Drug Information
Drug General Information | Top | |||
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Drug ID |
D0O1JC
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Former ID |
DNC012354
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Drug Name |
2-Hex-5-enyl-5-nonyl-pyrrolidine
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Synonyms |
2-hex-5-enyl-5-nonylpyrrolidine; CHEMBL417618; 100594-88-5; 2-hex-5-enyl-5-nonyl-pyrrolidine; Pyrrolidine, 2-(5-hexenyl)-5-nonyl-; AC1L481F; 2-(5-hexenyl)-5-nonylpyrrolidine; BDBM50284429
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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 |
C19H37N
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Canonical SMILES |
CCCCCCCCCC1CCC(N1)CCCCC=C
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InChI |
1S/C19H37N/c1-3-5-7-9-10-11-13-15-19-17-16-18(20-19)14-12-8-6-4-2/h4,18-20H,2-3,5-17H2,1H3
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InChIKey |
VJYHAIYEEJOCLT-UHFFFAOYSA-N
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CAS Number |
CAS 100594-88-5
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PubChem Compound ID |
Target and Pathway | Top | |||
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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 | |||
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REF 1 | Acetylcholinesterase inhibition by alkaloids of the ant's venom Monomorium minutum, Bioorg. Med. Chem. Lett. 5(11):1131-1132 (1995). |
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