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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext bestellen

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

Volltext

(+)-(1S, 3S, 6S, 8S)-und (−)-(1R, 3R, 6R, 8R)-4, 9-Twistadien: Synthese und Bestimmung der absoluten Konfiguration von Capraro, Hans-Georg, Ganter, Camille

Volltext

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

Volltext