N-Arachidonoyl Dopamine (NADA) Research Dashboard
Double-blind human trials
Clinical human trials
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CannaKeys has 35 studies associated with N-Arachidonoyl Dopamine (NADA).
Here is a small sampling of N-Arachidonoyl Dopamine (NADA) studies by title:
- Influence of N-Arachidonoyl Dopamine and N-Docosahexaenoyl Dopamine on the Expression of Neurotrophic Factors in Neuronal Differentiated Cultures of Human Induced Pluripotent Stem Cells under Conditions of Oxidative Stress
- Neuroprotective and neurotoxic effects of endocannabinoid-like compounds, N-arachidonoyl dopamine and N-docosahexaenoyl dopamine in differentiated cultures of induced pluripotent stem cells derived from patients with Parkinson's disease
- N-arachidonoyl dopamine inhibits epithelial-mesenchymal transition of breast cancer cells through ERK signaling and decreasing the cellular cholesterol
- Polypharmacological Approaches for CNS Diseases: Focus on Endocannabinoid Degradation Inhibition
- Early-life N-arachidonoyl-dopamine exposure increases antioxidant capacity of the brain tissues and reduces functional deficits after neonatal hypoxia in rats
Components of the N-Arachidonoyl Dopamine (NADA) Research Dashboard
- Top medical conditions associated with N-Arachidonoyl Dopamine (NADA)
- Proven effects in clinical trials for N-Arachidonoyl Dopamine (NADA)
- Receptors associated with N-Arachidonoyl Dopamine (NADA)
- Individual study details for N-Arachidonoyl Dopamine (NADA)
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Overview - N-Arachidonoyl Dopamine (NADA)
Description of N-Arachidonoyl Dopamine (NADA)
N-acyldopamines are a group of endocannabinoids of which N-arachidonoyl dopamine (NADA) is one of its most prominent and most studied members.
NADA is present in very low concentrations in various portions of the brain such as the striatum, hippocampus, cerebellum, thalamus, midbrain, and dorsal root ganglia for example.
Additionally a novel class of synthetic anandamide (AEA) analogues were described by a group of Italian researchers (T. Bisogno et al., 2000).
Arachidonoyl dopamine, N-Arachidonyldopamine, NADA dopamine and others.
IUPAC Name: (5Z,8Z,11Z,14Z)-N-[2-(3,4-dihydroxyphenyl)ethyl]icosa-5,8,11,14-tetraenamide
Molecular Formula: C28H41NO3
N-Arachidonoyl Dopamine (NADA) Properties and Effects
- In vivo effects of NADA included hypothermia, hypo-locomotion, catalepsy and analgesia in the test animals.
- Inhibitor of human breast MCF-7 cancer cells.
- Induce anti-oxidative properties.
- Modulates immune cells
- Mediates vasorelaxation.
- Inhibit aggregation of human platelets.
N-Arachidonoyl Dopamine (NADA) Receptor Binding
Endocannabinoid system (ECS) and NADA:
- CB1 agonist with a Ki ~0.25nM (T. Bisogno et al., 2000)
- CB2 agonist with a Ki ~12nM (T. Bisogno et al., 2000)
- FAAH inhibitor (Urszula Grabiec et al. 2017)
- MAGL inhibitor (E Björklund et al. 2010)
Endocannabinoidome (eCBome) and NADA:
- TRPV1 agonist (Urszula Grabiec et al. 2017)
- TRPM8 antagonist (Luciano De Petrocellis et al. 2007)
- Full/strong agonist Ki ~1-9nM
- Moderate agonist Ki ~10-99nM
- Weak agonist Ki ~100-999nM
- Very weak agonist Ki ~1,000-up nM
(The reader is reminded that a smaller Ki is associated with the strongest effects.)
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Information on this site is based on scientific studies (human, animal, or in vitro), clinical experience, or traditional usage as cited in each article. The results reported may not necessarily occur in all individuals. For many of the conditions discussed, treatment with prescription or over-the-counter medication is also available. Consult your physician, nutritionally oriented health care practitioner, and/or pharmacist for any health problem and before using any supplements or before making any changes in prescribed medications.