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Ralph Holl

Showing results (11-20 of 28) with videos related to

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Organic & Biomolecular Chemistry|August 7, 2013
Synthesis and biological evaluation of flexible and conformationally constrained LpxC inhibitorsMarius Löppenberg, Hannes Müller, Carla Pulina, et al.
Frontiers in Chemistry|May 14, 2023
Editorial: Emerging heterocycles as bioactive compoundsGiovanna Li Petri, Ralph Holl, Virginia Spanò, et al.
Bioorganic & Medicinal Chemistry|February 1, 2016
Synthesis and biological evaluation of enantiomerically pure glyceric acid derivatives as LpxC inhibitorsGiovanni Tangherlini, Tullio Torregrossa, Oriana Agoglitta, et al.
Topics in Current Chemistry (Cham)|August 10, 2021
Pyrrolidine in Drug Discovery: A Versatile Scaffold for Novel Biologically Active CompoundsGiovanna Li Petri, Maria Valeria Raimondi, Virginia Spanò, et al.
Chemmedchem|February 26, 2019
Chiral Pool Synthesis, Biological Evaluation and Molecular Docking Studies of C-Furanosidic LpxC InhibitorsAlexander Dreger, Omar Kharwb, Oriana Agoglitta, et al.
Bioorganic Chemistry|November 10, 2021
Synthesis, biological evaluation, and molecular docking studies of deoxygenated C-glycosides as LpxC inhibitorsAlexander Dreger, Katharina Hoff, Oriana Agoglitta, et al.
European Journal of Medicinal Chemistry|September 11, 2020
Bioactive pyrrole-based compounds with target selectivityGiovanna Li Petri, Virginia Spanò, Roberto Spatola, et al.
Bioorganic Chemistry|January 11, 2021
Antibacterial activity of xylose-derived LpxC inhibitors - Synthesis, biological evaluation and molecular docking studiesAlexander Dreger, Katharina Hoff, Oriana Agoglitta, et al.
Chemmedchem|October 15, 2009
Synthesis and pharmacological evaluation of SNC80 analogues with a bridged piperazine ringRalph Holl, Bettina Jung, Dirk Schepmann, et al.
Archiv Der Pharmazie|July 8, 2026
Synthesis, Biological Evaluation, and Molecular Docking Studies of 2r,3t,4c-Configured C-Furanosidic LpxC InhibitorsAndré Behnk, Fabian Lüttchens, Frederick Wichter, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
Organic & Biomolecular Chemistry|August 7, 2013
Synthesis and biological evaluation of flexible and conformationally constrained LpxC inhibitorsMarius Löppenberg, Hannes Müller, Carla Pulina, et al.
Frontiers in Chemistry|May 14, 2023
Editorial: Emerging heterocycles as bioactive compoundsGiovanna Li Petri, Ralph Holl, Virginia Spanò, et al.
Bioorganic & Medicinal Chemistry|February 1, 2016
Synthesis and biological evaluation of enantiomerically pure glyceric acid derivatives as LpxC inhibitorsGiovanni Tangherlini, Tullio Torregrossa, Oriana Agoglitta, et al.
Topics in Current Chemistry (Cham)|August 10, 2021
Pyrrolidine in Drug Discovery: A Versatile Scaffold for Novel Biologically Active CompoundsGiovanna Li Petri, Maria Valeria Raimondi, Virginia Spanò, et al.
Chemmedchem|February 26, 2019
Chiral Pool Synthesis, Biological Evaluation and Molecular Docking Studies of C-Furanosidic LpxC InhibitorsAlexander Dreger, Omar Kharwb, Oriana Agoglitta, et al.
Bioorganic Chemistry|November 10, 2021
Synthesis, biological evaluation, and molecular docking studies of deoxygenated C-glycosides as LpxC inhibitorsAlexander Dreger, Katharina Hoff, Oriana Agoglitta, et al.
European Journal of Medicinal Chemistry|September 11, 2020
Bioactive pyrrole-based compounds with target selectivityGiovanna Li Petri, Virginia Spanò, Roberto Spatola, et al.
Bioorganic Chemistry|January 11, 2021
Antibacterial activity of xylose-derived LpxC inhibitors - Synthesis, biological evaluation and molecular docking studiesAlexander Dreger, Katharina Hoff, Oriana Agoglitta, et al.
Chemmedchem|October 15, 2009
Synthesis and pharmacological evaluation of SNC80 analogues with a bridged piperazine ringRalph Holl, Bettina Jung, Dirk Schepmann, et al.
Archiv Der Pharmazie|July 8, 2026
Synthesis, Biological Evaluation, and Molecular Docking Studies of 2r,3t,4c-Configured C-Furanosidic LpxC InhibitorsAndré Behnk, Fabian Lüttchens, Frederick Wichter, et al.
Pageof 3