Identification | Back Directory | [Name]
5-METHYL-1-(3-PYRIDYLCARBAMOYL)-1,2,3,5-TETRAHYDROPYRROLO [2,3-F]INDOLE | [CAS]
158942-04-2 | [Synonyms]
SB 206553 SB 206553 HCL SB 206553 HYDROCHLORIDE SB-206553 hydrochloride hydrate SB-206553 hydrate hydrochloride 1-amino-2-bromo-4-(2-methylanilino)anthracene-9,10-dione 5-METHYL-1-(3-PYRIDYLCARBAMOYL)-1,2,3,5-TETRAHYDROPYRROLO [2,3-F]INDOLE 5-Methyl-N-(pyridin-3-yl)-2,3-dihydropyrrolo[2,3-f]indole-1(5H)-carboxamide 5-METHYL-3,5-DIHYDRO-2H-PYRROLO[2,3-F]INDOLE-1-CARBOXYLIC ACID PYRIDIN-3-YLAMIDE Benzo[1,2-b:4,5-b']dipyrrole-1(2H)-carboxamide, 3,5-dihydro-5-methyl-N-3-pyridinyl- 5-methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indole hydrochloride 5-Methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indole hydrochloride hydrate 3,5-DIHYDRO-5-METHYL-N-3-PYRIDINYLBENZO[1,2-B:4,5-B']DIPYRROLE-1(2H)-CARBOXAMIDE HYDROCHLORIDE N-3-PYRIDINYL-3,5-DIHYDRO-5-METHYL-BENZO[1,2-B:4,5-B']DIPYRROLE-1(2H)-CARBOXAMIDE HYDROCHLORIDE N-3-Pyridinyl-3,5-dihydro-5-methylbenzo(1,2-b:4,5-b′)dipyrrole-1(2H)carboxamide hydrochloride hydrate N-3-Pyridinyl-3,5-dihydro-5-methylbenzo(1,2-b:4,5-bμ)dipyrrole-1(2H)carboxamide hydrate hydrochloride, 5-Methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indole hydrate hydrochloride | [Molecular Formula]
C17H16N4O | [MDL Number]
MFCD00928314 | [MOL File]
158942-04-2.mol | [Molecular Weight]
292.34 |
Chemical Properties | Back Directory | [Boiling point ]
575.4±50.0 °C(Predicted) | [density ]
1.33±0.1 g/cm3(Predicted) | [storage temp. ]
Desiccate at RT | [solubility ]
H2O: 30 mg/mL | [form ]
solid | [pka]
13.50±0.20(Predicted) | [color ]
brown |
Hazard Information | Back Directory | [Uses]
SB 206553 Hydrochloride is a 5-HT2 antagonist. | [Definition]
ChEBI: SB 206553 is a pyrroloindole. | [Biological Activity]
Potent and selective 5-HT 2B /5-HT 2C receptor antagonist (rat 5-HT 2B pA 2 = 8.89, human 5-HT 2C pK i = 7.92). Displays > 80-fold selectivity over all other 5-HT receptor subtypes and a variety of other receptors (pK i < 6). Centrally active following oral administration in vivo . |
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