Linopirdine: Difference between revisions
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Script assisted update of identifiers from ChemSpider, CommonChemistry and FDA for the Chem/Drugbox validation project - Updated: InChI1->InChI StdInChI StdInChIKey. |
Updating {{drugbox}} (no changed fields - added verified revid - updated 'UNII_Ref', 'ChemSpiderID_Ref', 'StdInChI_Ref', 'StdInChIKey_Ref') per Chem/Drugbox validation (report [[Wikipedia talk:Wi |
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{{drugbox |
{{drugbox |
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| verifiedrevid = 400143400 |
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| IUPAC_name = 1-phenyl-3,3-bis(pyridin-4-ylmethyl)-1,3-dihydro-2''H''-indol-2-one |
| IUPAC_name = 1-phenyl-3,3-bis(pyridin-4-ylmethyl)-1,3-dihydro-2''H''-indol-2-one |
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| image = Linopirdine.png |
| image = Linopirdine.png |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 3795 |
| ChemSpiderID = 3795 |
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| InChI = 1/C26H21N3O/c30-25-26(18-20-10-14-27-15-11-20,19-21-12-16-28-17-13-21)23-8-4-5-9-24(23)29(25)22-6-2-1-3-7-22/h1-17H,18-19H2 |
| InChI = 1/C26H21N3O/c30-25-26(18-20-10-14-27-15-11-20,19-21-12-16-28-17-13-21)23-8-4-5-9-24(23)29(25)22-6-2-1-3-7-22/h1-17H,18-19H2 |
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| InChIKey = YEJCDKJIEMIWRQ-UHFFFAOYAH |
| InChIKey = YEJCDKJIEMIWRQ-UHFFFAOYAH |
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| smiles = O=C2N(c1ccccc1C2(Cc3ccncc3)Cc4ccncc4)c5ccccc5 |
| smiles = O=C2N(c1ccccc1C2(Cc3ccncc3)Cc4ccncc4)c5ccccc5 |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI = 1S/C26H21N3O/c30-25-26(18-20-10-14-27-15-11-20,19-21-12-16-28-17-13-21)23-8-4-5-9-24(23)29(25)22-6-2-1-3-7-22/h1-17H,18-19H2 |
| StdInChI = 1S/C26H21N3O/c30-25-26(18-20-10-14-27-15-11-20,19-21-12-16-28-17-13-21)23-8-4-5-9-24(23)29(25)22-6-2-1-3-7-22/h1-17H,18-19H2 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = YEJCDKJIEMIWRQ-UHFFFAOYSA-N |
| StdInChIKey = YEJCDKJIEMIWRQ-UHFFFAOYSA-N |
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| CAS_number = 105431-72-9 |
| CAS_number = 105431-72-9 |
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Revision as of 16:24, 2 December 2010
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| Chemical and physical data | |
| Formula | C26H21N3O |
| Molar mass | 391.465 g/mol g·mol−1 |
| 3D model (JSmol) | |
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Linopirdine is a psychostimulant/nootropic, which has neuroprotective effects. It acts as a potassium channel blocker, and releases acetylcholine, which is probably responsible for its nootropic action.
See also
References
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