Drug Information
Drug General Information | |||||
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Drug ID |
D04YEW
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Former ID |
DIB005258
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Drug Name |
Tarafenacin
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Synonyms |
SVT-40776; Muscarinic M3 receptor antagonist (overactive bladder), SALVAT
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Drug Type |
Small molecular drug
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Indication | Overactive bladder disorder [ICD9: 188, 596.51; ICD10:C67, N32.81] | Phase 2 | [1] | ||
Company |
Laboratorios SALVAT SA
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Structure |
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Download2D MOL |
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Formula |
C21H20F4N2O2
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Canonical SMILES |
C1N2CC[C@@H]([C@H]1OC(=O)N(c1cc(ccc1)F)Cc1cc(c(c(c1)F)F<br />)F)CC2
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CAS Number |
CAS 385367-47-5
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Muscarinic acetylcholine receptor M3 | Target Info | Antagonist | [2] | |
KEGG Pathway | Calcium signaling pathway | ||||
Neuroactive ligand-receptor interaction | |||||
Cholinergic synapse | |||||
Regulation of actin cytoskeleton | |||||
Insulin secretion | |||||
Salivary secretion | |||||
Gastric acid secretion | |||||
Pancreatic secretion | |||||
PANTHER Pathway | Alzheimer disease-amyloid secretase pathway | ||||
Heterotrimeric G-protein signaling pathway-Gq alpha and Go alpha mediated pathway | |||||
Muscarinic acetylcholine receptor 1 and 3 signaling pathway | |||||
PathWhiz Pathway | Gastric Acid Production | ||||
Reactome | Muscarinic acetylcholine receptors | ||||
Acetylcholine regulates insulin secretion | |||||
G alpha (q) signalling events | |||||
WikiPathways | Monoamine GPCRs | ||||
Calcium Regulation in the Cardiac Cell | |||||
Regulation of Actin Cytoskeleton | |||||
GPCRs, Class A Rhodopsin-like | |||||
Gastrin-CREB signalling pathway via PKC and MAPK | |||||
Integration of energy metabolism | |||||
GPCR ligand binding | |||||
GPCR downstream signaling | |||||
GPCRs, Other | |||||
References | |||||
REF 1 | ClinicalTrials.gov (NCT01458197) A Phase 2 Study to Compare the Efficacy and Tolerability of Tarafenacin 0.2 mg and Tarafenacin 0.4 mg to Placebo in Patients Suffering From Overactive Bladder.. U.S. National Institutes of Health. | ||||
REF 2 | In vivo and in vitro pharmacological characterization of SVT-40776, a novel M3 muscarinic receptor antagonist, for the treatment of overactive bladder. Br J Pharmacol. 2009 Mar;156(5):807-17. | ||||
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