Drug Information
Drug General Information | |||||
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Drug ID |
D08YVT
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Former ID |
DNC004557
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Drug Name |
SCH-211803
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Drug Type |
Small molecular drug
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Indication | Parkinson's disease [ICD9: 332; ICD10:G20] | Discontinued in Phase 1 | [1] | ||
Structure |
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Download2D MOL |
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Formula |
C31H36ClN3O3S
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Canonical SMILES |
CC1=CC=CC(=C1N)C(=O)N2CCC(CC2)N3CCC(CC3)CC4=CC=C(C=C4)S<br />(=O)(=O)C5=CC(=CC=C5)Cl
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InChI |
1S/C31H36ClN3O3S/c1-22-4-2-7-29(30(22)33)31(36)35-18-14-26(15-19-35)34-16-12-24(13-17-34)20-23-8-10-27(11-9-23)39(37,38)28-6-3-5-25(32)21-28/h2-11,21,24,26H,12-20,33H2,1H3
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InChIKey |
VMJKUCKTXMESQR-UHFFFAOYSA-N
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PubChem Compound ID | |||||
Target and Pathway | |||||
Target(s) | Muscarinic acetylcholine receptor M2 | Target Info | Inhibitor | [2] | |
KEGG Pathway | Calcium signaling pathway | ||||
cAMP signaling pathway | |||||
Neuroactive ligand-receptor interaction | |||||
PI3K-Akt signaling pathway | |||||
Cholinergic synapse | |||||
Regulation of actin cytoskeleton | |||||
PANTHER Pathway | Alzheimer disease-amyloid secretase pathway | ||||
Heterotrimeric G-protein signaling pathway-Gi alpha and Gs alpha mediated pathway | |||||
Heterotrimeric G-protein signaling pathway-Gq alpha and Go alpha mediated pathway | |||||
Muscarinic acetylcholine receptor 2 and 4 signaling pathway | |||||
PathWhiz Pathway | Muscle/Heart Contraction | ||||
Reactome | Muscarinic acetylcholine receptors | ||||
G alpha (i) signalling events | |||||
WikiPathways | SIDS Susceptibility Pathways | ||||
Monoamine GPCRs | |||||
Calcium Regulation in the Cardiac Cell | |||||
Regulation of Actin Cytoskeleton | |||||
GPCRs, Class A Rhodopsin-like | |||||
GPCR ligand binding | |||||
GPCR downstream signaling | |||||
GPCRs, Other | |||||
References | |||||
REF 1 | Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800015639) | ||||
REF 2 | J Med Chem. 2002 Dec 5;45(25):5415-8.Improving the oral efficacy of CNS drug candidates: discovery of highly orally efficacious piperidinyl piperidine M2 muscarinic receptor antagonists. | ||||
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