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Medchemexpress LLC CB2R/FAAH modulator-3 | 2876918-67-9 | 99.7% | 341.49 g·mol⁻¹ | C22H31NO2 | 10 MG
SDP

Catalog No. 5000286409
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CB2R/FAAH modulator-3 is a small-molecule research compound that functions as a cannabinoid receptor 2 (CB2R) agonist and a fatty acid amide hydrolase (FAAH) inhibitor. Reported activity includes CB2R Ki = 20.1 nM, CB1R Ki = 67.6 nM, and FAAH IC50 = 3.4 μM. It is intended for preclinical studies of inflammatory signaling, neurodegeneration, cancer-related pathways, and infection-associated inflammatory responses.

  • Dual activity as CB2R agonist and FAAH inhibitor.
  • Reported high CB2R affinity (low nanomolar Ki).
  • Lower affinity for CB1R supporting receptor selectivity.
  • Applicable to studies of inflammation, neurodegeneration, and cancer biology.
  • High chemical purity suitable for research use.
  • Available in small-mass and solution formats for assay workflows.

Catalog No. 50-002-86409 Supplier Medchemexpress LLC Supplier No. HY15225410MG
May include imposed supplier surcharges.
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CB2R/FAAH modulator-3 is a small-molecule research compound that functions as a cannabinoid receptor 2 (CB2R) agonist and a fatty acid amide hydrolase (FAAH) inhibitor. Reported activity includes CB2R Ki = 20.1 nM, CB1R Ki = 67.6 nM, and FAAH IC50 = 3.4 μM. It is intended for preclinical studies of inflammatory signaling, neurodegeneration, cancer-related pathways, and infection-associated inflammatory responses.

  • Dual activity as CB2R agonist and FAAH inhibitor.
  • Reported high CB2R affinity (low nanomolar Ki).
  • Lower affinity for CB1R supporting receptor selectivity.
  • Applicable to studies of inflammation, neurodegeneration, and cancer biology.
  • High chemical purity suitable for research use.
  • Available in small-mass and solution formats for assay workflows.

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