UB Paderborn / Katalog / Suche / in CDI

1 – 21 von 21

Sortiert nach

In vitro pharmacological characterization of PD 166285, a new nanomolar potent and broadly active protein tyrosine kinase inhibitor

The Journal of pharmacology and experimental therapeutics, 1997-12, Vol.283 (3), p.1433

1997

Volltextzugriff (PDF)

In vitro biological characterization and antiangiogenic effects of PD 166866, a selective inhibitor of the FGF-1 receptor tyrosine kinase

The Journal of pharmacology and experimental therapeutics, 1998-07, Vol.286 (1), p.569

1998

Volltextzugriff (PDF)

Design and synthesis of potent, selective, and orally active fluorine-containing renin inhibitors

Journal of medicinal chemistry, 1992-01, Vol.35 (1), p.2-14

1992

Volltextzugriff (PDF)

INHIBITION OF FGF-1 RECEPTOR TYROSINE KINASE ACTIVITY BY PD 161570, A NEW PROTEIN-TYROSINE KINASE INHIBITOR

Life sciences (1973), 1998, Vol.62 (2), p.143-150

1998

Volltextzugriff (PDF)

Inhibition of growth factor-mediated tyrosine phosphorylation in vascular smooth muscle by PD 089828, a new synthetic protein tyrosine kinase inhibitor

The Journal of pharmacology and experimental therapeutics, 1997-06, Vol.281 (3), p.1446

1997

Volltextzugriff (PDF)

Synthesis and Structure−Activity Relationships of 7-Substituted 3-(2,6-Dichlorophenyl)-1,6-naphthyridin-2(1H)-ones as Selective Inhibitors of pp60 c -src

Journal of medicinal chemistry, 2000-08, Vol.43 (16), p.3134-3147

2000

Volltextzugriff (PDF)

Synthesis and Tyrosine Kinase Inhibitory Activity of a Series of 2-Amino-8H-pyrido[2,3-d]pyrimidines: Identification of Potent, Selective Platelet-Derived Growth Factor Receptor Tyrosine Kinase Inhibitors

Journal of medicinal chemistry, 1998-10, Vol.41 (22), p.4365-4377

1998

Volltextzugriff (PDF)

Exploring the binding preferences/specificity in the active site of human cathepsin E

Proteins, structure, function, and bioinformatics, 1995-06, Vol.22 (2), p.168-181

1995

Volltextzugriff (PDF)

Synthesis and Structure−Activity Relationships of 7-Substituted 3-(2,6-Dichlorophenyl)-1,6-naphthyridin-2(1H)-ones as Selective Inhibitors of pp60c-src

Journal of medicinal chemistry, 2000-08, Vol.43 (16), p.3134-3147

2000

Volltextzugriff (PDF)

Design and Synthesis of Renin Inhibitors: Incorporation of Transition-State Isostere Side Chains That Span from the S1 to the S3 Binding Pockets and Examination of P3-Modified Renin Inhibitors

Journal of medicinal chemistry, 1995-07, Vol.38 (15), p.2893-2905

1995

Volltextzugriff (PDF)

Synthesis and Tyrosine Kinase Inhibitory Activity of a Series of 2-Amino-8 H -pyrido[2,3- d ]pyrimidines: Identification of Potent, Selective Platelet-Derived Growth Factor Receptor Tyrosine Kinase Inhibitors

Journal of medicinal chemistry, 1998-10, Vol.41 (22), p.4365-4377

1998

Volltextzugriff (PDF)

Specificity in the binding of inhibitors to the active site of human/primate aspartic proteinases: analysis of P2-P1-P1'-P2' variation

Journal of medicinal chemistry, 1993-09, Vol.36 (18), p.2614-2620

1993

Volltextzugriff (PDF)

Renin inhibitors containing .alpha.-heteroatom amino acids as P2 residues

Journal of medicinal chemistry, 1992-03, Vol.35 (6), p.1032-1042

1992

Volltextzugriff (PDF)

Peptidomimetic inhibitors of renin incorporating topographically modified isosteres spanning the P 1(→ P 3)-P 1' sites

Bioorganic & medicinal chemistry letters, 1993-10, Vol.3 (10), p.2119-2124

1993

Volltextzugriff (PDF)

New inhibitors of human renin that contain novel replacements at the P2 site

Journal of medicinal chemistry, 1991-04, Vol.34 (4), p.1258-1271

1991

Volltextzugriff (PDF)

Disparity Between Blood Pressure and PRA Inhibition After Administration of a Renin Inhibitor to Anesthetized Dogs: Methodological Considerations

Clinical and experimental hypertension (1993), 1993-01, Vol.15 (4), p.663-681

1993

Volltextzugriff (PDF)

Ethnic cultural value typologies and mental health parameters among Indians

International journal of intercultural relations, 2022-01, Vol.86, p.95-108

2022

Volltextzugriff (PDF)

In vitro reactivity of penicilloyl and penicillanyl albumin and polylysine conjugates with IgE-antibody

Journal of immunological methods, 2000-08, Vol.242 (1), p.43-51

2000

Volltextzugriff (PDF)

Video Pasaporte Español

The Modern Language Journal, 1990, Vol.74 (1), p.127-128

McAlpine, Dave

1990

Volltextzugriff (PDF)

Book reviews

Local Government Studies, 1994, Vol.20 (2), p.318-333

1994

Volltextzugriff (PDF)

Book reviews

Local Government Studies, 1994, Vol.20 (2), p.318-333

1994

Volltextzugriff (PDF)

1 – 21 von 21

Suche als RSS-Feed

Aktive Filter

SpracheJapanisch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(21)
Mit Volltextzugriff
(18)

Publikationsform

Artikel
(18)
Reviews
(3)

Sprache

Englisch
(21)

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

In vitro pharmacological characterization of PD 166285, a new nanomolar potent and broadly active protein tyrosine kinase inhibitor

In vitro biological characterization and antiangiogenic effects of PD 166866, a selective inhibitor of the FGF-1 receptor tyrosine kinase

Design and synthesis of potent, selective, and orally active fluorine-containing renin inhibitors

INHIBITION OF FGF-1 RECEPTOR TYROSINE KINASE ACTIVITY BY PD 161570, A NEW PROTEIN-TYROSINE KINASE INHIBITOR

Inhibition of growth factor-mediated tyrosine phosphorylation in vascular smooth muscle by PD 089828, a new synthetic protein tyrosine kinase inhibitor

Synthesis and Structure−Activity Relationships of 7-Substituted 3-(2,6-Dichlorophenyl)-1,6-naphthyridin-2(1H)-ones as Selective Inhibitors of pp60 c -src

Synthesis and Tyrosine Kinase Inhibitory Activity of a Series of 2-Amino-8H-pyrido[2,3-d]pyrimidines: Identification of Potent, Selective Platelet-Derived Growth Factor Receptor Tyrosine Kinase Inhibitors

Exploring the binding preferences/specificity in the active site of human cathepsin E

Synthesis and Structure−Activity Relationships of 7-Substituted 3-(2,6-Dichlorophenyl)-1,6-naphthyridin-2(1H)-ones as Selective Inhibitors of pp60c-src

Design and Synthesis of Renin Inhibitors: Incorporation of Transition-State Isostere Side Chains That Span from the S1 to the S3 Binding Pockets and Examination of P3-Modified Renin Inhibitors

Synthesis and Tyrosine Kinase Inhibitory Activity of a Series of 2-Amino-8 H -pyrido[2,3- d ]pyrimidines: Identification of Potent, Selective Platelet-Derived Growth Factor Receptor Tyrosine Kinase Inhibitors

Specificity in the binding of inhibitors to the active site of human/primate aspartic proteinases: analysis of P2-P1-P1'-P2' variation

Renin inhibitors containing .alpha.-heteroatom amino acids as P2 residues

Peptidomimetic inhibitors of renin incorporating topographically modified isosteres spanning the P 1(→ P 3)-P 1' sites

New inhibitors of human renin that contain novel replacements at the P2 site

Disparity Between Blood Pressure and PRA Inhibition After Administration of a Renin Inhibitor to Anesthetized Dogs: Methodological Considerations

Ethnic cultural value typologies and mental health parameters among Indians

In vitro reactivity of penicilloyl and penicillanyl albumin and polylysine conjugates with IgE-antibody

Video Pasaporte Español

Book reviews

Book reviews

Aktive Filter

Suchergebnisse filtern