| Identification | Back Directory |  [Name]
  AM 404 |  [CAS]
  183718-77-6 |  [Synonyms]
  AM 404 N-(4-HYDROXYPHENYL)-ARACHIDONAMIDE N-(4-HYDROXYPHENYL)ARACHIDONYLAMIDE N-(4-HYDROXYPHENYL) ARACHIDONOYLAMIDE ARACHIDONOYLAMIDE, N-(4-HYDROXYPHENYL) N-(4-HYDROXYPHENYL)-5Z,8Z,11Z,14Z-EICOSATETRENAMIDE N-(4-HYDROXYPHENYL)-5Z,8Z,11Z,14Z-EICOSATETRAENAMIDE (all-Z)-N-(4-Hydroxyphenyl)-5,8,11,14-eicosatetraenaMide (5Z,8Z,11Z,14Z)-N-(4-Hydroxyphenyl)-5,8,11,14-eicosatetraenaMide 5,8,11,14-Eicosatetraenamide, N-(4-hydroxyphenyl)-, (5Z,8Z,11Z,14Z)- |  [EINECS(EC#)]
  200-578-6 |  [Molecular Formula]
  C26H37NO2 |  [MDL Number]
  MFCD03095721 |  [MOL File]
  183718-77-6.mol |  [Molecular Weight]
  395.58 |  
 | Chemical Properties | Back Directory |  [Boiling point ]
  579.4±50.0 °C(Predicted) |  [density ]
  1.007±0.06 g/cm3(Predicted) |  [Fp ]
  14 °C |  [storage temp. ]
  -20°C |  [solubility ]
  ethanol: 24 mg/mL Photosensitive solution. |  [form ]
  solution |  [pka]
  10.11±0.26(Predicted) |  [color ]
  Colorless to light yellow |  
 | Hazard Information | Back Directory |  [Uses]
  It is a metabolite of the well-known analgesic Paracetamol.
ase (FAAH) in vivo. |  [Uses]
  Potentiates the activity of endogenous anandamide by blocking its re-uptake into presynaptic membranes. AM404 selectively inhibits the carrier-mediated transport of anandamide without affecting anandamide hydrolysis. |  [in vivo]
 
 AM404 (1-5 mg/kg, i.p.) exerts dose-dependent anxiolytic-like effects in the three models: elevated plus maze, defensive withdrawal and separation-induced ultrasonic vocalizations. | Animal Model: | Adult male Sprague-Dawley rats (250-300?g)[2] |  | Dosage: | 2.5-10?mg/kg |  | Administration: | Intraperitoneal (i.p.) |  | Result: | Caused a dose-dependent increase in anandamide levels in prefrontal cortex, hippocampus and thalamus.
 |  
  |  [storage]
  -20°C |  
  
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