| Name | omdm-1 |
|---|---|
| Synonyms |
(9Z)-N-[(2S)-1-Hydroxy-3-(4-hydroxyphenyl)-2-propanyl]-9-octadecenamide
9-Octadecenamide, N-[(1S)-2-hydroxy-1-[(4-hydroxyphenyl)methyl]ethyl]-, (9Z)- |
| Description | OMDM-1 is a potent, selective and metabolically stable inhibitor of anandamide cellular uptake (ACU), with a Ki of 2.4 μM[1]. |
|---|---|
| Related Catalog | |
| Target |
Ki: 2.4 μM (anandamide cellular uptake)[1] |
| In Vitro | OMDM-1 shows poor affinity for either CB1 (Ki=12.1 μM) or CB2 (Ki>10 μM) receptors in rat brain and spleen membranes, respectively; OMDM-1 has almost no activity at vanilloid receptors in the intracellular calcium assay carried out with intact cells over-expressing the human VR1 (EC50≥10 μM), and no activity as inhibitors of FAAH in N18TG2 cell membranes (Ki>50 μM)[1]. |
| References |
| Density | 1.0±0.1 g/cm3 |
|---|---|
| Boiling Point | 625.8±55.0 °C at 760 mmHg |
| Molecular Formula | C27H45NO3 |
| Molecular Weight | 431.651 |
| Flash Point | 332.3±31.5 °C |
| Exact Mass | 431.339935 |
| PSA | 69.56000 |
| LogP | 7.76 |
| Vapour Pressure | 0.0±1.9 mmHg at 25°C |
| Index of Refraction | 1.518 |
| HS Code | 2924299090 |
|---|
| HS Code | 2924299090 |
|---|---|
| Summary | 2924299090. other cyclic amides (including cyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0% |