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AM6701 is an effective dual inhibitor of FAAH (fatty acid amide hydrolase) and MAGL (monoacylglycerol lipase), with an IC50 of 1.2 nM. It exhibits neuroprotective effects by modulating endogenous cannabinoids and inhibiting calpain-mediated excitotoxic brain injury.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $81 | - | In Stock | |
| 2 mg | $113 | - | In Stock | |
| 5 mg | $179 | - | In Stock | |
| 10 mg | $288 | - | In Stock | |
| 25 mg | $579 | - | In Stock | |
| 50 mg | $928 | - | In Stock | |
| 100 mg | $1,250 | - | In Stock | |
| 200 mg | $1,680 | - | In Stock |
| Description | AM6701 is an effective dual inhibitor of FAAH (fatty acid amide hydrolase) and MAGL (monoacylglycerol lipase), with an IC50 of 1.2 nM. It exhibits neuroprotective effects by modulating endogenous cannabinoids and inhibiting calpain-mediated excitotoxic brain injury. |
| Targets&IC50 | FAAH/MAGL:1.2 nM |
| Synonyms | FAAH/MAGL-IN-5 |
| Molecular Weight | 307.36 |
| Formula | C17H17N5O |
| Cas No. | 1010096-65-7 |
| Smiles | CN(C)C(=O)n1nnc(Cc2ccc(cc2)-c2ccccc2)n1 |
| Color | White |
| Appearance | Solid |
| Storage | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (260.28 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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