Search Results - "Bodensieck, Antje"

New Eremophilane Sesquiterpenes from a Rhizome Extract of Petasites hybridus by Bodensieck, Antje, Kunert, Olaf, Haslinger, Ernst, Bauer, Rudolf

“…A total of 21 natural products, 1–21, were isolated from a supercritical CO2 extract of the rhizomes of Petasites hybridus. Thereby, seven new eremophilane (=…”
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Absolute configuration of eremophilane sesquiterpenes from Petasites hybridus: Comparison of experimental and calculated circular dichroism spectra by Bodensieck, Antje, Fabian, Walter M.F., Kunert, Olaf, Belaj, Ferdinand, Jahangir, Sajid, Schühly, Wolfgang, Bauer, Rudolf

“…In‐depth conformational analyses of 10 known eremophilane (= (1S,4aR,7R,8aR)‐decahydro‐1,8a‐dimethyl‐7‐(1‐methylethyl)napththalene) sesquiterpenes, 1–10, from…”
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Lignan Derivatives from Krameria lappacea Roots Inhibit Acute Inflammation in Vivo and Pro-inflammatory Mediators in Vitro by Baumgartner, Lisa, Sosa, Silvio, Atanasov, Atanas G, Bodensieck, Antje, Fakhrudin, Nanang, Bauer, Julia, Favero, Giorgia Del, Ponti, Cristina, Heiss, Elke H, Schwaiger, Stefan, Ladurner, Angela, Widowitz, Ute, Loggia, Roberto Della, Rollinger, Judith M, Werz, Oliver, Bauer, Rudolf, Dirsch, Verena M, Tubaro, Aurelia, Stuppner, Hermann

“…The roots of Krameria lappacea are used traditionally against oropharyngeal inflammation. So far, the astringent and antimicrobial properties of its…”
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Differential and stereoselective in vitro cytotoxicity of eremophilane sesquiterpenes of Petasites hybridus rhizomes in rat hepatocytes by Bodensieck, Antje, Gaunitz, Frank, Gebhardt, Rolf, Danesch, Ulrich, Bauer, Rudolf

“…We tested two CO (2) extracts of Petasites hybridus L. rhizomes, A (rich in furanoeremophilanes) and B (rich in petasins), for IN VITRO cytotoxicity in rat…”
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Design and synthesis of ten biphenyl-neolignan derivatives and their in vitro inhibitory potency against cyclooxygenase-1/2 activity and 5-lipoxygenase-mediated LTB4-formation by SCHÜHLY, Wolfgang, HÜFNER, Antje, PFERSCHY-WENZIG, Eva M, PRETTNER, Elke, ADAMS, Michael, BODENSIECK, Antje, KUNERT, Olaf, OLUWEMIMO, Asije, HASLINGER, Ernst, BAUER, Rudolf

“…A set of ten derivatives of methylhonokiol, an anti-inflammatory active biphenyl-type neolignan from Magnolia grandiflora, has been evaluated for their in…”
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Design and synthesis of ten biphenyl-neolignan derivatives and their in vitro inhibitory potency against cyclooxygenase-1/2 activity and 5-lipoxygenase-mediated LTB sub(4)-formation by Schuehly, Wolfgang, Huefner, Antje, Pferschy-Wenzig, Eva M, Prettner, Elke, Adams, Michael, Bodensieck, Antje, Kunert, Olaf, Oluwemimo, Asije, Haslinger, Ernst, Bauer, Rudolf

“…A set of ten derivatives of methylhonokiol, an anti-inflammatory active biphenyl-type neolignan from Magnolia grandiflora, has been evaluated for their in…”
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Discovering COX-inhibiting constituents of Morus root bark: activity-guided versus computer-aided methods by Rollinger, Judith M, Bodensieck, Antje, Seger, Christoph, Ellmerer, Ernst P, Bauer, Rudolf, Langer, Thierry, Stuppner, Hermann

“…The aim of this study was to compare the efficiency of two well known approaches for the discovery of the bioactive principle/s in medicinal plants, namely the…”
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Synthesis and biological evaluation of a new class of acyl derivatives of 3-amino-1-phenyl-4,5-dihydro-1H-pyrazol-5-one as potential dual cyclooxygenase (COX-1 and COX-2) and human lipoxygenase (5-LOX) inhibitors by Cusan, Claudia, Spalluto, Giampiero, Prato, Maurizio, Adams, Michael, Bodensieck, Antje, Bauer, Rudolf, Tubaro, Aurelia, Bernardi, Paolo, Da Ros, Tatiana

“…A series of acyl derivatives of 3-amino-1-phenyl-4,5-dihydro-1H-pyrazol-5-one as potential human 5-LOX and COX 1 and COX-2 inhibitors structurally related to…”
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Synthesis and biological evaluation of new phenidone analogues as potential dual cyclooxygenase (COX-1 and COX-2) and human lipoxygenase (5-LOX) inhibitors by Cusan, Claudia, Spalluto, Giampiero, Prato, Maurizio, Adams, Michael, Bodensieck, Antje, Bauer, Rudolf, Tubaro, Aurelia, Bernardi, Paolo, Da Ros, Tatiana

“…A new series of potential human 5-LOX inhibitors structurally related to the 1-phenyl-3-pyrazolidinone (phenidone, 2) has been synthesized and the activity…”
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Synthesis and biological evaluation of a new class of acyl derivatives of 3-amino-1-phenyl-4,5-dihydro-1 H-pyrazol-5-one as potential dual cyclooxygenase (COX-1 and COX-2) and human lipoxygenase (5-LOX) inhibitors by Cusan, Claudia, Spalluto, Giampiero, Prato, Maurizio, Adams, Michael, Bodensieck, Antje, Bauer, Rudolf, Tubaro, Aurelia, Bernardi, Paolo, Da Ros, Tatiana

“…A series of acyl derivatives of 3-amino-1-phenyl-4,5-dihydro-1 H-pyrazol-5-one as potential human 5-LOX and COX 1 and COX-2 inhibitors structurally related to…”
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