FAAH
- Label
- FAAH (literal)
- Membro di
- Keywords of "N-acyl-dopamines: novel synthetic CB1 cannabinoid-receptor ligands and inhibitors of anandamide inactivation with cannabimimetic activity in vitro and in vivo" (Insieme di parole chiave)
- Parole chiave di "The First Dual ChE/FAAH Inhibitors: New Perspectives for Alzheimer's Disease?" (Insieme di parole chiave)
- Parole chiave di "Molecular targets for cannabidiol and its synthetic analogues: effect on vanilloid VR1 receptors and on the cellular uptake and enzymatic hydrolysis of anandamide" (Insieme di parole chiave)
- Keywords of "Biosynthesis and inactivation of the endocannabinoid 2-arachidonoylglycerol in circulating and tumoral macrophages." (Insieme di parole chiave)
- Keywords of "Effects of a short-term exposure to alcohol in rats on FAAH enzyme and CB1 receptor in different brain areas" (Insieme di parole chiave)
- Keywords of "Tetrahydro-beta-carboline derivatives targeting fatty acid amide hydrolase (FAAH) and transient receptor potential (TRP) channels. ." (Insieme di parole chiave)
- Parole chiave di "Innate difference in the endocannabinoid signaling and its modulation by alcohol consumption in alcohol-preferring sP rats" (Insieme di parole chiave)
- Keywords of "Latest advances in the discovery of fatty acid amide hydrolase inhibitors." (Insieme di parole chiave)
- Parole chiave di "Membrane lipids are key-modulators of the endocannabinoid-hydrolase FAAH" (Insieme di parole chiave)
- Keywords of "Further evidence for the existence of a specific process for the membrane transport of anandamide." (Insieme di parole chiave)
- Parole chiave di "Novel selective and metabolically stable inhibitors of anandamide cellular uptake." (Insieme di parole chiave)
- Parole chiave di "Anxiolytic effects in mice of a dual blocker of fatty acid amide hydrolase and transient receptor potential vanilloid type-1 channels" (Insieme di parole chiave)
- Keywords of "Analgesic actions of N-arachidonoyl-serotonin, a fatty acid amide hydrolase inhibitor with antagonistic activity at vanilloid TRPV1 receptors" (Insieme di parole chiave)
- Value
- FAAH (literal)
Incoming links:
- Ha membro
- Keywords of "Effects of a short-term exposure to alcohol in rats on FAAH enzyme and CB1 receptor in different brain areas" (Insieme di parole chiave)
- Parole chiave di "Anxiolytic effects in mice of a dual blocker of fatty acid amide hydrolase and transient receptor potential vanilloid type-1 channels" (Insieme di parole chiave)
- Keywords of "N-acyl-dopamines: novel synthetic CB1 cannabinoid-receptor ligands and inhibitors of anandamide inactivation with cannabimimetic activity in vitro and in vivo" (Insieme di parole chiave)
- Keywords of "Latest advances in the discovery of fatty acid amide hydrolase inhibitors." (Insieme di parole chiave)
- Keywords of "Analgesic actions of N-arachidonoyl-serotonin, a fatty acid amide hydrolase inhibitor with antagonistic activity at vanilloid TRPV1 receptors" (Insieme di parole chiave)
- Keywords of "Tetrahydro-beta-carboline derivatives targeting fatty acid amide hydrolase (FAAH) and transient receptor potential (TRP) channels. ." (Insieme di parole chiave)
- Parole chiave di "The First Dual ChE/FAAH Inhibitors: New Perspectives for Alzheimer's Disease?" (Insieme di parole chiave)
- Parole chiave di "Membrane lipids are key-modulators of the endocannabinoid-hydrolase FAAH" (Insieme di parole chiave)
- Keywords of "Further evidence for the existence of a specific process for the membrane transport of anandamide." (Insieme di parole chiave)
- Parole chiave di "Novel selective and metabolically stable inhibitors of anandamide cellular uptake." (Insieme di parole chiave)
- Parole chiave di "Innate difference in the endocannabinoid signaling and its modulation by alcohol consumption in alcohol-preferring sP rats" (Insieme di parole chiave)
- Keywords of "Biosynthesis and inactivation of the endocannabinoid 2-arachidonoylglycerol in circulating and tumoral macrophages." (Insieme di parole chiave)
- Parole chiave di "Molecular targets for cannabidiol and its synthetic analogues: effect on vanilloid VR1 receptors and on the cellular uptake and enzymatic hydrolysis of anandamide" (Insieme di parole chiave)