A V Stachulski - JoVE Visualize

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Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 22, 2005

Development of novel furanocoumarin dimers as potent and selective inhibitors of CYP3A4E Row, S A Brown, A V Stachulski, et al.

Organic & Biomolecular Chemistry|April 11, 2006

Design, synthesis and evaluation of furanocoumarin monomers as inhibitors of CYP3A4E C Row, S A Brown, A V Stachulski, et al.

Bioorganic & Medicinal Chemistry|February 17, 2006

Synthesis of 8-geranyloxypsoralen analogues and their evaluation as inhibitors of CYP3A4E C Row, S A Brown, A V Stachulski, et al.

Journal of Medicinal Chemistry|April 20, 2001

Efficient preparations of the beta-glucuronides of dihydroartemisinin and structural confirmation of the human glucuronide metaboliteP M O'Neill, F Scheinmann, A V Stachulski, et al.

Veterinary Parasitology|April 17, 2009

In vitro efficacy of nitro- and halogeno-thiazolide/thiadiazolide derivatives against Sarcocystis neuronaG Gargala, L Le Goff, J J Ballet, et al.

International Journal of Peptide and Protein Research|January 1, 1979

Synthesis and biological activities of [7-(azetidine-2-carboxylic acid)]-oxytocin and -lysine-vasopressinM Barber, J H Jones, A V Stachulski, et al.

Xenobiotica; the Fate of Foreign Compounds in Biological Systems|November 19, 2009

Integrated HPLC-MS and (1)H-NMR spectroscopic studies on acyl migration reaction kinetics of model drug ester glucuronidesC H Johnson, E Karlsson, S Sarda, et al.

Journal of Medicinal Chemistry|January 5, 2001

Synthesis, antimalarial activity, biomimetic iron(II) chemistry, and in vivo metabolism of novel, potent C-10-phenoxy derivatives of dihydroartemisininP M O'Neill, A Miller, L P Bishop, et al.

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Drug Metabolism and Disposition: the Biological Fate of Chemicals|November 22, 2005

Development of novel furanocoumarin dimers as potent and selective inhibitors of CYP3A4E Row, S A Brown, A V Stachulski, et al.

Organic & Biomolecular Chemistry|April 11, 2006

Design, synthesis and evaluation of furanocoumarin monomers as inhibitors of CYP3A4E C Row, S A Brown, A V Stachulski, et al.

Bioorganic & Medicinal Chemistry|February 17, 2006

Synthesis of 8-geranyloxypsoralen analogues and their evaluation as inhibitors of CYP3A4E C Row, S A Brown, A V Stachulski, et al.

Journal of Medicinal Chemistry|April 20, 2001

Efficient preparations of the beta-glucuronides of dihydroartemisinin and structural confirmation of the human glucuronide metaboliteP M O'Neill, F Scheinmann, A V Stachulski, et al.

Veterinary Parasitology|April 17, 2009

In vitro efficacy of nitro- and halogeno-thiazolide/thiadiazolide derivatives against Sarcocystis neuronaG Gargala, L Le Goff, J J Ballet, et al.

International Journal of Peptide and Protein Research|January 1, 1979

Synthesis and biological activities of [7-(azetidine-2-carboxylic acid)]-oxytocin and -lysine-vasopressinM Barber, J H Jones, A V Stachulski, et al.

Xenobiotica; the Fate of Foreign Compounds in Biological Systems|November 19, 2009

Integrated HPLC-MS and (1)H-NMR spectroscopic studies on acyl migration reaction kinetics of model drug ester glucuronidesC H Johnson, E Karlsson, S Sarda, et al.

Journal of Medicinal Chemistry|January 5, 2001

Synthesis, antimalarial activity, biomimetic iron(II) chemistry, and in vivo metabolism of novel, potent C-10-phenoxy derivatives of dihydroartemisininP M O'Neill, A Miller, L P Bishop, et al.

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