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Lukasz Berlicki

Showing results (1-10 of 10) with videos related to

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Bioorganic & Medicinal Chemistry|March 1, 2006
Computer-aided analysis of the interactions of glutamine synthetase with its inhibitorsLukasz Berlicki, Paweł Kafarski
Chirality|March 24, 2009
Enantiodifferentiation of alpha-hydroxyalkanephosphonic acids in 31P NMR with application of alpha-cyclodextrin as chiral discriminating agentEwa Rudzińska, Gabriela Dziedzioła, Lukasz Berlicki, et al.
Journal of Agricultural and Food Chemistry|May 4, 2007
Plant P5C reductase as a new target for aminomethylenebisphosphonatesGiuseppe Forlani, Samuele Giberti, Lukasz Berlicki, et al.
Journal of Medicinal Chemistry|August 6, 2010
Computer-aided optimization of phosphinic inhibitors of bacterial ureasesStamatia Vassiliou, Paulina Kosikowska, Agnieszka Grabowiecka, et al.
Journal of Agricultural and Food Chemistry|May 27, 2004
Herbicidal pyridyl derivatives of aminomethylene-bisphosphonic acid inhibit plant glutamine synthetaseAgnieszka Obojska, Lukasz Berlicki, Paweł Kafarski, et al.
Amino Acids|May 12, 2011
N-substituted aminomethanephosphonic and aminomethane-P-methylphosphinic acids as inhibitors of ureasesLukasz Berlicki, Marta Bochno, Agnieszka Grabowiecka, et al.
Journal of Agricultural and Food Chemistry|April 11, 2008
Tailoring the structure of aminobisphosphonates to target plant P5C reductaseGiuseppe Forlani, Andrea Occhipinti, Lukasz Berlicki, et al.
Journal of Agricultural and Food Chemistry|June 25, 2013
Synthesis and evaluation of effective inhibitors of plant δ1-pyrroline-5-carboxylate reductaseGiuseppe Forlani, Lukasz Berlicki, Mattia Duò, et al.
Amino Acids|July 12, 2011
Δ1-pyrroline-5-carboxylate reductase as a new target for therapeutics: inhibition of the enzyme from Streptococcus pyogenes and effects in vivoGiuseppe Forlani, Davide Petrollino, Massimo Fusetti, et al.
Journal of Medicinal Chemistry|October 5, 2013
Replacement of Thr32 and Gln34 in the C-terminal neuropeptide Y fragment 25-36 by cis-cyclobutane and cis-cyclopentane β-amino acids shifts selectivity toward the Y(4) receptorLukasz Berlicki, Melanie Kaske, Raquel Gutiérrez-Abad, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Bioorganic & Medicinal Chemistry|March 1, 2006
Computer-aided analysis of the interactions of glutamine synthetase with its inhibitorsLukasz Berlicki, Paweł Kafarski
Chirality|March 24, 2009
Enantiodifferentiation of alpha-hydroxyalkanephosphonic acids in 31P NMR with application of alpha-cyclodextrin as chiral discriminating agentEwa Rudzińska, Gabriela Dziedzioła, Lukasz Berlicki, et al.
Journal of Agricultural and Food Chemistry|May 4, 2007
Plant P5C reductase as a new target for aminomethylenebisphosphonatesGiuseppe Forlani, Samuele Giberti, Lukasz Berlicki, et al.
Journal of Medicinal Chemistry|August 6, 2010
Computer-aided optimization of phosphinic inhibitors of bacterial ureasesStamatia Vassiliou, Paulina Kosikowska, Agnieszka Grabowiecka, et al.
Journal of Agricultural and Food Chemistry|May 27, 2004
Herbicidal pyridyl derivatives of aminomethylene-bisphosphonic acid inhibit plant glutamine synthetaseAgnieszka Obojska, Lukasz Berlicki, Paweł Kafarski, et al.
Amino Acids|May 12, 2011
N-substituted aminomethanephosphonic and aminomethane-P-methylphosphinic acids as inhibitors of ureasesLukasz Berlicki, Marta Bochno, Agnieszka Grabowiecka, et al.
Journal of Agricultural and Food Chemistry|April 11, 2008
Tailoring the structure of aminobisphosphonates to target plant P5C reductaseGiuseppe Forlani, Andrea Occhipinti, Lukasz Berlicki, et al.
Journal of Agricultural and Food Chemistry|June 25, 2013
Synthesis and evaluation of effective inhibitors of plant δ1-pyrroline-5-carboxylate reductaseGiuseppe Forlani, Lukasz Berlicki, Mattia Duò, et al.
Amino Acids|July 12, 2011
Δ1-pyrroline-5-carboxylate reductase as a new target for therapeutics: inhibition of the enzyme from Streptococcus pyogenes and effects in vivoGiuseppe Forlani, Davide Petrollino, Massimo Fusetti, et al.
Journal of Medicinal Chemistry|October 5, 2013
Replacement of Thr32 and Gln34 in the C-terminal neuropeptide Y fragment 25-36 by cis-cyclobutane and cis-cyclopentane β-amino acids shifts selectivity toward the Y(4) receptorLukasz Berlicki, Melanie Kaske, Raquel Gutiérrez-Abad, et al.
Pageof 1