Drug Information
Drug General Information | Top | |||
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Drug ID |
D0B7YT
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Former ID |
DAP000343
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Drug Name |
Scopolamine
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Synonyms |
Atroscine; Euscopol; Hyosceine; Hysco; Isoscopil; Kwells; SEE; Scop; Scopamin; Scopolaminhydrobromid; Scopos; Sereen; Tranaxine; Transcop; Triptone; Atroscine Hydrobromide; Hydroscine hydrobromide; Hyocine F hydrobromide; Hyoscine bromide; Hyoscyine hydrobromide; SCOPOLAMINE BROMIDE; Scopolamine Hyoscine; Scopolaminium bromide; Scopolammonium bromide; Tropane alkaloid; MOLI001381; NCI61806; Borrachero (TN); Burundanga (TN); Hyoscine (TN); L-Hyoscine hydrobromide; Scopoderm-TTS; Scopolamine (INN); Transderm scop (TN); Levo-duboisine (TN); Xy-, (-)-tropate (ester); (-)-Scopolamine hydrobromide trihydrate; 1alphaH,5alphaH-Tropan-3alpha-ol, 6beta,7beta-epo; 1alphaH,5alphaH-Tropan-3alpha-ol, 6beta,7beta-epoxy-, (-)-tropate (ester); 3-Oxa-9-azatricyclo(3.3.1.O(sup 2,4))nonan-7-ol, 9-methyl-, tropate (ester); 9-methyl-3-oxa-9-azatricyclo[3.3.1.0~2,4~]non-7-yl tropate
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Drug Type |
Small molecular drug
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Indication | Addictive disorder [ICD-11: 6C50-6C5Z] | Approved | [1], [2] | |
Nausea [ICD-11: MD90; ICD-10: R11] | Approved | [1], [2] | ||
Therapeutic Class |
Antispasmodics
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Company |
Norvatis Phamaceuticals Corporation
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Structure |
Download2D MOL |
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Formula |
C17H21NO4
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Canonical SMILES |
CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4
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InChI |
1S/C17H21NO4/c1-18-13-7-11(8-14(18)16-15(13)22-16)21-17(20)12(9-19)10-5-3-2-4-6-10/h2-6,11-16,19H,7-9H2,1H3/t11?,12-,13-,14+,15-,16+/m1/s1
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InChIKey |
STECJAGHUSJQJN-USLFZFAMSA-N
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CAS Number |
CAS 114-49-8
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PubChem Compound ID | ||||
PubChem Substance ID | ||||
ChEBI ID |
CHEBI:16794
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ADReCS Drug ID | BADD_D01994 ; BADD_D01995 | |||
SuperDrug ATC ID |
A04AD01; N05CM05; S01FA02
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SuperDrug CAS ID |
cas=000051343
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Target and Pathway | Top | |||
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Target(s) | Muscarinic acetylcholine receptor (CHRM) | Target Info | Antagonist | [3], [4] |
KEGG Pathway | Calcium signaling pathway | |||
cAMP signaling pathway | ||||
Neuroactive ligand-receptor interaction | ||||
PI3K-Akt signaling pathway | ||||
Cholinergic synapse | ||||
Regulation of actin cytoskeleton | ||||
Pathwhiz Pathway | Muscle/Heart Contraction | |||
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 | ||||
Secretion of Hydrochloric Acid in Parietal Cells | ||||
GPCR ligand binding | ||||
GPCR downstream signaling |
References | Top | |||
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REF 1 | URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 330). | |||
REF 2 | Drug Information of Calcidiol from nextbio research in illumina. 2015. | |||
REF 3 | The amygdala modulates morphine-induced state-dependent memory retrieval via muscarinic acetylcholine receptors. Neuroscience. 2009 May 5;160(2):255-63. | |||
REF 4 | Midbrain acetylcholine and glutamate receptors modulate accumbal dopamine release. Neuroreport. 2008 Jun 11;19(9):991-5. |
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