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| | 5-Methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo [2,3-f]indole Basic information |
| Product Name: | 5-Methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo [2,3-f]indole | | Synonyms: | 3,5-DIHYDRO-5-METHYL-N-3-PYRIDINYLBENZO[1,2-B:4,5-B']DIPYRROLE-1(2H)-CARBOXAMIDE HYDROCHLORIDE;SB 206553;SB 206553 HYDROCHLORIDE;N-3-PYRIDINYL-3,5-DIHYDRO-5-METHYL-BENZO[1,2-B:4,5-B']DIPYRROLE-1(2H)-CARBOXAMIDE HYDROCHLORIDE;SB 206553 HCL;5-METHYL-3,5-DIHYDRO-2H-PYRROLO[2,3-F]INDOLE-1-CARBOXYLIC ACID PYRIDIN-3-YLAMIDE;5-methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indole hydrochloride;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 | | CAS: | 158942-04-2 | | MF: | C17H16N4O | | MW: | 292.34 | | EINECS: | | | Product Categories: | Serotonin receptor;pharmacetical | | Mol File: | 158942-04-2.mol | ![5-Methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo [2,3-f]indole Structure](CAS/GIF/158942-04-2.gif) |
| | 5-Methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo [2,3-f]indole Chemical Properties |
| 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 | | Water Solubility | H2O: >10mg/mL | | InChI | 1S/C17H16N4O.ClH.H2O/c1-20-7-4-12-10-16-13(9-15(12)20)5-8-21(16)17(22)19-14-3-2-6-18-11-14;;/h2-4,6-7,9-11H,5,8H2,1H3,(H,19,22);1H;1H2 | | InChIKey | NXGFRKQJHLVHIT-UHFFFAOYSA-N | | SMILES | O.Cl.Cn1ccc2cc3N(CCc3cc12)C(=O)Nc4cccnc4 |
| WGK Germany | 3 | | Storage Class | 13 - Non Combustible Solids |
| | 5-Methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo [2,3-f]indole Usage And Synthesis |
| 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 . |
| | 5-Methyl-1-(3-pyridylcarbamoyl)-1,2,3,5-tetrahydropyrrolo [2,3-f]indole Preparation Products And Raw materials |
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