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EDROPHONIUM
SynDRA canonical compound SYN0003734 — structure-anchored drug synonym record
| Clinical phase | Launched |
|---|
| Approval status | Approved · OTC |
|---|
| Primary target(s) | ACHE |
|---|
| Mechanism of action | Acetylcholinesterase inhibitor |
|---|
| Indication | myasthenia gravis |
|---|
| Disease area | neurology/psychiatry |
|---|
All known targets
Mechanisms of action (all sources)
- Acetylcholinesterase inhibitor
- ACHE INHIBITOR
Bioactivity evidence (ChEMBL activities table — not curator-asserted)
- OPRM1
- ADORA1
- ADRA1A
- MAOA
- PDE3A
- PDE4A
- PGR
- POU2F1
- PTGS1
- SAMHD1
- SLC47A1
- SLC47A2
- SLC6A2
- SLC6A3
- SLC6A4
- SLCO1B1
- SLCO1B3
- SMN1
- TBXA2R
- HTR2B
- HTR1A
- HRH3
- CYP2C19
- ADRA2A
- APEX1
- AR
- BLM
- CHRM1
- CHRM2
- CYP1A2
- CYP2C9
- HDAC6
- CYP2D6
- CYP3A4
- DRD1
- DRD3
- EHMT2
- ESR1
- F2
- TSHR
Screening evidence (raw PubChem HTS — uncurated, known false-positive rate)
Drug classes
- Cholinesterase Inhibitors
- Antidotes
- Cholinergic Agents
- Enzyme Inhibitors
- Neurotransmitter Agents
- Protective Agents
- Cholinesterase Inhibitor
ATC classes
- V04C · OTHER DIAGNOSTIC AGENTS
Cross-references
Synonyms
- EDROPHONIUM CHLORIDE
- EDROPHONIUM CHLORIDE PRESERVATIVE FREE
- ENLON
- ENLON-PLUS
- REVERSOL
- TENSILON
- TENSILON PRESERVATIVE FREE
- edrophonium chloride
- Edrophonium cation
- Edrophonium ion
- Enlon-plus
- EDR
- Edrophonum
- Edroponium
- Reversol
- Tensilon
- EDROPHONIUM ION
- Edrophone Chloride
- Enlon (TN)
- Reversol (TN)
- Tensilon (TN)
- Ethyl-(3-hydroxyphenyl)-dimethylazanium
- Ethyl-(3-hydroxy-phenyl)-dimethyl-ammonium
- N-ethyl-3-hydroxy-N,N-dimethylanilinium
- N-ethyl-3-hydroxy-N,N-dimethylbenzenaminium
- (3-hydroxyphenyl)dimethylethylammonium
- 3-hydroxy-N,N-dimethyl-N-ethylanilinium
- ethyl-(3-hydroxyphenyl)-dimethylazanium
- Benzenaminium, N-ethyl-3-hydroxy-N,N-dimethyl-
- CHEBI:251408
- RefChem:63136
- DTXCID2026943
- Edrofonio cloruro [DCIT]
- Ammonium, ethyl(m-hydroxyphenyl)dimethyl-(8CI)
- NCGC00015409-02
- CAS-116-38-1
- UNII-70FP3JLY7N
- Spectrum_000442
Reported adverse events
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