Drug Information
| Drug General Information | Top | |||
|---|---|---|---|---|
| Drug ID |
D0PF3Z
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| Former ID |
DNC013768
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| Drug Name |
N-isopropylnorlitebamineN-methoiodide
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| Synonyms |
N-isopropylnorlitebamineN-methoiodide
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent [ICD-11: N.A.] | Investigative | [1] | |
| Structure |
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Download2D MOL |
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| Formula |
C23H28INO4
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| Canonical SMILES |
CCC[N+]1(CCC2=C3C=CC4=CC(=C(C=C4C3=C(C(=C2C1)O)OC)OC)O)C.[I-]
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| InChI |
1S/C23H27NO4.HI/c1-5-9-24(2)10-8-15-16-7-6-14-11-19(25)20(27-3)12-17(14)21(16)23(28-4)22(26)18(15)13-24;/h6-7,11-12H,5,8-10,13H2,1-4H3,(H-,25,26);1H
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| InChIKey |
ATOFDXKLKQOFOQ-UHFFFAOYSA-N
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| PubChem Compound ID | ||||
| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Acetylcholinesterase (AChE) | 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 | Monoamine Transport | |||
| Biogenic Amine Synthesis | ||||
| Acetylcholine Synthesis | ||||
| Integrated Pancreatic Cancer Pathway | ||||
| References | Top | |||
|---|---|---|---|---|
| REF 1 | Litebamine N-homologues: preparation and anti-acetylcholinesterase activity. J Nat Prod. 1998 Jan;61(1):46-50. | |||
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