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
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
Molecular Formula | C20H29FN2O3 |
Molecular Weight | 364.4543 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
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 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:28:38 GMT 2023
by
admin
on
Sat Dec 16 08:28:38 GMT 2023
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Record UNII |
G9FWZ369GX
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Record Status |
Validated (UNII)
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Record Version |
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-
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Systematic Name | English |
Code System | Code | Type | Description | ||
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Fallypride
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G9FWZ369GX
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166173-78-0
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10021692
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DB15167
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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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