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Details

Stereochemistry ACHIRAL
Molecular Formula C24H29NO2
Molecular Weight 363.4926
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of F-15063

SMILES

CC1(C)CC2=CC=CC(OCCNCC3=CC=CC(=C3)C4=CCCC4)=C2O1

InChI

InChIKey=RAIDOKRWKAIHOH-UHFFFAOYSA-N
InChI=1S/C24H29NO2/c1-24(2)16-21-11-6-12-22(23(21)27-24)26-14-13-25-17-18-7-5-10-20(15-18)19-8-3-4-9-19/h5-8,10-12,15,25H,3-4,9,13-14,16-17H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C24H29NO2
Molecular Weight 363.4926
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Towards a new generation of potential antipsychotic agents combining D2 and 5-HT1A receptor activities.
2007 Feb 22
Induction by antipsychotics of "win-shift" in the drug discrimination paradigm.
2007 Jul
F15063, a potential antipsychotic with dopamine D(2)/D(3) antagonist, 5-HT(1A) agonist and D(4) partial agonist properties: (IV) duration of brain D2-like receptor occupancy and antipsychotic-like activity versus plasma concentration in mice.
2007 Jun
F15063, a potential antipsychotic with D2/D3 antagonist, 5-HT 1A agonist and D4 partial agonist properties. I. In vitro receptor affinity and efficacy profile.
2007 May
F15063, a compound with D2/D3 antagonist, 5-HT 1A agonist and D4 partial agonist properties. II. Activity in models of positive symptoms of schizophrenia.
2007 May
F15063, a compound with D2/D3 antagonist, 5-HT 1A agonist and D4 partial agonist properties. III. Activity in models of cognition and negative symptoms.
2007 May
Optimisation of anti-psychotic therapeutics: a balancing act?
2007 May
Antipsychotics differ in their ability to internalise human dopamine D2S and human serotonin 5-HT1A receptors in HEK293 cells.
2008 Feb 26
The antipsychotics clozapine and olanzapine increase plasma glucose and corticosterone levels in rats: comparison with aripiprazole, ziprasidone, bifeprunox and F15063.
2008 Sep 11
F15063, a potential antipsychotic with dopamine D2/D3 receptor antagonist, 5-HT1A receptor agonist and dopamine D4 receptor partial agonist properties: influence on neuronal firing and neurotransmitter release.
2009 Apr 1
Differences among conventional, atypical and novel putative D(2)/5-HT(1A) antipsychotics on catalepsy-associated behaviour in cynomolgus monkeys.
2009 Nov 5
F15063, a potential antipsychotic with dopamine D(2)/D(3) receptor antagonist and 5-HT(1A) receptor agonist properties: influence on immediate-early gene expression in rat prefrontal cortex and striatum.
2009 Oct 12
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 11:05:10 UTC 2023
Edited
by admin
on Sat Dec 16 11:05:10 UTC 2023
Record UNII
115OSL8W3F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
F-15063
Common Name English
(2-(2,2-DIMETHYL-2,3-DIHYDROBENZOFURAN-7-YLOXY)ETHYL)(3-(CYCLOPENTEN-1-YL)BENZYL)AMINE
Systematic Name English
BENZENEMETHANAMINE, 3-(1-CYCLOPENTEN-1-YL)-N-(2-((2,3-DIHYDRO-2,2-DIMETHYL-7-BENZOFURANYL)OXY)ETHYL)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID001336131
Created by admin on Sat Dec 16 11:05:10 UTC 2023 , Edited by admin on Sat Dec 16 11:05:10 UTC 2023
PRIMARY
PUBCHEM
10248159
Created by admin on Sat Dec 16 11:05:10 UTC 2023 , Edited by admin on Sat Dec 16 11:05:10 UTC 2023
PRIMARY
CAS
680203-70-7
Created by admin on Sat Dec 16 11:05:10 UTC 2023 , Edited by admin on Sat Dec 16 11:05:10 UTC 2023
PRIMARY
WIKIPEDIA
F-15063
Created by admin on Sat Dec 16 11:05:10 UTC 2023 , Edited by admin on Sat Dec 16 11:05:10 UTC 2023
PRIMARY
CAS
936029-03-7
Created by admin on Sat Dec 16 11:05:10 UTC 2023 , Edited by admin on Sat Dec 16 11:05:10 UTC 2023
SUPERSEDED
FDA UNII
115OSL8W3F
Created by admin on Sat Dec 16 11:05:10 UTC 2023 , Edited by admin on Sat Dec 16 11:05:10 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY