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Physostigmine is an alkaloid extracted from the poison bean (Physostigma venenosum) and acts as a reversible acetylcholinesterase (AChE) inhibitor. Physostigmine inhibits the action of acetylcholinesterase, increasing acetylcholine levels, and thus serves as an antidote for anticholinergic poisoning. Physostigmine crosses the blood-brain barrier and stimulates central cholinergic neurotransmission. Physostigmine can reverse memory deficits in transgenic mice with Alzheimer's disease.

| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 1 mg | $189 | - | In Stock | |
| 5 mg | $475 | - | In Stock | |
| 10 mg | $682 | - | In Stock | |
| 25 mg | $987 | - | In Stock | |
| 50 mg | $1,380 | - | In Stock |
| Description | Physostigmine is an alkaloid extracted from the poison bean (Physostigma venenosum) and acts as a reversible acetylcholinesterase (AChE) inhibitor. Physostigmine inhibits the action of acetylcholinesterase, increasing acetylcholine levels, and thus serves as an antidote for anticholinergic poisoning. Physostigmine crosses the blood-brain barrier and stimulates central cholinergic neurotransmission. Physostigmine can reverse memory deficits in transgenic mice with Alzheimer's disease. |
| In vitro | Methods: Tissue homogenates were prepared from the CA3-CA1 region of the hippocampus. After perfusion with 10 μM Physostigmine for 20 minutes, acetylcholinesterase (AChE) activity was measured using a colorimetric assay immediately after perfusion, 20 minutes after elution, and 1 hour after elution. Results: AChE activity increased after 20 min of Physostigmine perfusion, returned to baseline after 20 min of elution, and showed a compensatory increase after 1 h of elution. [1] Methods: Primary rat cortical neurons were treated with Physostigmine (0.01, 0.1, 1.0, 10, 100 nM) for 24 h. Live-cell imaging (1 frame every 2 seconds for a total of 3 minutes) was performed to generate a kymograph, which was analyzed using KymoAnalyzer. Results: None of the Physostigmine concentrations had a significant effect on axonal transport velocity (anterior direction); conversely, the highest concentration (100 nM) significantly increased retrograde transport velocity.[2] |
| In vivo | Methods: To investigate the effects of Physostigmine, adult male C57BL/6J mice were administered Physostigmine (0.25 mg/kg) via intraperitoneal injection. Twenty minutes after the initial injection, ketamine (5 mg/kg) was administered intraperitoneally. The forced swim test was conducted 50 minutes later, and the immobility time within the first 4 minutes was recorded. Results: Physostigmine significantly increased the immobility time; ketamine significantly reduced the increase in immobility time induced by Physostigmine, indicating that Physostigmine impairs neurotransmission. [1] |
| Synonyms | Eserine |
| Molecular Weight | 275.35 |
| Formula | C15H21N3O2 |
| Cas No. | 57-47-6 |
| Smiles | C[C@]12C=3C(N(C)[C@]1(N(C)CC2)[H])=CC=C(OC(NC)=O)C3 |
| Relative Density. | 1.166g/cm3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 40 mg/mL (145.27 mM), Sonication is recommended. H2O: Insoluble | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density. | ||||||||||||||||||||||||||||||||||||
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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