Drug Information
| Drug General Information | Top | |||
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| Drug ID |
D06IAQ
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| Former ID |
DAP000893
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| Drug Name |
Ambenonium
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| Synonyms |
Ambenonum; Ambenonium Base; Ambenonium kation; Mytelase (TN); (2-chlorophenyl)methyl-[2-[[2-[2-[(2-chlorophenyl)methyl-diethylazaniumyl]ethylamino]-2-oxoacetyl]amino]ethyl]-diethylazanium; 2,2'-[(1,2-dioxoethane-1,2-diyl)diimino]bis[n-(2-chlorobenzyl)-n,n-diethylethanaminium]
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| Drug Type |
Small molecular drug
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| Indication | Myasthenia gravis [ICD-11: 8C6Y; ICD-10: G70.0; ICD-9: 358] | Approved | [1] | |
| Therapeutic Class |
Antiarrhythmic Agents
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| Company |
Sanofi Aventis Us Llc
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| Structure |
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Download2D MOL |
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| Formula |
C28H42Cl2N4O2+2
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| Canonical SMILES |
CC[N+](CC)(CCNC(=O)C(=O)NCC[N+](CC)(CC)CC1=CC=CC=C1Cl)CC2=CC=CC=C2Cl
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| InChI |
1S/C28H40Cl2N4O2/c1-5-33(6-2,21-23-13-9-11-15-25(23)29)19-17-31-27(35)28(36)32-18-20-34(7-3,8-4)22-24-14-10-12-16-26(24)30/h9-16H,5-8,17-22H2,1-4H3/p+2
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| InChIKey |
OMHBPUNFVFNHJK-UHFFFAOYSA-P
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| CAS Number |
CAS 7648-98-8
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| PubChem Compound ID | ||||
| PubChem Substance ID |
9975, 5106491, 5792527, 8151446, 11113478, 26756578, 29221310, 46508143, 57321160, 76506773, 103107679, 103624065, 104111496, 104222117, 104299694, 117397200, 117465261, 124886912, 126407287, 134338170, 135027862, 136035395, 137005305, 160964456, 162656397, 175265408, 179225494, 196372339, 226628643, 241145075
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| ChEBI ID |
CHEBI:2627
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| SuperDrug ATC ID |
N07AA30
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| SuperDrug CAS ID |
cas=007648988
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| Target and Pathway | Top | |||
|---|---|---|---|---|
| Target(s) | Acetylcholinesterase (AChE) | Target Info | Inhibitor | [2] |
| 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 | FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (NDA) 010155. | |||
| REF 2 | Alpha6-containing nicotinic acetylcholine receptors dominate the nicotine control of dopamine neurotransmission in nucleus accumbens. Neuropsychopharmacology. 2008 Aug;33(9):2158-66. | |||
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