N-(4-Hydroxyphenyl)-arachidonylamide

• Catalog No.: H1911
• CAS Number: 183718-77-6
• M. F.: C26H37NO2
• M. W.: 395.57748
• Purity: ≥98%

SYNONYMS

• IUPAC name: N-(4-hydroxyphenyl)icosa-5,8,11,14-tetraenamide
• IUPAC Traditional name: N-(4-hydroxyphenyl)icosa-5,8,11,14-tetraenamide
• Synonyms: AM404

DATABASE IDS

• MDL Number: MFCD03095721
• CAS Number: 183718-77-6
• PubChem SID: 24895490

PROPERTIES

• Empirical Formula (Hill Notation): C26H37NO2
• Purity: ≥98%
• Shipped in: wet ice
• Gene Information: human ... CNR1(1268), CNR2(1269)mouse ... Cnr2(12802)rat ... Cnr1(25248), Faah(29347), Trpv1(83810)
• Apperance: ethanol solution
• Flash Point: 14 °C
• Flash Point: 57.2 °F
• GHS Signal Word: Danger
• GHS Hazard statements: H225
• European Hazard Symbols: Flammable (F)
• Personal Protective Equipment: Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• GHS Precautionary statements: P210
• RID/ADR: UN 1170 3/PG 2
• Risk Statements: 11
• Safety Statements: 16
• Storage Temperature: -20°C
• Hazard Class: 3
• UN Number: 1170
• Packing Group: 2
• German water hazard class: 2

DETAILS

Description (English)

Other Notes
To change the solvent, simply evaporate the ethanol under a gentle stream of nitrogen and immediately add the solvent of choice.
Application
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.

Description (简体中文)

Other Notes
To change the solvent, simply evaporate the ethanol under a gentle stream of nitrogen and immediately add the solvent of choice.
Application
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.