Molecule Details
InChIKeyGKNPSSNBBWDAGH-UHFFFAOYSA-N
Canonical SMILESC[N+]1(C)CCCC(OC(=O)C(O)(c2ccccc2)c2ccccc2)C1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)2
Pfam Stratification Homologous
Avg pChEMBL8.68
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
DrugBank Annotations
DrugBank ID DB04843
Drug NameMepenzolate
CAS Number25990-43-6
Groups approved withdrawn
ATC Codes A03AB12
DescriptionMepenzolate is a post-ganglionic parasympathetic inhibitor. It decreases gastric acid and pepsin secretion and suppresses spontaneous contractions of the colon. Mepenzolate diminishes gastric acid and pepsin secretion. Mepenzolate also suppresses spontaneous contractions of the colon. Pharmacologica...

Categories: Acids, Carbocyclic Agents producing tachycardia Alimentary Tract and Metabolism Anticholinergic Agents Diphenylacetic Acids Drugs for Functional Gastrointestinal Disorders Hydroxy Acids Muscarinic Antagonists Phenylacetates Synthetic Anticholinergics, Quaternary Ammonium Compounds
Cross-references: BindingDB: 50377964 ChEBI: 94411 CHEMBL524004 ChemSpider: 3917 C07818 PharmGKB: PA164746250 PubChem:4057 PubChem:46508905 RxCUI: 107770 Therapeutic Targets Database: DAP001115 Wikipedia: Mepenzolate
Target Activities (2)
Target Gene Organism Category Pfam pChEMBL Type Source
P08172 CHRM2 Homo sapiens Human PF00001 8.9 Ki ChEMBL;BindingDB
P20309 CHRM3 Homo sapiens Human PF00001 8.4 Ki ChEMBL;BindingDB
DrugBank Target Actions (3)
Target Gene Target Name Action Type
P08912 CHRM5 Muscarinic acetylcholine receptor M5 antagonist targets
P11229 CHRM1 Muscarinic acetylcholine receptor M1 antagonist targets
P20309 CHRM3 Muscarinic acetylcholine receptor M3 antagonist targets