| Name | palmitoyl ethanolamide |
|---|---|
| Synonyms |
Hexadecanamide ethanol (PEA)
PALMITAMIDE MEA PEA PALMIDROL Palmitoylethanolamide (PEA Micro) Mackpet DR 14V Palmidrol C-Palmitoylethanolamide Palmitoylethanolamide (PEA anule) Palmidrol -0 N-(2-Hydroxyethyl)hexadecanamide NeuReliv Liposomal Palmitoylethanolamide N-HEXADECANOYLETHANOLAMINE PuriActives PMEA N-(2-Hydroxyethyl)hexadecanamide, Palmidrol, PEA Hexadecamide ethanol Loramine P PEA anulSynonyms:Palmitoylethanolamide anul PALMITOYLETHANOLAMIDE ISO 9001:2015 REACH Cetylethanolamide Palmitoylethanolamide,PEA, Flake, anule powder, no any patent problems in pticle size Cetylamide ethanol PEA Micro Synonyms:Palmitoylethanolamide micro Palmitoylethanolamide(PEA) Top quality Palmitoylethanolamide(PEA ) -0 palmidrol Hexadecylamide ethanol EINECS 208-867-9 Palmitoylethanolamide(anul) Palmitic acid monoethanolamide PEA Synonyms:Palmitoylethanolamide MFCD00020562 Palmitoylethanolamide/Pea Powder Palmitoyl Ethanolamide PALMITOYLETHANOLAMIDE n-(2-hydroxyethyl)-hexadecanamid (Hydroxyethyl)palmitamide HexadecanaMide,N-(2-hydroxyethyl) Palmitoylethanolamide -0 Palmidrol AM 3112 N-(2-Hydroxyethyl)palmitic amide High quality Blue Lotus Leaf Extract 200:1 Impulsin N-(2-Hydroxyethyl)palmitamide Palmidrol (Palmitamide MEA) 2-(palmitoylamino)ethanol PEA Micro Palmitoylethanolamide - - Calbiochem PALMITOYLETHANOLIDE almitoylethanolamide PALMITOYLETHANOLAMIDE N-(2-HYDROXYETHYL)HEXADECANAMIDE Palmitoylethanolamide, 10 mM in DMSO PALMITYLETHANOLAMIDE N-palmitoylethanolamine 2-Palmitamidoethanol N-(2-Hydroxyethyl)hexadecanamide L-Histidine hydrochloride -2 N-(2-HYDROXYETHYL)HEXADECANAMIDE Palmitoylethanolamide micro (PEA Micro) PEA anul |
| Description | AM 3112 is an active endogenous compound which can used for preventing virus infection of the respiratory tract. |
|---|---|
| Related Catalog | |
| Target |
Human Endogenous Metabolite |
| In Vitro | AM 3112 (Impulsin) itself does not stimulate interferon production in mice treated per os or intravenously. But repeated application of this drug per os induces a macrophage activation, reflected by enhanced interferon production in vitro. When the interferon stimulation is delayed until 4 to 10 days after the first dose of AM 3112, interferon response to ds-RNA is slightly increased. After this phase of enhanced activity a decreased production of interferon is observed. AM 3112 is not significantly effective in protecting mice from lethal dose of EMC virus. Application of this drug has an inhibitory effect on the toxicity of ds-RNA. A possible explanation of the mechanism by which AM 3112 decreased the toxicity of virus in the organism is discussed[1]. |
| References |
| Density | 0.9±0.1 g/cm3 |
|---|---|
| Boiling Point | 461.5±28.0 °C at 760 mmHg |
| Melting Point | 99 °C |
| Molecular Formula | C18H37NO2 |
| Molecular Weight | 299.492 |
| Flash Point | 232.9±24.0 °C |
| Exact Mass | 299.282440 |
| PSA | 49.33000 |
| LogP | 5.82 |
| Vapour Pressure | 0.0±2.6 mmHg at 25°C |
| Index of Refraction | 1.463 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| RIDADR | NONH for all modes of transport |
| WGK Germany | 2 |
| HS Code | 2924199090 |
| Precursor 9 | |
|---|---|
| DownStream 6 | |
| HS Code | 2924199090 |
|---|---|
| Summary | 2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |