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Details

Stereochemistry ACHIRAL
Molecular Formula C19H21ClF2N4O.C4H4O4
Molecular Weight 510.918
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of F-15599 FUMARATE

SMILES

OC(=O)\C=C\C(O)=O.CC1=CN=C(CNCC2(F)CCN(CC2)C(=O)C3=CC=C(F)C(Cl)=C3)N=C1

InChI

InChIKey=GNFUCNCQCSGZJH-WLHGVMLRSA-N
InChI=1S/C19H21ClF2N4O.C4H4O4/c1-13-9-24-17(25-10-13)11-23-12-19(22)4-6-26(7-5-19)18(27)14-2-3-16(21)15(20)8-14;5-3(6)1-2-4(7)8/h2-3,8-10,23H,4-7,11-12H2,1H3;1-2H,(H,5,6)(H,7,8)/b;2-1+

HIDE SMILES / InChI

Molecular Formula C4H4O4
Molecular Weight 116.0722
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Molecular Formula C19H21ClF2N4O
Molecular Weight 394.846
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

F-15599 is a novel agonist with high selectivity and efficacy at serotonin 5-HT(1A) receptors. In signal transduction, electrophysiological and neurochemical tests, F-15599 preferentially activates post-synaptic 5-HT(1A)Rs in rat frontal cortex. Such a profile may translate to an improved profile of therapeutic activity for mood disorders. [(18)F]F-15599 is a radiofluorinated agonist presenting interesting characteristics for probing in vitro and in vivo the high-affinity states of the 5-HT(1A) receptors. The Rett Syndrome Research Trust awarded a grant to Neurolixis to advance F-15599 to clinical development.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P08908
Gene ID: 3350.0
Gene Symbol: HTR1A
Target Organism: Homo sapiens (Human)
3.4 nM [Ki]
PubMed

PubMed

TitleDatePubMed
High-efficacy 5-HT1A agonists for antidepressant treatment: a renewed opportunity.
2007 Oct 4
Signal transduction and functional selectivity of F15599, a preferential post-synaptic 5-HT1A receptor agonist.
2009 Jan
Preferential in vivo action of F15599, a novel 5-HT(1A) receptor agonist, at postsynaptic 5-HT(1A) receptors.
2010 Aug
[18F]F15599, a novel 5-HT1A receptor agonist, as a radioligand for PET neuroimaging.
2010 Mar
F15599, a highly selective post-synaptic 5-HT(1A) receptor agonist: in-vivo profile in behavioural models of antidepressant and serotonergic activity.
2010 Nov
F15599, a preferential post-synaptic 5-HT1A receptor agonist: activity in models of cognition in comparison with reference 5-HT1A receptor agonists.
2010 Sep
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 20:05:34 GMT 2023
Edited
by admin
on Fri Dec 15 20:05:34 GMT 2023
Record UNII
7LQS8HJO6C
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
F-15599 FUMARATE
Common Name English
F-15,599 FUMARATE
Code English
NLX-101 FUMARATE
Code English
4-PIPERIDINEMETHANAMINE, 1-(3-CHLORO-4-FLUOROBENZOYL)-4-FLUORO-N-((5-METHYL-2-PYRIMIDINYL)METHYL)-, (2E)-2-BUTENEDIOATE (1:1)
Systematic Name English
Code System Code Type Description
CAS
635323-96-5
Created by admin on Fri Dec 15 20:05:34 GMT 2023 , Edited by admin on Fri Dec 15 20:05:34 GMT 2023
PRIMARY
PUBCHEM
119025643
Created by admin on Fri Dec 15 20:05:34 GMT 2023 , Edited by admin on Fri Dec 15 20:05:34 GMT 2023
PRIMARY
EVMPD
SUB197522
Created by admin on Fri Dec 15 20:05:34 GMT 2023 , Edited by admin on Fri Dec 15 20:05:34 GMT 2023
PRIMARY
FDA UNII
7LQS8HJO6C
Created by admin on Fri Dec 15 20:05:34 GMT 2023 , Edited by admin on Fri Dec 15 20:05:34 GMT 2023
PRIMARY
SMS_ID
100000183188
Created by admin on Fri Dec 15 20:05:34 GMT 2023 , Edited by admin on Fri Dec 15 20:05:34 GMT 2023
PRIMARY
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ACTIVE MOIETY