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1.
Appl Radiat Isot ; 147: 211-214, 2019 May.
Article in English | MEDLINE | ID: mdl-30999206

ABSTRACT

An efficient method is described to tritiate spiperone at high specific activity.


Subject(s)
Spiperone/chemistry , Tritium/chemistry , Catalysis , Magnetic Resonance Spectroscopy/methods , Radioligand Assay , Spectrometry, Mass, Electrospray Ionization
2.
Appl Radiat Isot ; 65(7): 827-30, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17442578

ABSTRACT

Methods are presented to synthesize and characterize [methylene-3H] haloperidol 2 and [N-methyl-3H]trifluoperazine 6.


Subject(s)
Antipsychotic Agents/chemical synthesis , Haloperidol/chemical synthesis , Trifluoperazine/chemical synthesis , Tritium/chemistry , Haloperidol/analogs & derivatives , Magnetic Resonance Spectroscopy
4.
Appl Radiat Isot ; 58(4): 477-9, 2003 Apr.
Article in English | MEDLINE | ID: mdl-12672627

ABSTRACT

Gamma-aminobutyric acid was labelled with tritium by the tritium gas catalytic reduction of a convenient 4-aminotetrolic acid derivative. The purified product was characterized by HPLC and tritium NMR.


Subject(s)
Tritium/chemistry , gamma-Aminobutyric Acid/chemistry , Aminobutyrates/chemistry , Catalysis , Chromatography, High Pressure Liquid , Isotope Labeling , Magnetic Resonance Spectroscopy/methods , Oxidation-Reduction , gamma-Aminobutyric Acid/metabolism
5.
Appl Radiat Isot ; 57(3): 343-5, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12201140

ABSTRACT

To study its mechanism of antimalarial action, a tritium labelled analogue of (+/-)-chloroquine was required at high specific activity. Two synthetic methods were successfully employed. [3-3H] (+/-)-Chloroquine 2 was prepared by the catalytic tritium dehalogenation of an iodo precursor and [N-ethyl-3H] (+/-)-chloroquine 4 was synthesized by the alkylation of (+/-)-desethylchloroquine with [3H] ethyl iodide.


Subject(s)
Antimalarials/chemical synthesis , Chloroquine/chemical synthesis , Tritium/chemistry , Antimalarials/chemistry , Chloroquine/chemistry , Drug Design , Humans , Magnetic Resonance Spectroscopy , Stereoisomerism
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