Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Amber Thaxton"'
Autor:
Forrest Smith, Karim M. Abdel-Hay, Logan Neel, Amber Thaxton-Weissenfluh, C. Randall Clark, Jack DeRuiter, Tarek S. Belal, Lewis W. Smith, Younis Abiedalla
Publikováno v:
Forensic Chemistry. 12:78-90
The compounds in this study are the six regioisomeric 2-, 3-, 4-, 5-, 6- and 7-formyl indoles and the corresponding six regioisomeric N-n-pentylindole aldehydes. These compounds can serve as precursor chemicals and synthetic intermediates for a numbe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a788729eb213d19d68bb6ac2d601262
https://doi.org/10.1016/j.forc.2018.12.004
https://doi.org/10.1016/j.forc.2018.12.004
Autor:
Lewis W. Smith, C. Randall Clark, Younis Abiedalla, Amber Thaxton-Weissenfluh, Jack DeRuiter, Forrest Smith
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 196:375-384
The twelve 1-n-pentyl-2-, 3-, 4-, 5-, 6- and 7-(1- and 2-naphthoyl)-indoles each have the same substituents attached to the indole ring, identical elemental composition (C24H23NO) yielding identical nominal and accurate masses. These twelve isomers c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::520df0b32dfcd64d05b476e9f88e315b
https://doi.org/10.1016/j.saa.2018.02.052
https://doi.org/10.1016/j.saa.2018.02.052
Autor:
Jack DeRuiter, C. Randall Clark, Forrest Smith, Younis Abiedalla, Amber Thaxton-Weissenfluh, Amsha S. Alsegiani
Publikováno v:
Journal of Chromatography B. :77-84
The six 1-n-pentyl-2-, 3-, 4-, 5-, 6- and 7-(2-naphthoyl)-indoles each have the same substituents attached to the indole ring, identical elemental composition (C24H23NO) yielding identical nominal and accurate masses. The electron ionization mass spe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::149be8504dfb1c1bcf5611622aac3466
https://doi.org/10.1016/j.jchromb.2018.01.036
https://doi.org/10.1016/j.jchromb.2018.01.036
Autor:
C. Randall Clark, Tarek S. Belal, Forrest Smith, Jack DeRuiter, Karim M. Abdel-Hay, Amber Thaxton-Weissenfluh, Younis Abiedalla
Publikováno v:
Forensic Chemistry. 7:1-9
The five regioisomeric methylated indole ring analogues of JWH-018 can be prepared directly from a common set of precursor materials. These five isomers include 2-methyl-1-n-pentyl-3-(1-naphthoyl)-indole (JWH-007) and its four regioisomeric analogues
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aed67f3c3e7ba2dabc97dac8bdb0df9e
https://doi.org/10.1016/j.forc.2017.11.001
https://doi.org/10.1016/j.forc.2017.11.001
Autor:
Forrest Smith, Jack De Ruiter, Amber Thaxton-Weissenfluh, Karim M. Abdel-Hay, Amsha S. Alsegiani, C. Randall Clark
Publikováno v:
Journal of Pharmaceutical and Biomedical Analysis. 125:360-368
The six regioisomeric 1-pentyl-3-dimethoxybenzoylindoles can be differentiated by a combination of EI-MS and FT-IR spectra. The six regioisomeric 1-n-pentyl-3-(dimethoxybenzoyl)-indoles represent potential designer modifications in the synthetic cann
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0054eedda3ce5b7c26dfdee408021cd1
https://doi.org/10.1016/j.jpba.2016.04.012
https://doi.org/10.1016/j.jpba.2016.04.012
Autor:
Jack DeRuiter, C. Randall Clark, Karim M. Abdel-Hay, Tarek S. Belal, Forrest Smith, Amber Thaxton-Weissenfluh, Younis Abiedalla
Publikováno v:
Applied spectroscopy. 73(4)
The analytical differentiation of the indole ring regioisomeric chloro-1- n-pentyl-3-(1-naphthoyl)-indoles is described in this report. The regioisomeric chloroindole precursor compounds, N- n-pentyl chloroindole synthetic intermediates, and the targ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::416c790db06a9a13bfd4665b093acd0c
https://pubmed.ncbi.nlm.nih.gov/30347999
https://pubmed.ncbi.nlm.nih.gov/30347999
Autor:
C. Randall Clark, Jack DeRuiter, Tarek S. Belal, Amber Thaxton, Forrest Smith, Karim M. Abdel-Hay
Publikováno v:
Rapid Communications in Mass Spectrometry. 29:871-877
Rationale A number of synthetic cannabinoids such as the 1-alkyl-3-acylindoles are the target of significant designer drug activity. One of the first waves of these compounds identified in clandestine samples was 1-n-pentyl-3-(1-naphthoyl)indole, JWH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15164e0a657e263ffb4a6501cd830caf
https://doi.org/10.1002/rcm.7171
https://doi.org/10.1002/rcm.7171
Autor:
Forrest Smith, Younis Abiedalla, Jack DeRuiter, Tarek S. Belal, C. Randall Clark, Karim M. Abdel-Hay, Logan Neel, Amber Thaxton-Weissenfluh
Publikováno v:
Journal of chromatographic science. 56(9)
The indole ring regioisomeric methoxy-1-n-pentyl-3-(1-naphthoyl)-indoles represent indole ring-substituted analogs of the synthetic cannabinoid JWH-018. The electron ionization mass spectra show equivalent regioisomeric major fragments resulting from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83e0e4792ed2cb46d8a7d42240a54fde
https://pubmed.ncbi.nlm.nih.gov/29920587
https://pubmed.ncbi.nlm.nih.gov/29920587
Autor:
Amber, Thaxton, Tarek S, Belal, Forrest, Smith, Jack, DeRuiter, Karim M, Abdel-Hay, C Randall, Clark
Publikováno v:
Rapid communications in mass spectrometry : RCM. 29(9)
A number of synthetic cannabinoids such as the 1-alkyl-3-acylindoles are the target of significant designer drug activity. One of the first waves of these compounds identified in clandestine samples was 1-n-pentyl-3-(1-naphthoyl)indole, JWH-018. Thes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1417d7df62c5b97911a1444e14accbd7
https://pubmed.ncbi.nlm.nih.gov/26377015
https://pubmed.ncbi.nlm.nih.gov/26377015
Autor:
Sari Izenwasser, Stacey A. Lomenzo, Mark L. Trudell, Vivian R. Jaber, Amber Thaxton, Edwin D. Stevens, David L. Mobley, Dean Wade
Publikováno v:
Bioorganicmedicinal chemistry letters. 23(15)
A series of 3-aryl-3-arylmethoxy-azetidines were synthesized and evaluated for binding affinities at dopamine and serotonin transporters. The 3-aryl-3-arylmethoxyazetidines were generally SERT selective with the dichloro substituted congener 7c (Ki =
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fea5677f55424561116bfaae55e1d199
https://pubmed.ncbi.nlm.nih.gov/23806554
https://pubmed.ncbi.nlm.nih.gov/23806554