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H G Capraro

Showing results (1-10 of 14) with videos related to

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The Journal of Biological Chemistry|August 10, 1980
Colchicine binding to antibodiesJ Wolff, H G Capraro, A Brossi, et al.
Journal of Computer-Aided Molecular Design|July 15, 2000
Structure-based design of potent CDK1 inhibitors derived from olomoucineP Furet, J Zimmermann, H G Capraro, et al.
Journal of Pharmaceutical Sciences|February 1, 1995
Pharmacokinetics and body distribution of liposomal zinc phthalocyanine in tumor-bearing mice: influence of aggregation state, particle size, and compositionU Isele, K Schieweck, R Kessler, et al.
Bioorganic & Medicinal Chemistry Letters|February 17, 1999
2,6,9-trisubstituted purines: optimization towards highly potent and selective CDK1 inhibitorsP Imbach, H G Capraro, P Furet, et al.
British Journal of Cancer|May 1, 1994
CGP 55398, a liposomal Ge(IV) phthalocyanine bearing two axially ligated cholesterol moieties: a new potential agent for photodynamic therapy of tumoursA Segalla, C Milanesi, G Jori, et al.
Journal of Pharmaceutical Sciences|November 1, 1994
Large-scale production of liposomes containing monomeric zinc phthalocyanine by controlled dilution of organic solventsU Isele, P van Hoogevest, R Hilfiker, et al.
Journal of Medicinal Chemistry|January 8, 1993
S-adenosylmethionine decarboxylase inhibitors: new aryl and heteroaryl analogues of methylglyoxal bis(guanylhydrazone)J Stanek, G Caravatti, H G Capraro, et al.
The Journal of Antibiotics|June 1, 1988
Synthesis and biological activity of 2-lactonyl penemsH G Capraro, E Francotte, B Kohler, et al.
The Journal of Infectious Diseases|May 1, 1997
In vitro effect of alpha1-acid glycoprotein on the anti-human immunodeficiency virus (HIV) activity of the protease inhibitor CGP 61755: a comparative study with other relevant HIV protease inhibitorsJ K Lazdins, J Mestan, G Goutte, et al.
Journal of Medicinal Chemistry|August 2, 1996
Aza-peptide analogs as potent human immunodeficiency virus type-1 protease inhibitors with oral bioavailabilityA Fässler, G Bold, H G Capraro, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
The Journal of Biological Chemistry|August 10, 1980
Colchicine binding to antibodiesJ Wolff, H G Capraro, A Brossi, et al.
Journal of Computer-Aided Molecular Design|July 15, 2000
Structure-based design of potent CDK1 inhibitors derived from olomoucineP Furet, J Zimmermann, H G Capraro, et al.
Journal of Pharmaceutical Sciences|February 1, 1995
Pharmacokinetics and body distribution of liposomal zinc phthalocyanine in tumor-bearing mice: influence of aggregation state, particle size, and compositionU Isele, K Schieweck, R Kessler, et al.
Bioorganic & Medicinal Chemistry Letters|February 17, 1999
2,6,9-trisubstituted purines: optimization towards highly potent and selective CDK1 inhibitorsP Imbach, H G Capraro, P Furet, et al.
British Journal of Cancer|May 1, 1994
CGP 55398, a liposomal Ge(IV) phthalocyanine bearing two axially ligated cholesterol moieties: a new potential agent for photodynamic therapy of tumoursA Segalla, C Milanesi, G Jori, et al.
Journal of Pharmaceutical Sciences|November 1, 1994
Large-scale production of liposomes containing monomeric zinc phthalocyanine by controlled dilution of organic solventsU Isele, P van Hoogevest, R Hilfiker, et al.
Journal of Medicinal Chemistry|January 8, 1993
S-adenosylmethionine decarboxylase inhibitors: new aryl and heteroaryl analogues of methylglyoxal bis(guanylhydrazone)J Stanek, G Caravatti, H G Capraro, et al.
The Journal of Antibiotics|June 1, 1988
Synthesis and biological activity of 2-lactonyl penemsH G Capraro, E Francotte, B Kohler, et al.
The Journal of Infectious Diseases|May 1, 1997
In vitro effect of alpha1-acid glycoprotein on the anti-human immunodeficiency virus (HIV) activity of the protease inhibitor CGP 61755: a comparative study with other relevant HIV protease inhibitorsJ K Lazdins, J Mestan, G Goutte, et al.
Journal of Medicinal Chemistry|August 2, 1996
Aza-peptide analogs as potent human immunodeficiency virus type-1 protease inhibitors with oral bioavailabilityA Fässler, G Bold, H G Capraro, et al.
Pageof 2