Antibodies
SL327 is a selective inhibitor for MEK1/2 with IC50 of 0.18 μM/ 0.22 μM, no activity towards Erk1, MKK3, MKK4, c-JUN, PKC, PKA, or CamKII;capable of transport through the blood-brain barrier.
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| Description | SL327 is a selective inhibitor for MEK1/2 with IC50 of 0.18 μM/ 0.22 μM, no activity towards Erk1, MKK3, MKK4, c-JUN, PKC, PKA, or CamKII;capable of transport through the blood-brain barrier. | |||||
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| Targets | MEK1 | MEK2 | ||||
| IC50 | 0.18 μM | 0.22 μM [1] | ||||
| In vitro | SL327 is a water soluble, structural homologue of the specific MKK1/2 inhibitor U0126 with IC50 of 0.18 μM and 0.22 μM for MEK1 and MEK2 respectively. SL327 has no effect on a variety of other kinases, including PKA, PKC, or CamKII. [1] | |||||
| In vivo | SL327 (50 mg/Kg) crosses the blood-brain barrierand and blocks fear conditioning by inhibiting MAPK/ERK phosphorylation. [1] SL327 (30 mg/Kg) significantly impairs spatial learning in mice. [2] SL327 (50 mg/Kg) blocks cocaine-induced properties. [3] | |||||
| Features | ||||||
| Animal Models | Fear conditioning experiments in male Spague-Dawley rats. |
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| Dosages | 10-100 mg/Kg |
| Administration | i.p. |
| Molecular Weight (MW) | 335.35 |
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| Formula | C16H12F3N3S |
| CAS No. | 305350-87-2 |
| Storage | 3 years -20℃Powder |
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| 6 months-80℃in DMSO | |
| Syonnyms | N/A |
| Solubility (25°C) * | In vitro | DMSO | 4 mg/mL (11 mM) |
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| Water | <1 mg/mL (<1 mM) | ||
| Ethanol | 7 mg/mL (20 mM) | ||
| * <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck 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. | |||
| Chemical Name | (Z)-3-amino-3-(4-aminophenylthio)-2-(2-(trifluoromethyl)phenyl)acrylonitrile |
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| Stock Solution (1ml DMSO) | 1mM | 10mM | 20mM | 30mM |
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| Mass(mg) | 0.33535 | 3.3535 | - | - |