ChemicalBook--->CAS DataBase List--->158942-04-2

158942-04-2

158942-04-2 Structure

158942-04-2 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack 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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