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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
Structure of GEPIRONE

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

HIDE SMILES / InChI

Description

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.

CNS Activity

Originator

Approval Year

Targets

Primary TargetPharmacologyConditionPotency

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Cmax

ValueDoseCo-administeredAnalytePopulation
2.55 ng/mL
20 mg single, oral
GEPIRONE plasma
Homo sapiens
4.13 ng/mL
20 mg single, oral
GEPIRONE plasma
Homo sapiens
3.21 ng/mL
20 mg single, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
2.8 ng/mL
20 mg single, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
6.54 ng/mL
20 mg single, oral
3-HYDROXYGEPIRONE plasma
Homo sapiens
7.69 ng/mL
20 mg single, oral
3-HYDROXYGEPIRONE plasma
Homo sapiens
6.1 ng/mL
10 mg 2 times / day multiple, oral
GEPIRONE plasma
Homo sapiens
6.3 ng/mL
10 mg 2 times / day multiple, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
4.3 ng/mL
20 mg 1 times / day multiple, oral
GEPIRONE plasma
Homo sapiens
4.2 ng/mL
20 mg 1 times / day multiple, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
3.6 ng/mL
25 mg 1 times / day multiple, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
3.6 ng/mL
25 mg 1 times / day multiple, oral
GEPIRONE plasma
Homo sapiens
18.73 ng/mL
20 mg single, oral
GEPIRONE plasma
Homo sapiens
12.03 ng/mL
20 mg single, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
12.55 ng/mL
20 mg single, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
16.98 ng/mL
20 mg single, oral
GEPIRONE plasma
Homo sapiens

AUC

ValueDoseCo-administeredAnalytePopulation
31.14 ng × h/mL
20 mg single, oral
GEPIRONE plasma
Homo sapiens
38.71 ng × h/mL
20 mg single, oral
GEPIRONE plasma
Homo sapiens
52.77 ng × h/mL
20 mg single, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
55.39 ng × h/mL
20 mg single, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
138 ng × h/mL
20 mg single, oral
3-HYDROXYGEPIRONE plasma
Homo sapiens
157 ng × h/mL
20 mg single, oral
3-HYDROXYGEPIRONE plasma
Homo sapiens
54.9 ng × h/mL
10 mg 2 times / day multiple, oral
GEPIRONE plasma
Homo sapiens
92.8 ng × h/mL
10 mg 2 times / day multiple, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
55.3 ng × h/mL
20 mg 1 times / day multiple, oral
GEPIRONE plasma
Homo sapiens
74 ng × h/mL
20 mg 1 times / day multiple, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
67.6 ng × h/mL
25 mg 1 times / day multiple, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
51.8 ng × h/mL
25 mg 1 times / day multiple, oral
GEPIRONE plasma
Homo sapiens
55.26 ng × h/mL
20 mg single, oral
GEPIRONE plasma
Homo sapiens
93 ng × h/mL
20 mg single, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
99.2 ng × h/mL
20 mg single, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
75.69 ng × h/mL
20 mg single, oral
GEPIRONE plasma
Homo sapiens

T1/2

ValueDoseCo-administeredAnalytePopulation
2.94 h
20 mg single, oral
GEPIRONE plasma
Homo sapiens
5.76 h
20 mg single, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
6.06 h
20 mg single, oral
1-(2-PYRIMIDINYL)PIPERAZINE plasma
Homo sapiens
3.32 h
20 mg single, oral
GEPIRONE plasma
Homo sapiens

Doses

AEs

OverviewOther

Other InhibitorOther SubstrateOther Inducer

Drug as perpetrator​

Drug as victim

PubMed

Sample Use Guides

In Vivo Use Guide
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
In Vitro Use Guide
Unknown