Synthesis of 131I derivatives of indolealkylamines for brain mapping

The synthesis and spectral properties of new radioiodinated indolealkylamines like 2-[131 I]-iodo-N,N-dimethyltryptamine, 2-[131 I]-iodo-N-methyltryptamine, 2-[131 I]-iodo-5-methoxy-N,N-dimethyltryptamine, 2-[131 I]-iodo-5-hydroxy-N,N-dimethyltryptamine (2-[131 I]-iodo-bufotenine), and 2-[131I]-iodo...

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Autores principales: Sintas, J.A., Vitale, A.A.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_03624803_v39_n8_p677_Sintas
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spelling todo:paper_03624803_v39_n8_p677_Sintas2023-10-03T15:27:08Z Synthesis of 131I derivatives of indolealkylamines for brain mapping Sintas, J.A. Vitale, A.A. 2-[131I]-iodo-5-hydroxy-N,N-dimethyltryptamine 2-[131I]-iodo-5-methoxy-N,N-dimethyltryptamine 2-[131I]-iodo-N,N-dimethyltryptamine 2-[131I]-iodo-N-methyltryptamine 2-[131I]-iodo-tryptamine 2-[131I]-melatonine indoleamine iodine 131 tryptamine derivative article brain mapping drug purity drug synthesis in vitro study iodination mass spectrometry nuclear magnetic resonance spectroscopy radiochemistry radioiodination reaction analysis The synthesis and spectral properties of new radioiodinated indolealkylamines like 2-[131 I]-iodo-N,N-dimethyltryptamine, 2-[131 I]-iodo-N-methyltryptamine, 2-[131 I]-iodo-5-methoxy-N,N-dimethyltryptamine, 2-[131 I]-iodo-5-hydroxy-N,N-dimethyltryptamine (2-[131 I]-iodo-bufotenine), and 2-[131I]-iodo-tryptamine and the known 2-[131I]-iodo-N-acetyl-5-methoxy-tryptamine (2-[131I]-iodo-melatonine) are described herein. These were synthesized by a high-yield novel method, and their spectral properties are fully described. These compounds are of biological importance and can be used for brain mapping with SPECT technology. Fil:Vitale, A.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03624803_v39_n8_p677_Sintas
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 2-[131I]-iodo-5-hydroxy-N,N-dimethyltryptamine
2-[131I]-iodo-5-methoxy-N,N-dimethyltryptamine
2-[131I]-iodo-N,N-dimethyltryptamine
2-[131I]-iodo-N-methyltryptamine
2-[131I]-iodo-tryptamine
2-[131I]-melatonine
indoleamine
iodine 131
tryptamine derivative
article
brain mapping
drug purity
drug synthesis
in vitro study
iodination
mass spectrometry
nuclear magnetic resonance spectroscopy
radiochemistry
radioiodination
reaction analysis
spellingShingle 2-[131I]-iodo-5-hydroxy-N,N-dimethyltryptamine
2-[131I]-iodo-5-methoxy-N,N-dimethyltryptamine
2-[131I]-iodo-N,N-dimethyltryptamine
2-[131I]-iodo-N-methyltryptamine
2-[131I]-iodo-tryptamine
2-[131I]-melatonine
indoleamine
iodine 131
tryptamine derivative
article
brain mapping
drug purity
drug synthesis
in vitro study
iodination
mass spectrometry
nuclear magnetic resonance spectroscopy
radiochemistry
radioiodination
reaction analysis
Sintas, J.A.
Vitale, A.A.
Synthesis of 131I derivatives of indolealkylamines for brain mapping
topic_facet 2-[131I]-iodo-5-hydroxy-N,N-dimethyltryptamine
2-[131I]-iodo-5-methoxy-N,N-dimethyltryptamine
2-[131I]-iodo-N,N-dimethyltryptamine
2-[131I]-iodo-N-methyltryptamine
2-[131I]-iodo-tryptamine
2-[131I]-melatonine
indoleamine
iodine 131
tryptamine derivative
article
brain mapping
drug purity
drug synthesis
in vitro study
iodination
mass spectrometry
nuclear magnetic resonance spectroscopy
radiochemistry
radioiodination
reaction analysis
description The synthesis and spectral properties of new radioiodinated indolealkylamines like 2-[131 I]-iodo-N,N-dimethyltryptamine, 2-[131 I]-iodo-N-methyltryptamine, 2-[131 I]-iodo-5-methoxy-N,N-dimethyltryptamine, 2-[131 I]-iodo-5-hydroxy-N,N-dimethyltryptamine (2-[131 I]-iodo-bufotenine), and 2-[131I]-iodo-tryptamine and the known 2-[131I]-iodo-N-acetyl-5-methoxy-tryptamine (2-[131I]-iodo-melatonine) are described herein. These were synthesized by a high-yield novel method, and their spectral properties are fully described. These compounds are of biological importance and can be used for brain mapping with SPECT technology.
format JOUR
author Sintas, J.A.
Vitale, A.A.
author_facet Sintas, J.A.
Vitale, A.A.
author_sort Sintas, J.A.
title Synthesis of 131I derivatives of indolealkylamines for brain mapping
title_short Synthesis of 131I derivatives of indolealkylamines for brain mapping
title_full Synthesis of 131I derivatives of indolealkylamines for brain mapping
title_fullStr Synthesis of 131I derivatives of indolealkylamines for brain mapping
title_full_unstemmed Synthesis of 131I derivatives of indolealkylamines for brain mapping
title_sort synthesis of 131i derivatives of indolealkylamines for brain mapping
url http://hdl.handle.net/20.500.12110/paper_03624803_v39_n8_p677_Sintas
work_keys_str_mv AT sintasja synthesisof131iderivativesofindolealkylaminesforbrainmapping
AT vitaleaa synthesisof131iderivativesofindolealkylaminesforbrainmapping
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