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$0.00 Biological Activity
Detomidine is a sedative with analgesic properties. α2-adrenergic agonists produce dose-dependent sedative and analgesic effects, mediatated by activation of α2 catecholamine receptors, thus inducing a negative feedback response, reducing production of excitatory neurotransmitters.
Targets
| Adrenergic Receptor | ||||
| In vitro | DMSO | 41 mg/mL (184.09 mM) | |
| Water | 41 mg/mL (184.09 mM) | ||
| Ethanol | 41 mg/mL (184.09 mM) | ||
|
* <1 mg/ml means slightly soluble or insoluble. * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. |
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| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 0.1 mM | 44.9 mL | 224.52 mL | 449.03 mL |
| 0.5 mM | 8.98 mL | 44.9 mL | 89.81 mL |
| 1 mM | 4.49 mL | 22.45 mL | 44.9 mL |
| 5 mM | 0.9 mL | 4.49 mL | 8.98 mL |
*The above data is based on the productmolecular weight 222.7 . Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
| Catalog Num | A10298 |
|---|---|
| Actions | Agonist |
| CAS No. | 90038-01-0 |
| Formula | C12H14N2.HCl |
| M. Wt | 222.7 |
| Purity | >98% |
| SMILES | CC1=C(C(=CC=C1)CC2=CN=CN2)C.Cl |
| Storage | Store lyophilized at -20ºC, keep desiccated. |
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