UB Paderborn / Katalog / Suche / in CDI

In vivo antitumor activity of NVP-AEW541—A novel, potent, and selective inhibitor of the IGF-IR kinase

Cancer cell, 2004-03, Vol.5 (3), p.231-239

2004

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Pharmacokinetics and Body Distribution of Liposomal Zinc Phthalocyanine in Tumor‐Bearing Mice: Influence of Aggregation State, Particle Size, and Composition

Journal of pharmaceutical sciences, 1995-02, Vol.84 (2), p.166-173

1995

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New Aza-Dipeptide Analogues as Potent and Orally Absorbed HIV-1 Protease Inhibitors: Candidates for Clinical Development

Journal of medicinal chemistry, 1998-08, Vol.41 (18), p.3387-3401

1998

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2,6,9-trisubstituted purines : Optimization towards highly potent and selective CDK1 inhibitors

Bioorganic & medicinal chemistry letters, 1999-01, Vol.9 (1), p.91-96

1999

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Large‐Scale Production of Liposomes Containing Monomeric Zinc Phthalocyanine by Controlled Dilution of Organic Solvents

Journal of pharmaceutical sciences, 1994-11, Vol.83 (11), p.1608-1616

1994

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Aza-Peptide Analogs as Potent Human Immunodeficiency Virus Type-1 Protease Inhibitors with Oral Bioavailability

Journal of medicinal chemistry, 1996-08, Vol.39 (16), p.3203-3216

1996

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Structure-based design of potent CDK1 inhibitors derived from olomoucine

Journal of computer-aided molecular design, 2000-07, Vol.14 (5), p.403-409

2000

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Synthesis of Potent and Orally Active HIV-Protease Inhibitors

Archiv der Pharmazie (Weinheim), 1996-06, Vol.329 (6), p.273-278

1996

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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 bond in dehydro-7-deacetamidocolchicines

Journal of medicinal chemistry, 1981-03, Vol.24 (3), p.257-261

1981

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Simple Conversion of Colchicine into Demecolcine

Helvetica chimica acta, 1979-06, Vol.62 (4), p.965-970

1979

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(+)-(1S, 3S, 6S, 8S)-und (−)-(1R, 3R, 6R, 8R)-4, 9-Twistadien: Synthese und Bestimmung der absoluten Konfiguration

Helvetica chimica acta, 1980-07, Vol.63 (5), p.1347-1351

1980

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[2+2]-Cycloaddition von Ketenen an «Maleinisoimide» und Überführung der spiroverknüpften b̃-Laktame in Muconsäure- und Tetramsäurederivate

Helvetica chimica acta, 1983-02, Vol.66 (1), p.362-378

1983

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Cycloaddition von Chlorsulfonyliscyanat an «Maleinisoimide

Helvetica chimica acta, 1983-03, Vol.66 (2), p.633-638

1983

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Twista-4,9-diene. Preliminary communication

Helvetica chimica acta, 1976, Vol.59 (1), p.97-100

1976

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The Novel Adamantane Isomer 2,5-Trimethylenenorbornane (Tricycio-[5.3.0.3,9]decane, 4-Homotwistbrendane)

Helvetica chimica acta, 1982-05, Vol.65 (3), p.1032-1037

1982

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Synthesis of regiospecifically substituted pyrimidyl derivatives and their incorporation into penems

Heterocycles, 1989, Vol.28 (2), p.643-652

1989

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SYNTHESIS AND BIOLOGICAL ACTIVITY OF 2-LACTONYL PENEMS

The Journal of Antibiotics, 1988/06/25, Vol.41(6), pp.759-770

1988

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ChemInform Abstract: 2,6,9-Trisubstituted Purines: Optimization Towards Highly Potent and Selective CDK1 Inhibitors

ChemInform, 1999-05, Vol.30 (19), p.no-no

1999

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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 Relevant HIV Protease Inhibitors

The Journal of infectious diseases, 1997-05, Vol.175 (5), p.1063-1070

1997

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13C- and 1H-NMR. Assignments for colchicine derivatives

