Drug Information
Drug General Information | Top | |||
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Drug ID |
D0O8AQ
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Former ID |
DNC010354
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Drug Name |
Isosorbide-di-(ethylcarbamate)
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Synonyms |
Isosorbide-di-(ethylcarbamate); CHEMBL600621; BDBM50306694
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Drug Type |
Small molecular drug
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Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
Structure |
Download2D MOL |
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Formula |
C12H20N2O6
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Canonical SMILES |
CCNC(=O)OC1COC2C1OCC2OC(=O)NCC
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InChI |
1S/C12H20N2O6/c1-3-13-11(15)19-7-5-17-10-8(6-18-9(7)10)20-12(16)14-4-2/h7-10H,3-6H2,1-2H3,(H,13,15)(H,14,16)/t7-,8+,9-,10-/m1/s1
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InChIKey |
IMAKVWCOCNQBSI-UTINFBMNSA-N
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PubChem Compound ID |
Target and Pathway | Top | |||
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Target(s) | Acetylcholinesterase (AChE) | Target Info | Inhibitor | [1] |
Cholinesterase (BCHE) | Target Info | Inhibitor | [1] | |
KEGG Pathway | Glycerophospholipid metabolism | |||
Cholinergic synapse | ||||
Panther Pathway | Muscarinic acetylcholine receptor 1 and 3 signaling pathway | |||
Muscarinic acetylcholine receptor 2 and 4 signaling pathway | ||||
Nicotinic acetylcholine receptor signaling pathway | ||||
Pathwhiz Pathway | Phospholipid Biosynthesis | |||
Pathway Interaction Database | ATF-2 transcription factor network | |||
WikiPathways | Irinotecan Pathway | |||
Monoamine Transport | ||||
Biogenic Amine Synthesis | ||||
Acetylcholine Synthesis | ||||
Integrated Pancreatic Cancer Pathway |
References | Top | |||
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REF 1 | Isosorbide-based cholinesterase inhibitors; replacement of 5-ester groups leading to increased stability. Bioorg Med Chem. 2010 Feb;18(3):1045-53. |
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