Ipsapirone
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| Routes of administration | Oral |
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| Elimination half-life | 1.3-2.7 hours |
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| Formula | C19H23N5O3S |
| Molar mass | 401.49 g·mol−1 |
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Ipsapirone is a selective 5-HT1A receptor partial agonist of the piperazine and azapirone chemical classes.[1] It has antidepressant and anxiolytic effects.[1] Ipsapirone was studied in several placebo-controlled trials for depression and continues to be used in research.[2]
See also
References
- 1 2 Fanelli RJ, Schuurman T, Glaser T, Traber J (1990). "Ipsapirone: a novel anxiolytic and selective 5-HT1A receptor ligand". Progress in Clinical and Biological Research. 361: 461–7. PMID 1981264.
- ↑ Chessick, Cheryl A.; Allen, Michael H.; Thase, Michael E.; Batista Miralha Da Cunha, Angelo ABC; Kapczinski, Flávio; Silva De Lima, Mauricio; Dos Santos Souza, Juliano JSS (Jul 19, 2006). "Azapirones for generalized anxiety disorder". Cochrane Database Syst Rev (3): CD006115. doi:10.1002/14651858.CD006115. PMID 16856115.
| 5-HT1AR agonists | |
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| GABAAR PAMs |
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| Gabapentinoids (α2δ VDCC blockers) | |
| Antidepressants |
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| Sympatholytics (Antiadrenergics) |
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| Simple piperazines (no additional rings) |
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| Phenylpiperazines |
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| Benzylpiperazines | |
| Diphenylalkylpiperazines (benzhydrylalkylpiperazines) |
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| Pyrimidinylpiperazines |
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| Pyridinylpiperazines |
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| Benzo(iso)thiazolylpiperazines | |
| Tricyclics (piperazine attached via side chain) |
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| Others/Uncategorized |
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