Drug Information
| Drug General Information | |||||
|---|---|---|---|---|---|
| Drug ID |
D0PF3Z
|
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| Former ID |
DNC013768
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| Drug Name |
N-isopropylnorlitebamineN-methoiodide
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| Drug Type |
Small molecular drug
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| Indication | Discovery agent | Investigative | [1] | ||
| Structure |
|
Download2D MOL |
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| Formula |
C23H28INO4
|
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| Canonical SMILES |
CCC[N+]1(CCC2=C(C1)C(=C(C3=C2C=CC4=CC(=C(C=C43)OC)O)OC)<br />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 | |||||
| Target(s) | Acetylcholinesterase | 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 | |||||
| Pathway Interaction Database | ATF-2 transcription factor network | ||||
| PathWhiz Pathway | Phospholipid Biosynthesis | ||||
| WikiPathways | Monoamine Transport | ||||
| Biogenic Amine Synthesis | |||||
| Acetylcholine Synthesis | |||||
| Integrated Pancreatic Cancer Pathway | |||||
| References | |||||
| REF 1 | J Nat Prod. 1998 Jan;61(1):46-50.Litebamine N-homologues: preparation and anti-acetylcholinesterase activity. | ||||
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