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Details

Stereochemistry ACHIRAL
Molecular Formula C19H29N5O2.ClH
Molecular Weight 395.927
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GEPIRONE HYDROCHLORIDE

SMILES

Cl.CC1(C)CC(=O)N(CCCCN2CCN(CC2)C3=NC=CC=N3)C(=O)C1

InChI

InChIKey=DGOCVISYYYQFEP-UHFFFAOYSA-N
InChI=1S/C19H29N5O2.ClH/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;1H

HIDE SMILES / InChI
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
Prenatal exposure to cocaine: effects on aggression in Sprague-Dawley rats.
1994 May
Gepirone. Organon.
2001 Aug
Effects of serotonergic compounds on aqueous humor dynamics in monkeys.
2001 Aug
Rigid analogues of buspirone and gepirone, 5-HT1A receptors partial agonists.
2002 Nov
5-HT1A receptor-mediated regulation of mitogen-activated protein kinase phosphorylation in rat brain.
2002 Oct 4
Influence of housing conditions on the effects of serotonergic drugs on feeding behavior in non-deprived rats.
2003
Is there a role for 5-HT1A agonists in the treatment of depression?
2003 Feb 1
A review of the efficacy and tolerability of immediate-release and extended-release formulations of gepirone.
2003 Jun
Gepirone extended-release: new evidence for efficacy in the treatment of major depressive disorder.
2003 Mar
Human cytochromes mediating gepirone biotransformation at low substrate concentrations.
2003 Mar
Pharmacokinetic evaluation of gepirone immediate-release capsules and gepirone extended-release tablets in healthy volunteers.
2003 Sep
Assessing the neuronal serotonergic target-based antidepressant stratagem: impact of in vivo interaction studies and knockout models.
2008 Sep
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
Name Type Language
GEPIRONE HYDROCHLORIDE
DASH   MART.   USAN  
USAN  
Official Name English
3,3-Dimethyl-1-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]glutarimide monohydrochloride
Common Name English
GEPIRONE HYDROCHLORIDE [MART.]
Common Name English
GEPIRONE HCL
Common Name English
EXXUA
Brand Name English
Gepirone hydrochloride [WHO-DD]
Common Name English
BMY-13805-1
Code English
BMY 13805-1
Code English
TRAVIVO
Brand Name English
GEPIRONE HYDROCHLORIDE [USAN]
Common Name English
2,6-PIPERIDINEDIONE, 4,4-DIMETHYL-1-(4-(4-(2-PYRIMIDINYL)-1-PIPERAZINYL)BUTYL)-, MONOHYDROCHLORIDE
Common Name English
TGFK07AD
Code English
Classification Tree Code System Code
NCI_THESAURUS C28197
Created by admin on Fri Dec 15 15:29:55 GMT 2023 , Edited by admin on Fri Dec 15 15:29:55 GMT 2023
NCI_THESAURUS C47794
Created by admin on Fri Dec 15 15:29:55 GMT 2023 , Edited by admin on Fri Dec 15 15:29:55 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C72795
Created by admin on Fri Dec 15 15:29:55 GMT 2023 , Edited by admin on Fri Dec 15 15:29:55 GMT 2023
PRIMARY
PUBCHEM
55190
Created by admin on Fri Dec 15 15:29:55 GMT 2023 , Edited by admin on Fri Dec 15 15:29:55 GMT 2023
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EPA CompTox
DTXSID30232812
Created by admin on Fri Dec 15 15:29:55 GMT 2023 , Edited by admin on Fri Dec 15 15:29:55 GMT 2023
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DRUG BANK
DBSALT002148
Created by admin on Fri Dec 15 15:29:55 GMT 2023 , Edited by admin on Fri Dec 15 15:29:55 GMT 2023
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ChEMBL
CHEMBL284092
Created by admin on Fri Dec 15 15:29:55 GMT 2023 , Edited by admin on Fri Dec 15 15:29:55 GMT 2023
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CAS
83928-66-9
Created by admin on Fri Dec 15 15:29:55 GMT 2023 , Edited by admin on Fri Dec 15 15:29:55 GMT 2023
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USAN
W-38
Created by admin on Fri Dec 15 15:29:55 GMT 2023 , Edited by admin on Fri Dec 15 15:29:55 GMT 2023
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FDA UNII
80C9L8EP6V
Created by admin on Fri Dec 15 15:29:55 GMT 2023 , Edited by admin on Fri Dec 15 15:29:55 GMT 2023
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