In vivo antitumor activity of NVP-AEW541—A novel, potent, and selective inhibitor of the IGF-IR kinase von Garcı́a-Echeverrı́a, Carlos, Pearson, Mark A, Marti, Andreas, Meyer, Thomas, Mestan, Juergen, Zimmermann, Johann, Gao, Jiaping, Brueggen, Josef, Capraro, Hans-Georg, Cozens, Robert, Evans, Dean B, Fabbro, Doriano, Furet, Pascal, Porta, Diana Graus, Liebetanz, Janis, Martiny-Baron, Georg, Ruetz, Stephan, Hofmann, Francesco

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Pharmacokinetics and Body Distribution of Liposomal Zinc Phthalocyanine in Tumor‐Bearing Mice: Influence of Aggregation State, Particle Size, and Composition von Isele, Ute, Schieweck, Klaus, Kessler, Reinhard, van Hoogevest, Peter, Capraro, Hans‐Georg

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New Aza-Dipeptide Analogues as Potent and Orally Absorbed HIV-1 Protease Inhibitors:  Candidates for Clinical Development von Bold, Guido, Fässler, Alexander, Capraro, Hans-Georg, Cozens, Robert, Klimkait, Thomas, Lazdins, Janis, Mestan, Jürgen, Poncioni, Bernard, Rösel, Johannes, Stover, David, Tintelnot-Blomley, Marina, Acemoglu, Figan, Beck, Werner, Boss, Eugen, Eschbach, Martin, Hürlimann, Thomas, Masso, Elvira, Roussel, Serge, Ucci-Stoll, Katharina, Wyss, Dominique, Lang, Marc

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2,6,9-trisubstituted purines : Optimization towards highly potent and selective CDK1 inhibitors von Imbach, Patricia, Capraro, Hans-Georg, Furet, Pascal, Mett, Helmut, Meyer, Thomas, Zimmermann, Jürg

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Large‐Scale Production of Liposomes Containing Monomeric Zinc Phthalocyanine by Controlled Dilution of Organic Solvents von Isele, Ute, Van Hoogevest, Peter, Hilfiker, Rolf, Capraro, Hans‐Georg, Schieweck, Klaus, Leuenberger, Hans

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Aza-Peptide Analogs as Potent Human Immunodeficiency Virus Type-1 Protease Inhibitors with Oral Bioavailability von Fässler, Alexander, Bold, Guido, Capraro, Hans-Georg, Cozens, Robert, Mestan, Jürgen, Poncioni, Bernard, Rösel, Johannes, Tintelnot-Blomley, Marina, Lang, Marc

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Structure-based design of potent CDK1 inhibitors derived from olomoucine von Furet, P, Zimmermann, J, Capraro, H G, Meyer, T, Imbach, P

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Synthesis of Potent and Orally Active HIV-Protease Inhibitors von Capraro, Hans-Georg, Bold, Guido, Fässler, Alexander, Cozens, Robert, Klimkait, Thomas, Lazdins, Janis, Mestan, Jürgen, Poncioni, Bernard, Rösel, Johannes L., Stover, David, Lang, Marc

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Biological effects of modified colchicines. Improved preparation of 2-demethylcolchicine, 3-demethylcolchicine, and (+)-colchicine and reassignment of the position of the double bo... von Roesner, Manfred, Capraro, Hans-Georg, Jacobson, Arthur E, Atwell, Louise, Brossi, Arnold, Iorio, Maria A, Williams, Thomas H, Sik, Robert H, Chignell, Colin F

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Simple Conversion of Colchicine into Demecolcine von Capraro, Hans-Georg, Brossi, Arnold

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Twista-4,9-diene. Preliminary communication von Capraro, Hans-Georg, Ganter, Camille

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The Novel Adamantane Isomer 2,5-Trimethylenenorbornane (Tricycio-[5.3.0.3,9]decane, 4-Homotwistbrendane) von Känel, Hans-Ruedi, Capraro, Hans-Georg, Ganter, Camille

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In vitro Effect of$\alpha_{1}$-Acid Glycoprotein on the Anti-Human Immunodeficiency Virus (HIV) Activity of the Protease Inhibitor CGP 61755: A Comparative Study with Other Relevan... von Lazdins, Janis K., Mestan, Jürgen, Goutte, Gerard, Walker, Maja R., Bold, Guido, Capraro, Hans Georg, Klimkait, Thomas

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SYNTHESIS AND BIOLOGICAL ACTIVITY OF 2-LACTONYL PENEMS von CAPRARO, HANS-GEORG, FRANCOTTE, ERIC, KOHLER, BORIS, RIHS, GRETHY, SCHNEIDER, PETER, SCARTAZZINI, RICCARDO, ZAK, OTO, TOSCH, WERNER

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imidazopiridazinas como inibidores de pi3k lipídeo cinase von Hans-Georg Capraro, Patricia Imbach, Giorgio Caravatti, Pascal Furet

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ChemInform Abstract: 2,6,9-Trisubstituted Purines: Optimization Towards Highly Potent and Selective CDK1 Inhibitors von Imbach, Patricia, Capraro, Hans-Georg, Furet, Pascal, Mett, Helmut, Meyer, Thomas, Zimmermann, Juerg

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S-Adenosylmethionine decarboxylase inhibitors: new aryl and heteroaryl analogs of methylglyoxal bis(guanylhydrazone) von Stanek, Jaroslav, Caravatti, Giorgio, Capraro, Hans Georg, Furet, Pascal, Mett, Helmut, Schneider, Peter, Regenass, Urs

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Corrigendum to “2,6,9-trisubstituted purines: optimization towards highly potent and selective CDK1 inhibitors” von Imbach, Patricia, Capraro, Hans-Georg, Furet, Pascal, Mett, Helmut, Meyer, Thomas, Zimmermann, Jürg

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13C- and 1H-NMR. Assignments for colchicine derivatives von Hufford, Charles D., Capraro, Hans-Georg, Brossi, Arnold

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LU91189I von LANG Marc, BOLD Guido, FÄSSLER Alexander, CAPRARO Hans-Georg, KHANNA Satish, Chandra

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