AM1172
AM1172 Basic information
- Product Name:
- AM1172
- Synonyms:
-
- N-5Z,8Z,11Z,14Z-EICOSATETRAENYL-4-HYDROXY-BENZAMIDE
- 4-hydroxy-N-[(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenyl]benzamide
- AM1172
- N-(5Z,8Z,11Z,14Z)-5,8,11,14-eicosatetraen-1-yl-4-hydroxybenzamide
- Benzamide, N-(5Z,8Z,11Z,14Z)-5,8,11,14-eicosatetraen-1-yl-4-hydroxy-
- CAS:
- 251908-92-6
- MF:
- C27H39NO2
- MW:
- 409.6
- Mol File:
- 251908-92-6.mol
AM1172 Chemical Properties
- Boiling point:
- 590.8±50.0 °C(Predicted)
- Density
- 0.983±0.06 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- Soluble in ethanol
- form
- solution in ethanol
- pka
- 8.53±0.26(Predicted)
AM1172 Usage And Synthesis
Uses
AM 1172 is a potent and selective inhibitor of anandamide uptake and FAAH.
Biological Activity
Metabolically stable anandamide uptake inhibitor (IC 50 = 2.1 - 2.5 μ M) and fatty acid amide hydrolase (FAAH) inhibitor (K i = 3.18 μ M). Inhibits N -arachidonylethanolamine (AEA) accumulation (IC 50 = 24 μ M) and hydrolysis (K i = 3 μ M), and inhibits N -palmitoylethanolamine (PEA) hydrolysis (IC 50 = 36 μ M) in cerebellar granule neurons. Also acts as a non-selective cannabinoid receptor partial agonist (EC 50 values are 189 and 271 nM at CB 2 and CB 1 receptors respectively).
References
1. fegley d, kathuria s, mercier r, et al. anandamide transport is independent of fatty-acid amide hydrolase activity and is blocked by the hydrolysis-resistant inhibitor am1172. proceedings of the national academy of sciences of the united states of america. 2004;101(23):8756-8761.
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