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SB 243213 dihydrochloride manufacturers
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| | SB 243213 dihydrochloride Basic information |
| Product Name: | SB 243213 dihydrochloride | | Synonyms: | 5-Methyl-N-{6-[(2-methylpyridin-3-yl)oxy]pyridin-3-yl}-6-(trifluoromethyl)-2,3-dihydro-1H-indole-1-carboxamide dihydrochloride | | CAS: | 1780372-25-9 | | MF: | C22H20ClF3N4O2 | | MW: | 464.87 | | EINECS: | | | Product Categories: | | | Mol File: | 1780372-25-9.mol |  |
| | SB 243213 dihydrochloride Chemical Properties |
| solubility | DMSO: 50mM; Ethanol: 100mM | | form | A solid | | color | Light yellow to yellow |
| | SB 243213 dihydrochloride Usage And Synthesis |
| Uses | SB 243213 Dihydrochloride is a 5-HT2c receptor antagonist. | | in vivo | SB 243213 dihydrochloride (0.1-10 mg/kg; p.o.; 1 h pre-test) dose-dependently and significantly increases the amount of time rats spent in social interaction over 15 min under brightly lit conditions and in an unfamiliar test box[1].
SB 243213 dihydrochloride (0.3 mg/kg; p.o.; 1 h pre-test) significantly increases time spent in social interaction[1].
| Animal Model: | Male Sprague-Dawley experimentally naive rats (220-300 g)[1] | | Dosage: | 0.1, 0.3, 1, 3, 10 mg/kg | | Administration: | p.o.; 1 hour pre-test | | Result: | Dose-dependently and significantly increased the amount of time rats spent in social interaction over 15 min under brightly lit conditions and in an unfamiliar test box.
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| | IC 50 | Human 5-HT2C Receptor: 9.37 (pKi); human 5-HT1A Receptor: <5.3 (pKi); human 5-HT1B Receptor: 5.5 (pKi); human 5-HT1D Receptor: 6.32 (pKi); human 5-HT1E Receptor: <5.4 (pKi); human 5-HT1F Receptor: 5.35 (pKi); Human 5-HT2A Receptor: 7.01 (pKi); human 5-HT2B Receptor: 7.2 (pKi); Human 5-HT6 Receptor: 6.5 (pKi); Human 5-HT7 Receptor: 5.64 (pKi) |
| | SB 243213 dihydrochloride Preparation Products And Raw materials |
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