Discovery of aryl ureas and aryl amides as potent and selective histamine H-3 receptor antagonists for the treatment of obesity (Part I)
Gao, Zhongli, Hurst, William J., Guillot, Etienne, Czechtizky, Werngard, Lukasczyk, Ulrike, Nagorny, Raisa, Pruniaux, Marie-Pierre, Schwink, Lothar, Sanchez, Juan Antonio, Stengelin, Siegfried, Tang, Lei, Winkler, Irvin, Hendrix, James A., George, Pascal G.
Published in Bioorganic & medicinal chemistry letters (01.06.2013)
Published in Bioorganic & medicinal chemistry letters (01.06.2013)
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Discovery of aryl ureas and aryl amides as potent and selective histamine H-3 receptor antagonists for the treatment of obesity (Part II)
Gao, Zhongli, Hurst, William J., Guillot, Etienne, Czechtizky, Werngard, Lukasczyk, Ulrike, Nagorny, Raisa, Pruniaux, Marie-Pierre, Schwink, Lothar, Sanchez, Juan Antonio, Stengelin, Siegfried, Tang, Lei, Winkler, Irvin, Hendrix, James A., George, Pascal G.
Published in Bioorganic & medicinal chemistry letters (01.06.2013)
Published in Bioorganic & medicinal chemistry letters (01.06.2013)
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Journal Article
Discovery of aryl ureas and aryl amides as potent and selective histamine H3 receptor antagonists for the treatment of obesity (Part I)
Gao, Zhongli, Hurst, William J., Guillot, Etienne, Czechtizky, Werngard, Lukasczyk, Ulrike, Nagorny, Raisa, Pruniaux, Marie-Pierre, Schwink, Lothar, Sanchez, Juan Antonio, Stengelin, Siegfried, Tang, Lei, Winkler, Irvin, Hendrix, James A., George, Pascal G.
Published in Bioorganic & medicinal chemistry letters (01.06.2013)
Published in Bioorganic & medicinal chemistry letters (01.06.2013)
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Journal Article
Discovery of aryl ureas and aryl amides as potent and selective histamine H3 receptor antagonists for the treatment of obesity (Part II)
Gao, Zhongli, Hurst, William J., Guillot, Etienne, Czechtizky, Werngard, Lukasczyk, Ulrike, Nagorny, Raisa, Pruniaux, Marie-Pierre, Schwink, Lothar, Sanchez, Juan Antonio, Stengelin, Siegfried, Tang, Lei, Winkler, Irvin, Hendrix, James A., George, Pascal G.
Published in Bioorganic & medicinal chemistry letters (01.06.2013)
Published in Bioorganic & medicinal chemistry letters (01.06.2013)
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Structures of Tyr188Leu mutant and wild-type HIV-1 reverse transcriptase complexed with the non-nucleoside inhibitor HBY 097: inhibitor flexibility is a useful design feature for reducing drug resistance
Hsiou, Y, Das, K, Ding, J, Clark, Jr, A D, Kleim, J P, Rösner, M, Winkler, I, Riess, G, Hughes, S H, Arnold, E
Published in Journal of molecular biology (27.11.1998)
Published in Journal of molecular biology (27.11.1998)
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CEFODIZIME, AN AMINOTHIAZOLYL CEPHALOSPORIN: IV. INFLUENCE ON THE IMMUNE SYSTEM
LIMBERT, MICHAEL, BARTLETT, ROBERT R., DICKNEITE, GERHARD, KLESEL, NORBERT, SCHORLEMMER, HANS ULRICH, SEIBERT, GERHARD, WINKLER, IRVIN, SCHRINNER, ELMAR
Published in Journal of antibiotics (1984)
Published in Journal of antibiotics (1984)
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ANTIBACTERIAL AND ANTIVIRAL PEPTIDES FROM ACTINOMADURA NAMIBIENSIS
WINKLER IRVIN, BROENSTRUP MARK, SEIBERT GERHARD, SHELDRICK GEORGE M, SUSSMUTH RODERICH, MEINDL KATHRIN, GUEHRING HANS, WINK JOACHIM, TOTI LUIGI, VERTESY LASZLO, HOFFMANN HOLGER
Year of Publication 08.07.2009
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Year of Publication 08.07.2009
Patent
