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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

Molecular Formula C19H29N5O2
Molecular Weight 359.4659
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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

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

Targets

Primary TargetPharmacologyConditionPotency
Conditions
PubMed

PubMed

TitleDatePubMed
Strychnine seizure potentiation by azaspirodecanedione anxiolytics in rats.
1988 Oct 18
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
Prenatal exposure to cocaine: effects on aggression in Sprague-Dawley rats.
1994 May
The clinical pharmacology of depressive states.
2002 Mar
5-HT1A receptor-mediated regulation of mitogen-activated protein kinase phosphorylation in rat brain.
2002 Oct 4
Differential effects of the 5-HT1A agonist gepirone on food intake in rats may depend on their motivation to eat.
2003 Nov
The design and preparation of metabolically protected new arylpiperazine 5-HT1A ligands.
2004 Apr 5
Metabolism of the newest antidepressants: comparisons with related predecessors.
2004 Feb
Cellular consequences of stress and depression.
2004 Jun
Sustained efficacy of gepirone-IR in major depressive disorder: a double-blind placebo substitution trial.
2004 May-Jun
The 5-HT1A receptor and the stimulus effects of LSD in the rat.
2005 Oct
Emotional reactivity and cognitive performance in aversively motivated tasks: a comparison between four rat strains.
2009 Dec 15
Practical application of cure mixture model for long-term censored survivor data from a withdrawal clinical trial of patients with major depressive disorder.
2010 Apr 23
Patents

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
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:59:51 UTC 2023
Edited
by admin
on Fri Dec 15 15:59:51 UTC 2023
Record UNII
JW5Y7B8Z18
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
GEPIRONE
INN   WHO-DD  
INN  
Official Name English
2,6-PIPERIDINEDIONE, 4,4-DIMETHYL-1-(4-(4-(2-PYRIMIDINYL)-1-PIPERAZINYL)BUTYL)-
Systematic Name English
gepirone [INN]
Common Name English
Gepirone [WHO-DD]
Common Name English
3,3-DIMETHYL-1-(4-(4-(2-PYRIMIDINYL)-1-PIPERAZINYL)BUTYL)GLUTARIMIDE
Common Name English
Classification Tree Code System Code
WHO-VATC QN06AX19
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
NCI_THESAURUS C47794
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
NCI_THESAURUS C28197
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
WHO-ATC N06AX19
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
Code System Code Type Description
INN
5676
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
SMS_ID
100000084522
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
PUBCHEM
55191
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
DRUG CENTRAL
4562
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
CAS
83928-76-1
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
EVMPD
SUB07897MIG
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
EPA CompTox
DTXSID90232813
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
DRUG BANK
DB12184
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
NCI_THESAURUS
C74193
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
WIKIPEDIA
GEPIRONE
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
MESH
C039979
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
FDA UNII
JW5Y7B8Z18
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
ChEMBL
CHEMBL284092
Created by admin on Fri Dec 15 15:59:51 UTC 2023 , Edited by admin on Fri Dec 15 15:59:51 UTC 2023
PRIMARY
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