molecules:Senazodan hydrochloride;(E/Z)-HA155;Enpp/Carbonic anhydrase-IN-1;Benidipine hydrochloride;ATX inhibitor 22;CaV1.3 antagonist-1;14-Deoxyandrographolide;Carbazeran citrate;Bay 60-7550;BC11-38;(Rac)-MEM 1003;Deltarasin hydrochloride;Glaucine;Efonidipine hydrochloride monoethanolate;L-Ascorbic acid sodium salt;Brompheniramine-d6 maleate;MRS 1523;Nilvadipine;Ziritaxestat;Udenafil-d7;D159687;Lercanidipine;ITI-214;CP-060;PDE10-IN-5
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