Helvetica chimica acta, 1980-01, Vol.63 (1), p.50-56

1980

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S-Adenosylmethionine decarboxylase inhibitors: new aryl and heteroaryl analogs of methylglyoxal bis(guanylhydrazone)

Journal of medicinal chemistry, 1993, Vol.36 (1), p.46-54

1993

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Corrigendum to “2,6,9-trisubstituted purines: optimization towards highly potent and selective CDK1 inhibitors”

Bioorganic & medicinal chemistry letters, 2000-05, Vol.10 (9), p.1001

2000

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In Vitro Effect of α 1 ‐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

The Journal of infectious diseases, 1997-05, Vol.175 (5), p.1063-1070

1997

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In Vitro Effect of α1-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

The Journal of infectious diseases, 1997-05, Vol.175 (5), p.1063-1070

1997

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(+)‐(1S, 3S, 6S, 8S)‐und (−)‐(1R, 3R, 6R, 8R)‐4, 9‐Twistadien: Synthese und Bestimmung der absoluten Konfiguration

Helvetica chimica acta, 1980-07, Vol.63 (5), p.1347-1351

1980

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In vivo antitumor activity of NVP-AEW541—A novel, potent, and selective inhibitor of the IGF-IR kinase

Pharmacokinetics and Body Distribution of Liposomal Zinc Phthalocyanine in Tumor‐Bearing Mice: Influence of Aggregation State, Particle Size, and Composition

New Aza-Dipeptide Analogues as Potent and Orally Absorbed HIV-1 Protease Inhibitors: Candidates for Clinical Development

2,6,9-trisubstituted purines : Optimization towards highly potent and selective CDK1 inhibitors

Large‐Scale Production of Liposomes Containing Monomeric Zinc Phthalocyanine by Controlled Dilution of Organic Solvents

Aza-Peptide Analogs as Potent Human Immunodeficiency Virus Type-1 Protease Inhibitors with Oral Bioavailability

Structure-based design of potent CDK1 inhibitors derived from olomoucine

Synthesis of Potent and Orally Active HIV-Protease Inhibitors

Biological effects of modified colchicines. Improved preparation of 2-demethylcolchicine, 3-demethylcolchicine, and (+)-colchicine and reassignment of the position of the double bond in dehydro-7-deacetamidocolchicines

Simple Conversion of Colchicine into Demecolcine

(+)-(1S, 3S, 6S, 8S)-und (−)-(1R, 3R, 6R, 8R)-4, 9-Twistadien: Synthese und Bestimmung der absoluten Konfiguration

[2+2]-Cycloaddition von Ketenen an «Maleinisoimide» und Überführung der spiroverknüpften b̃-Laktame in Muconsäure- und Tetramsäurederivate

Cycloaddition von Chlorsulfonyliscyanat an «Maleinisoimide

Twista-4,9-diene. Preliminary communication

The Novel Adamantane Isomer 2,5-Trimethylenenorbornane (Tricycio-[5.3.0.3,9]decane, 4-Homotwistbrendane)

Synthesis of regiospecifically substituted pyrimidyl derivatives and their incorporation into penems

SYNTHESIS AND BIOLOGICAL ACTIVITY OF 2-LACTONYL PENEMS

ChemInform Abstract: 2,6,9-Trisubstituted Purines: Optimization Towards Highly Potent and Selective CDK1 Inhibitors

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 Relevant HIV Protease Inhibitors

13C- and 1H-NMR. Assignments for colchicine derivatives

S-Adenosylmethionine decarboxylase inhibitors: new aryl and heteroaryl analogs of methylglyoxal bis(guanylhydrazone)

Corrigendum to “2,6,9-trisubstituted purines: optimization towards highly potent and selective CDK1 inhibitors”

In Vitro Effect of α 1 ‐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

In Vitro Effect of α1-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

(+)‐(1S, 3S, 6S, 8S)‐und (−)‐(1R, 3R, 6R, 8R)‐4, 9‐Twistadien: Synthese und Bestimmung der absoluten Konfiguration

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