2001 (v1)
Publication
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Uploaded on: March 31, 2023
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2000 (v1)Publication
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Uploaded on: April 14, 2023 -
2001 (v1)Publication
No description
Uploaded on: March 31, 2023 -
1999 (v1)Publication
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Uploaded on: December 4, 2022 -
2009 (v1)Publication
In order to further explore the antiproliferative properties of O-phenoxyethyl and O-adamantyl acylthiocarbamates (ATCs), a series of 14 derivs. was prepd. by a parallel adaptation of a highly convergent one-pot three-step procedure. Ten acylthiocarbamates were selected by the National Cancer Institute drug evaluation program and screened...
Uploaded on: March 25, 2023 -
2008 (v1)Publication
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Uploaded on: April 14, 2023 -
2006 (v1)Publication
In the crystal structure of the novel acylthiocarbamate derivative O-[2-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-ethyl] N-(4-methylphenyl)-N-(3-nitrobenzoyl)thiocarbamate, C25H19N3O6S, intra- and intermolecular pi-pi interactions occur between the phthalimide and N-benzoyl moieties. The partial atomic charges, calculated by ab initio methods,...
Uploaded on: May 13, 2023 -
2009 (v1)Publication
Acylthiocarbamates (ATCs) have been identified as a class of potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. A computational strategy based on molecular docking studies followed by comparative molecular fields analysis (CoMFA) and comparative molecular similarity indices analysis (CoMSIA) was used to identify the...
Uploaded on: April 14, 2023 -
2006 (v1)Publication
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Uploaded on: April 14, 2023 -
2009 (v1)Publication
Thiocarbamates (TCs) have been recently identified as a new class of potent non-nucleoside HIV-1 Reverse Transcriptase (RT) inhibitors. A computational strategy based on molecular docking studies, followed by CoMFA and CoMSIA analyses, has been used to elucidate the atomic details of the RT/TC interactions and to identify the most important...
Uploaded on: April 14, 2023