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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H29FN2O3
Molecular Weight 364.4543
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FALLYPRIDE

SMILES

COC1=CC(CCCF)=CC(C(=O)NC[C@@H]2CCCN2CC=C)=C1OC

InChI

InChIKey=OABRYNHZQBZDMG-INIZCTEOSA-N
InChI=1S/C20H29FN2O3/c1-4-10-23-11-6-8-16(23)14-22-20(24)17-12-15(7-5-9-21)13-18(25-2)19(17)26-3/h4,12-13,16H,1,5-11,14H2,2-3H3,(H,22,24)/t16-/m0/s1

HIDE SMILES / InChI
Fallypride is a high-affinity antagonist of dopamine D2 and D3 receptors. 18F-radiolabeled fallypride is used as a PET tracer to characterize D2/D3 receptors in the brain.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P14416
Gene ID: 1813.0
Gene Symbol: DRD2
Target Organism: Homo sapiens (Human)
2.1 nM [Ki]
Target ID: P35462
Gene ID: 1814.0
Gene Symbol: DRD3
Target Organism: Homo sapiens (Human)
1.6 nM [Ki]
PubMed

PubMed

TitleDatePubMed
Fluorinated benzamide neuroleptics--III. Development of (S)-N-[(1-allyl-2-pyrrolidinyl)methyl]-5-(3-[18F]fluoropropyl)-2, 3-dimethoxybenzamide as an improved dopamine D-2 receptor tracer.
1995 Apr
PET tracers for imaging of the dopaminergic system.
2006
In vitro affinities of various halogenated benzamide derivatives as potential radioligands for non-invasive quantification of D(2)-like dopamine receptors.
2007 Nov 1
Dopamine D3 receptor binding of (18)F-fallypride: Evaluation using in vitro and in vivo PET imaging studies.
2015 Dec
Name Type Language
FALLYPRIDE
Common Name English
BENZAMIDE, 5-(3-FLUOROPROPYL)-2,3-DIMETHOXY-N-(((2S)-1-(2-PROPEN-1-YL)-2-PYRROLIDINYL)METHYL)-
Systematic Name English
Code System Code Type Description
WIKIPEDIA
Fallypride
Created by admin on Sat Dec 16 08:28:38 GMT 2023 , Edited by admin on Sat Dec 16 08:28:38 GMT 2023
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FDA UNII
G9FWZ369GX
Created by admin on Sat Dec 16 08:28:38 GMT 2023 , Edited by admin on Sat Dec 16 08:28:38 GMT 2023
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CAS
166173-78-0
Created by admin on Sat Dec 16 08:28:38 GMT 2023 , Edited by admin on Sat Dec 16 08:28:38 GMT 2023
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PUBCHEM
10021692
Created by admin on Sat Dec 16 08:28:38 GMT 2023 , Edited by admin on Sat Dec 16 08:28:38 GMT 2023
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DRUG BANK
DB15167
Created by admin on Sat Dec 16 08:28:38 GMT 2023 , Edited by admin on Sat Dec 16 08:28:38 GMT 2023
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EPA CompTox
DTXSID30937173
Created by admin on Sat Dec 16 08:28:38 GMT 2023 , Edited by admin on Sat Dec 16 08:28:38 GMT 2023
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