Fluorine and chlorine substituted adamantyl-urea as molecular tools for inhibition of human soluble epoxide hydrolase with picomolar efficacy

Vladimir V. Burmistrova Volgograd State Technical University, Volgograd, Russia;b Department of Entomology and Nematology, and Comprehensive Cancer Center, University of California, Davis, CA, USA;c Department of Chemistry, Technology and Equipment of Chemical Industry, Volzhsky Polytechnic Institute (branch) Volgograd State Technical University, Volzhsky, RussiaView further author information

Christophe Morisseaub Department of Entomology and Nematology, and Comprehensive Cancer Center, University of California, Davis, CA, USAView further author information

Dmitry V. Danilova Volgograd State Technical University, Volgograd, RussiaView further author information

Boris P. Gladkikha Volgograd State Technical University, Volgograd, RussiaCorrespondence[email protected]
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Vladimir S. D’yachenkoa Volgograd State Technical University, Volgograd, Russia;b Department of Entomology and Nematology, and Comprehensive Cancer Center, University of California, Davis, CA, USAView further author information

Nikolay A. Zefirovd Department of Chemistry, M. V. Lomonosov Moscow State University, Moscow, RussiaView further author information

Olga N. Zefirovad Department of Chemistry, M. V. Lomonosov Moscow State University, Moscow, RussiaView further author information

Gennady M. Butova Volgograd State Technical University, Volgograd, Russia;c Department of Chemistry, Technology and Equipment of Chemical Industry, Volzhsky Polytechnic Institute (branch) Volgograd State Technical University, Volzhsky, RussiaView further author information

Bruce D. Hammockb Department of Entomology and Nematology, and Comprehensive Cancer Center, University of California, Davis, CA, USAView further author information

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Fluorine and chlorine substituted adamantyl-urea as molecular tools for inhibition of human soluble epoxide hydrolase with picomolar efficacy

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Fluorine and chlorine substituted adamantyl-urea as molecular tools for inhibition of human soluble epoxide hydrolase with picomolar efficacy

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