Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C24H29N5O2.ClH |
| Molecular Weight | 455.98 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 6 / 6 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.O=C1[C@H]2[C@H]([C@H]3C=C[C@@H]2[C@@H]4C=C[C@H]34)C(=O)N1CCCCN5CCN(CC5)C6=NC=CC=N6
InChI
InChIKey=XQINQMZXDOSBBV-FDPNZRBCSA-N
InChI=1S/C24H29N5O2.ClH/c30-22-20-18-6-7-19(17-5-4-16(17)18)21(20)23(31)29(22)11-2-1-10-27-12-14-28(15-13-27)24-25-8-3-9-26-24;/h3-9,16-21H,1-2,10-15H2;1H/t16-,17+,18-,19+,20-,21+;
Zalospirone is a selective partial agonist of 5HT1A receptor developed by Wyeth. It was investigated in clinical trials in major depression. Although the highest dose of the drug seemed to have significant antidepressant efficacy, it was not well tolerated and by the 6th week more than half of patients in the high-dose group has dropped out.
Originator
Approval Year
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Preferred Name | English | ||
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Code | English | ||
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C47794
Created by
admin on Mon Mar 31 18:25:16 GMT 2025 , Edited by admin on Mon Mar 31 18:25:16 GMT 2025
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NCI_THESAURUS |
C28197
Created by
admin on Mon Mar 31 18:25:16 GMT 2025 , Edited by admin on Mon Mar 31 18:25:16 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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C067729
Created by
admin on Mon Mar 31 18:25:16 GMT 2025 , Edited by admin on Mon Mar 31 18:25:16 GMT 2025
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PRIMARY | |||
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CC-36
Created by
admin on Mon Mar 31 18:25:16 GMT 2025 , Edited by admin on Mon Mar 31 18:25:16 GMT 2025
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C72878
Created by
admin on Mon Mar 31 18:25:16 GMT 2025 , Edited by admin on Mon Mar 31 18:25:16 GMT 2025
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300000055452
Created by
admin on Mon Mar 31 18:25:16 GMT 2025 , Edited by admin on Mon Mar 31 18:25:16 GMT 2025
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PRIMARY | |||
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114374-97-9
Created by
admin on Mon Mar 31 18:25:16 GMT 2025 , Edited by admin on Mon Mar 31 18:25:16 GMT 2025
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PRIMARY | |||
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23725074
Created by
admin on Mon Mar 31 18:25:16 GMT 2025 , Edited by admin on Mon Mar 31 18:25:16 GMT 2025
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PRIMARY | |||
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CHEMBL2110887
Created by
admin on Mon Mar 31 18:25:16 GMT 2025 , Edited by admin on Mon Mar 31 18:25:16 GMT 2025
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PRIMARY | |||
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5IEH2KC4M6
Created by
admin on Mon Mar 31 18:25:16 GMT 2025 , Edited by admin on Mon Mar 31 18:25:16 GMT 2025
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PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD