Drug Information
Drug General Information | Top | |||
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Drug ID |
D09STY
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Drug Name |
PMID29334795-Compound-55
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Drug Type |
Small molecular drug
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Company |
TAKEDA PHARMACEUTICAL COMPANY LIMITED RUPRAH, Parminder, Kaur MERCHANT, Kevin, John WALSH, Louise, Marie KERR, Catrina, Morven FIELDHOUSE, Charlotte HARRISSON, David MAINE, Stephanie HAZEL, Katherine
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Structure |
Download2D MOL |
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Formula |
C24H35NO2
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Canonical SMILES |
COC1CCC(CC1)(C2=CC=C(C=C2)C=C3CCCN(CC3)C4CCC4)O
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InChI |
1S/C24H35NO2/c1-27-23-11-14-24(26,15-12-23)21-9-7-20(8-10-21)18-19-4-3-16-25(17-13-19)22-5-2-6-22/h7-10,18,22-23,26H,2-6,11-17H2,1H3/b19-18+
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InChIKey |
CVCLZBKTZVQEGU-VHEBQXMUSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Histamine H3 receptor (H3R) | Target Info | . | [1] |
Target's Patent Info | Histamine H3 receptor (H3R) | Target's Patent Info | [1] | |
KEGG Pathway | Neuroactive ligand-receptor interaction | |||
Reactome | Histamine receptors | |||
G alpha (i) signalling events | ||||
WikiPathways | Monoamine Transport | |||
GPCRs, Class A Rhodopsin-like | ||||
GPCR ligand binding | ||||
GPCR downstream signaling |
References | Top | |||
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REF 1 | Progress in the development of histamine H3 receptor antagonists/inverse agonists: a patent review (2013-2017).Expert Opin Ther Pat. 2018 Mar;28(3):175-196. |
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