AM6701
AM6701 is a potent dual FAAH/MAGL inhibitor (IC50 = 1.2 nM) that provides neuroprotection by elevating endocannabinoid tone. Its mechanism involves suppressing calpain-mediated excitotoxicity, supporting its research use in models of neurological injury and neurodegeneration both in vitro and in vivo.
Product Specifications
CAS Number
1010096-65-7
Product Name Alternative
AM6701, AM-6701, AM 6701, CX 5011., CX-5011, FAAH/MAGL-IN-5
Field of Research
Metabolism Research, Neuroscience
Purity
99.25% (May vary between batches)
Solubility
10% DMSO+40% PEG300+5% Tween-80+45% Saline:3.3 mg/mL (10.74 mM) ; DMSO:80 mg/mL (260.28 mM)
Smiles
CN (C) C (=O) n1nnc (Cc2ccc (cc2) -c2ccccc2) n1
Molecular Formula
C17H17N5O
Molecular Weight
307.36
Storage Conditions
-20°C
Notes
For research use only.
Available Sizes
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GABPB1, CT (GABPB1, E4TF1B, GABPB, GABPB2, GA-binding protein subunit beta-1, GABP subunit beta-2, Nuclear respiratory factor 2, Transcription factor E4TF1-47, Transcription factor E4TF1-53) (PE)
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GABPB1, CT (GABPB1, E4TF1B, GABPB, GABPB2, GA-binding protein subunit beta-1, GABP subunit beta-2, Nuclear respiratory factor 2, Transcription factor E4TF1-47, Transcription factor E4TF1-53) (PE)
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