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. | [storage]
-20°C |
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