1. GPCR/G Protein
    Neuronal Signaling
    Metabolic Enzyme/Protease
  2. Cannabinoid Receptor
    Endogenous Metabolite
  3. Anandamide

Anandamide (Synonyms: (5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide)

Cat. No.: HY-10863 Purity: >99.0%
Handling Instructions

Anandamide is an immune modulator in the central nervous system acts via not only cannabinoid receptors (CB1 and CB2) but also other targets (e.g., GPR18/GPR55).

For research use only. We do not sell to patients.

Anandamide Chemical Structure

Anandamide Chemical Structure

CAS No. : 94421-68-8

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5 mg (144 mM * 100  μL in Ethanol) USD 95 Ask For Quote & Lead Time
10 mg (144 mM * 200  μL in Ethanol) USD 160 Ask For Quote & Lead Time

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Anandamide is an immune modulator in the central nervous system acts via not only cannabinoid receptors (CB1 and CB2) but also other targets (e.g., GPR18/GPR55).

IC50 & Target[1]







Human Endogenous Metabolite


In Vitro

Anandamide, acting via CB2 receptors, alleviates lipopolysaccharide (LPS)-induced neuroinflammation in rat primary microglial cultures. The endocannabinoid system modulates both neuronal and immune functions through two protein-coupled cannabinoid receptors (CB1 and CB2), although endocannabinoids, especially Anandamide (AEA), can activate numerous other receptors like PPARS, TRPV1, and GPR18/GPR55[1].

In Vivo

Anandamide is an endocannabinoid binding both CB1R and CB2R. To evaluate the impact of CBR activation on whole-body glucose homeostasis, glucose tolerance is assessed after a single intraperitoneal Anandamide injection (10 mg/kg). The increase in glycemia in response to glucose ingestion is considerably smaller in mice treated with Anandamide compared with control, and this is associated with an improvement of glucose tolerance as illustrated by the AUC0-2h calculations[2].

Molecular Weight









Room temperature in continental US; may vary elsewhere.


Solution, -20°C, 2 years

Solvent & Solubility
In Vitro: 

Ethanol : ≥ 10 mg/mL (28.77 mM)

*"≥" means soluble, but saturation unknown.

Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.8774 mL 14.3872 mL 28.7745 mL
5 mM 0.5755 mL 2.8774 mL 5.7549 mL
10 mM 0.2877 mL 1.4387 mL 2.8774 mL
*Please refer to the solubility information to select the appropriate solvent.
Animal Administration

Eleven-week-old C57BL/6J male mice and global CB1R-/- mice are housed individually on a 12/12-h light/dark schedule at 22-23°C with ad libitum access to water and food. A group of mice is subject to a high-fat diet (30% lard). After 16 weeks of diet, animals with a weight gain less than +10 g compared with controls are excluded from the study. Diet-induced obesity (DIO) mice (39.1±1.1 vs. 27.3±0.9 g, DIO vs. control) are glucose intolerant and insulin resistant. On the day of each experiment, food is removed from the cages for 6 h (from 8:00 A.M. to 2:00 P.M.). Anandamide is administered intraperitoneally at 10 mg/kg. In control experiments, animals are injected with vehicle (4% DMSO/1% Tween 80)[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.


Purity: >99.0%

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Anandamide(5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamideCannabinoid ReceptorGPR55Endogenous MetaboliteG protein-coupled receptor 55Inhibitorinhibitorinhibit

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