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The Journal of Biological Chemistry
|
August 10, 1980
Colchicine binding to antibodies
J 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 olomoucine
P 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 composition
U 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 inhibitors
P 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 tumours
A 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 solvents
U 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 penems
H 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 inhibitors
J 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 bioavailability
A Fässler, G Bold, H G Capraro, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
The Journal of Biological Chemistry
|
August 10, 1980
Colchicine binding to antibodies
J 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 olomoucine
P 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 composition
U 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 inhibitors
P 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 tumours
A 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 solvents
U 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 penems
H 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 inhibitors
J 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 bioavailability
A Fässler, G Bold, H G Capraro, et al.
Page
of 2