Spirocyclic compounds, potent CCR1 antagonists von Hossain, Nafizal, Ivanova, Svetlana, Bergare, Jonas, Eriksson, Tomas

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Design, synthesis and structure activity relationships of spirocyclic compounds as potent CCR1 antagonists von Hossain, Nafizal, Ivanova, Svetlana, Bergare, Jonas, Mensonides-Harsema, Marguérite, Cooper, Martin E.

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AZD0284, a Potent, Selective, and Orally Bioavailable Inverse Agonist of Retinoic Acid Receptor-Related Orphan Receptor C2 von Narjes, Frank, Llinas, Antonio, von Berg, Stefan, Jirholt, Johan, Lever, Sarah, Pehrson, Rikard, Collins, Mia, Malmberg, Anna, Svanberg, Petter, Xue, Yafeng, Olsson, Roine I, Malmberg, Jesper, Hughes, Glyn, Hossain, Nafizal, Grindebacke, Hanna, Leffler, Agnes, Krutrök, Nina, Bäck, Elisabeth, Ramnegård, Marie, Lepistö, Matti, Thunberg, Linda, Aagaard, Anna, McPheat, Jane, Hansson, Eva L, Chen, Rongfeng, Xiong, Yao, Hansson, Thomas G

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Potent and Orally Bioavailable Inverse Agonists of RORγt Resulting from Structure-Based Design von Narjes, Frank, Xue, Yafeng, von Berg, Stefan, Malmberg, Jesper, Llinas, Antonio, Olsson, Roine I, Jirholt, Johan, Grindebacke, Hanna, Leffler, Agnes, Hossain, Nafizal, Lepistö, Matti, Thunberg, Linda, Leek, Hanna, Aagaard, Anna, McPheat, Jane, Hansson, Eva L, Bäck, Elisabeth, Tångefjord, Stefan, Chen, Rongfeng, Xiong, Yao, Hongbin, Ge, Hansson, Thomas G

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Selective Nonsteroidal Glucocorticoid Receptor Modulators for the Inhaled Treatment of Pulmonary Diseases von Hemmerling, Martin, Nilsson, Stinabritt, Edman, Karl, Eirefelt, Stefan, Russell, Wayne, Hendrickx, Ramon, Johnsson, Eskil, Kärrman Mårdh, Carina, Berger, Markus, Rehwinkel, Hartmut, Abrahamsson, Anna, Dahmén, Jan, Eriksson, Anders R, Gabos, Balint, Henriksson, Krister, Hossain, Nafizal, Ivanova, Svetlana, Jansson, Anne-Helene, Jensen, Tina J, Jerre, Anders, Johansson, Henrik, Klingstedt, Tomas, Lepistö, Matti, Lindsjö, Martin, Mile, Irene, Nikitidis, Grigorios, Steele, John, Tehler, Ulrika, Wissler, Lisa, Hansson, Thomas

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The synthesis of new 3'-bis-C-substituted-3'-deoxy-3'-dehydro-[3.3.0]-α-fused thymidines by intramolecular radical trapping by tethered acetylenes von GARG, N, HOSSAIN, N, CHATTOPADHYAYA, J

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A novel donor for stereoselective α-sialylation; efficient synthesis of an α(2–8)-linked bis-sialic acid unit von Hossain, Nafizal, Magnusson, Göran

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Synthesis of homo-N-nucleosides, a series of C1' branched-chain nucleosides von Hossain, Nafizal, Blaton, Norbert, Peeters, Oswald, Rozenski, Jef, Herdewijn, Piet A.

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Structure activity relationships of fused bicyclic and urea derivatives of spirocyclic compounds as potent CCR1 antagonists von Hossain, Nafizal, Mensonides-Harsema, Marguérite, Cooper, Martin E, Eriksson, Tomas, Ivanova, Svetlana, Bergström, Lena

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Synthesis of 3′- C-branched 1′,5′-anhydromannitol nucleosides as new antiherpes agents von Hossain, Nafizal, van Halbeek, Herman, De Clercq, Erik, Herdewijn, Piet

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Design, synthesis and structure–activity relationships of zwitterionic spirocyclic compounds as potent CCR1 antagonists von Hossain, Nafizal, Ivanova, Svetlana, Timén, Åsa Sjöholm, Bergare, Jonas, Mussie, Tesfaledet, Bergström, Lena

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New synthesis of 2',3'-dideoxy-2',3'-didehydro-3'-C-substituted thymidines von NAFIZAL HOSSAIN, GARG, N, JYOTI CHATTOPADHYAYA

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Facile Synthesis of 3′-C-Branched 1,5-Anhydrohexitol Nucleosides von Hossain, Nafizal, Herdewijn, Piet

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ChemInform Abstract: Spirocyclic Compounds, Potent CCR1 Antagonists von Hossain, Nafizal, Ivanova, Svetlana, Bergare, Jonas, Eriksson, Tomas

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Corrigendum to “Synthesis of 3′- C-branched 1′,5′-anhydromannitol nucleosides as new antiherpes agents” [Tetrahedron 54 (1998) 2209] von Hossain, Nafizal, van Halbeek, Herman, De Clercq, Erik, Herdewijn, Piet

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Synthesis and antiviral activity of acyclic analogues of 1,5-anhydrohexitol nucleosides using Mitsunobu reaction von Hossain, Nafizal, Rozenski, Jef, De Clercq, Erik, Herdewijn, Piet

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ChemInform Abstract: Design, Synthesis and Structure-Activity Relationships of Zwitterionic Spirocyclic Compounds as Potent CCR1 Antagonists von Hossain, Nafizal, Ivanova, Svetlana, Timen, Aasa Sjoeholm, Bergare, Jonas, Mussie, Tesfaledet, Bergstroem, Lena

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Synthesis and Antiviral Activity of the α-Analogues of 1,5-Anhydrohexitol Nucleosides (1,5-Anhydro-2,3-dideoxy-d-ribohexitol Nucleosides) von Hossain, Nafizal, Rozenski, Jef, De Clercq, Erik, Herdewijn, Piet

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Synthesis and Antiviral Activity of the alpha-Analogues of 1,5-Anhydrohexitol Nucleosides (1,5-Anhydro-2,3-dideoxy-D-ribohexitol Nucleosides) von Hossain, Nafizal, Rozenski, Jef, De Clercq, Erik, Herdewijn, Piet

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Synthesis of homo-N-nucleosides, a series of C1' branched-chain nucleosides von Hossain, Nafizal, Blaton, Norbert, Peeters, Oswald, Rozenski, Jef, Herdewijn, Piet

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