Selective Pressure of a Quinoxaline Nonnucleoside Inhibitor of Human Immunodeficiency Virus Type 1 (HIV-1) Reverse Transcriptase (RT) on HIV-1 Replication Results in the Emergence of Nucleoside RT-Inhibitor-Specific (RT Leu-74 → Val or Ile and Val-75 → Leu or Ile) HIV-1 mutants
Kleim, Jörg-Peter, Rösner, Manfred, Winkler, Irvin, Paessens, Arno, Kirsch, Reinhard, Hsiou, Yu, Arnold, Edward, Riess, Günther
Published in Proceedings of the National Academy of Sciences - PNAS (09.01.1996)
Published in Proceedings of the National Academy of Sciences - PNAS (09.01.1996)
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In vitro selection for different mutational patterns in the HIV-1 reverse transcriptase using high and low selective pressure of the nonnucleoside reverse transcriptase inhibitor HBY 097
Kleim, J P, Winkler, I, Rösner, M, Kirsch, R, Rübsamen-Waigmann, H, Paessens, A, Riess, G
Published in Virology (New York, N.Y.) (28.04.1997)
Published in Virology (New York, N.Y.) (28.04.1997)
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Selective pressure of a quinoxaline nonnucleoside inhibitor of human immunodeficiency virus type 1 (HIV-1) reverse transcriptase (RT) on HIV-1 replication results in the emergence of nucleoside RT-inhibitor-specific (RT Leu-74 gives Val or Ile
Kleim, Jorg-Peter, Rosner, Manfred, Winkler, Irvin, Paessens, Arno
Published in Proceedings of the National Academy of Sciences - PNAS (09.01.1996)
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Published in Proceedings of the National Academy of Sciences - PNAS (09.01.1996)
Journal Article
Antiviral Activity of the Human Immunodeficiency Virus Type 1—Specific Nonnucleoside Reverse Transcriptase Inhibitor HBY 097 Alone and in Combination with Zidovudine in a Phase II Study
Kleim, Jörg-Peter, Winters, Mark, Dunkler, Anke, Suarez, José-Ramon, Rieß, Günther, Winkler, Irvin, Balzarini, Jan, Oette, Dagmar, Merigan, Thomas C.
Published in The Journal of infectious diseases (01.03.1999)
Published in The Journal of infectious diseases (01.03.1999)
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In VitroSelection for Different Mutational Patterns in the HIV-1 Reverse Transcriptase Using High and Low Selective Pressure of the Nonnucleoside Reverse Transcriptase Inhibitor HBY 097
Kleim, Jörg-Peter, Winkler, Irvin, Rösner, Manfred, Kirsch, Reinhard, Rübsamen-Waigmann, Helga, Paessens, Arno, Riess, Günther
Published in Virology (New York, N.Y.) (28.04.1997)
Published in Virology (New York, N.Y.) (28.04.1997)
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Structures of Tyr188Leu mutant and wild-type HIV-1 reverse transcriptase complexed with the non-nucleoside inhibitor HBY 097: inhibitor flexibility is a useful design feature for reducing drug resistance 1 1Edited by J. Karn
Hsiou, Yu, Das, Kalyan, Ding, Jianping, Clark, Arthur D., Kleim, Jörg-Peter, Rösner, Manfred, Winkler, Irvin, Riess, Günther, Hughes, Stephen H., Arnold, Edward
Published in Journal of molecular biology (01.11.1998)
Published in Journal of molecular biology (01.11.1998)
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Journal Article
Retention of marked sensitivity to ( S)-4-isopropoxycarbonyl-6-methoxy-3-(methylthiomethyl)-3,4-Dihydroquinoxaline-2(1H)-Thione (HBY 097) by an azidothymidine (AZT)-resistant human immunodeficiency virus type 1 (HIV-1) strain subcultured in the combined presence of quinoxaline HBY 097 and 2′,3′-dideoxy-3′-thiacytidine (Lamivudine)
Balzarini, Jan, Pelemans, Heidi, Riess, Gunther, Roesner, Manfred, Winkler, Irvin, De Ckrcq, Erik, Kleim, Jörg-Peter
Published in Biochemical pharmacology (01.03.1998)
Published in Biochemical pharmacology (01.03.1998)
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