Details
Stereochemistry | ACHIRAL |
Molecular Formula | C19H29N5O2 |
Molecular Weight | 359.4659 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1(C)CC(=O)N(CCCCN2CCN(CC2)C3=NC=CC=N3)C(=O)C1
InChI
InChIKey=QOIGKGMMAGJZNZ-UHFFFAOYSA-N
InChI=1S/C19H29N5O2/c1-19(2)14-16(25)24(17(26)15-19)9-4-3-8-22-10-12-23(13-11-22)18-20-6-5-7-21-18/h5-7H,3-4,8-15H2,1-2H3
Gepirone (brand name Travivo) is an investigational azapirone antidepressant and anxiolytic drug in development for the treatment of major depressive disorder but has yet to be marketed. Like other azapirones, it acts as a selective partial agonist of the 5-HT1A receptor. Gepirone has been under development in the U.S. in an extended release form (referred to as Gepirone ER). It has been rejected multiple times by the FDA during the drug approval process and Phase III studies evaluating its use in the treatment of MDD were prematurely terminated. These were the initial Phase III studies of gepirone ER in MDD, and the effective dose range had not been determined. In March 2016, the FDA reversed its decision and gave gepirone ER a positive review, clearing the way for the drug to finally gain market approval in the U.S. In addition to its antidepressant and anxiolytic properties, gepirone has been found to improve symptoms of sexual dysfunction in men and women, similarly to the marketed 5-HT1A receptor agonist flibanserin. The pro-sexual effects appear to be independent of its antidepressant and anxiolytic effects. Mechanism of action studies have demonstrated that gepirone possesses a much greater selectivity for 5-HT1A receptors over dopamine D2 receptors. Long-term studies have shown that gepirone has a differential action at presynaptic (agonist) and post-synaptic (partial agonist) 5-HT1A receptors. Treatment with gepirone ER
desensitizes presynaptic 5-HT1A receptors, which decreases serotonin autoregulatory inhibition and enhances activation of postsynaptic 5-HT1A receptors. As a partial agonist gepirone ER acts as an agonist when endogenous serotonin is not present and as an antagonist when endogenous serotonin is present. Overall, gepirone ER increases serotonin production when insufficient amounts are present, and decreases serotonin production when excess amounts are present. Gepirone has been tested in Phase II clinical trial as antidepressant medication for pharmacotherapy for cocaine dependent subjects.
Originator
Sources: http://www.theinfolist.com/php/SummaryGet.php?FindGo=Gepirone | https://www.ncbi.nlm.nih.gov/pubmed/11892924
Curator's Comment: Gepirone was originally developed by Bristol-Myers Squibb in 1986, but was out-licensed to Fabre-Kramer in 1993. # Bristol-Myers Squibb
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: P08908 Gene ID: 3350.0 Gene Symbol: HTR1A Target Organism: Homo sapiens (Human) |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Secondary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
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Strychnine seizure potentiation by azaspirodecanedione anxiolytics in rats. | 1988 Oct 18 |
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Effects of 5-HT1A agonists and 5-HT2 antagonists on haloperidol-induced dyskinesias in squirrel monkeys: no evidence for reciprocal 5-HT-dopamine interaction. | 1989 |
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Prenatal exposure to cocaine: effects on aggression in Sprague-Dawley rats. | 1994 May |
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The clinical pharmacology of depressive states. | 2002 Mar |
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Rigid analogues of buspirone and gepirone, 5-HT1A receptors partial agonists. | 2002 Nov |
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Influence of housing conditions on the effects of serotonergic drugs on feeding behavior in non-deprived rats. | 2003 |
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Is there a role for 5-HT1A agonists in the treatment of depression? | 2003 Feb 1 |
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Cellular consequences of stress and depression. | 2004 Jun |
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Sustained efficacy of gepirone-IR in major depressive disorder: a double-blind placebo substitution trial. | 2004 May-Jun |
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Relapse prevention with gepirone ER in outpatients with major depression. | 2005 Feb |
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Novel, flexible, and conformationally defined analogs of gepirone: synthesis and 5-HT1A, 5-HT2A, and D2 receptor activity. | 2005 Feb 15 |
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Remission rates with 3 consecutive antidepressant trials: effectiveness for depressed outpatients. | 2005 Jun |
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Early response and 8-week treatment outcome in GAD. | 2006 |
Sample Use Guides
Gepirone ER (20 mg to 80 mg) was administered once per day in the morning for 8 weeks (56 days). Patients with moderate to severe depression initiated treatment by taking a 20 mg tablet once daily in the morning with food, followed by an increase to 40 mg daily between days 4 and 7. The dose could be increased to 60 mg daily after day 7, and to 80 mg daily after 14 days.
Route of Administration:
Oral
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ACTIVE MOIETY
METABOLITE (PARENT)
SALT/SOLVATE (PARENT)