UB Paderborn / Katalog / Suche / in CDI

1 – 24 von 24

Sortiert nach

The Piancatelli rearrangement: new applications for an intriguing reaction

Molecules, 2013-10, Vol.18 (10), p.12290-12312

2013

Link zum Volltext

Verfügbarkeit prüfen

A submarine journey: the pyrrole-imidazole alkaloids

Marine Drugs, 2009-11, Vol.7 (4), p.705-753

2009

Link zum Volltext

Verfügbarkeit prüfen

Total synthesis of the amaryllidaceae alkaloid (+)-plicamine using solid-supported reagents

Tetrahedron, 2002-08, Vol.58 (32), p.6285-6304

2002

Link zum Volltext

Verfügbarkeit prüfen

3-Aminopyrazole Inhibitors of CDK2/Cyclin A as Antitumor Agents. 2. Lead Optimization

Journal of medicinal chemistry, 2005-04, Vol.48 (8), p.2944-2956

2005

Link zum Volltext

Verfügbarkeit prüfen

ADME properties of CHF6366, a novel bi-functional M3 muscarinic receptor antagonist and ß2 adrenoceptor agonist (MABA) radiolabelled at both functional moieties

Xenobiotica, 2023-07, Vol.ahead-of-print (ahead-of-print), p.1-21

2023

Link zum Volltext

Verfügbarkeit prüfen

ADME properties of CHF6366, a novel bi-functional M3 muscarinic receptor antagonist and ß 2 adrenoceptor agonist (MABA) radiolabelled at both functional moieties

Xenobiotica, 2023-04, Vol.53 (4), p.288-308

2023

Link zum Volltext

Verfügbarkeit prüfen

Plasma-enhanced protein patterning in a microfluidic compartmentalized platform for multi-organs-on-chip: a liver-tumor model

Biomedical materials (Bristol), 2021-07, Vol.16 (4), p.45032

2021

Link zum Volltext

Verfügbarkeit prüfen

Stereoselective synthesis of 3,4‐dihydropyrrolo[1,2‐a]pyrazin‐1(2H)‐one derivatives as PIM kinase inhibitors inspired from marine alkaloids

Chirality (New York, N.Y.), 2022-11, Vol.34 (11), p.1437-1452

2022

Link zum Volltext

Verfügbarkeit prüfen

Identification of Shc docking site on Ret tyrosine kinase

Oncogene, 1997-02, Vol.14 (7), p.773-782

1997

Link zum Volltext

Verfügbarkeit prüfen

Stereoselective synthesis of 3,4‐dihydropyrrolopyrazin‐1(2H)‐one derivatives as PIM kinase inhibitors inspired from marine alkaloids

Chirality (New York, N.Y.), 2022-11, Vol.34 (11), p.1437-1452

2022

Link zum Volltext

Verfügbarkeit prüfen

Total Synthesis of the Amaryllidaceae Alkaloid (+)-Plicamine and Its Unnatural Enantiomer by Using Solid-Supported Reagents and Scavengers in a Multistep Sequence of Reactions We gratefully acknowledge financial support from Pfizer Central Research for a Postdoctoral Fellowship (to I.R.B.), the BP endowment and the Novartis Research Fellowship (to S.V.L.), and Pharmacia & Upjohn (to C.P.)

Angewandte Chemie International Edition, 2002-06, Vol.41 (12), p.2194

2002

Link zum Volltext

Verfügbarkeit prüfen

Total Synthesis of the Amaryllidaceae Alkaloid (+)-Plicamine and Its Unnatural Enantiomer by Using Solid-Supported Reagents and Scavengers in a Multistep Sequence of Reactions

Angewandte Chemie (International ed.), 2002-06, Vol.41 (12), p.2194-2197

2002

Link zum Volltext

Verfügbarkeit prüfen

Discovery and optimization of pyrrolo[1,2-a]pyrazinones leads to novel and selective inhibitors of PIM kinases

Bioorganic & medicinal chemistry, 2013-12, Vol.21 (23), p.7364-7380

2013

Link zum Volltext

Verfügbarkeit prüfen

3-Aminopyrazole Inhibitors of CDK2/Cyclin A as Antitumor Agents. 1. Lead Finding

Journal of medicinal chemistry, 2004-06, Vol.47 (13), p.3367-3380

2004

Link zum Volltext

Verfügbarkeit prüfen

Total Synthesis of the Amaryllidaceae Alkaloid (+)-Plicamine and Its Unnatural Enantiomer by Using Solid-Supported Reagents and Scavengers in a Multistep Sequence of Reactions We gratefully acknowledge financial support from Pfizer Central Research for a Postdoctoral Fellowship (to I.R.B.), the BP endowment and the Novartis Research Fellowship (to S.V.L.), and Pharmacia & Upjohn (to C.P.)

Angewandte Chemie, 2002-06, Vol.114 (12), p.2298

2002

Link zum Volltext

Verfügbarkeit prüfen

The Full Oncogenic Activity of Ret/ptc2 Depends on Tyrosine 539, a Docking Site for Phospholipase Cγ

Molecular and cellular biology, 1996-05, Vol.16 (5), p.2151-2163

1996

Link zum Volltext

Verfügbarkeit prüfen

ChemInform Abstract: The Piancatelli Rearrangement: New Applications for an Intriguing Reaction

ChemInform, 2014-06, Vol.45 (23), p.no-no

2014

Link zum Volltext

Verfügbarkeit prüfen

3-Aminopyrazole Inhibitors of CDK2/Cyclin A as Antitumor Agents. 2. Lead Optimization

Journal of medicinal chemistry, 2005-07, Vol.48 (15), p.5058-5058

2005

Link zum Volltext

Verfügbarkeit prüfen

3-aminopyrazole inhibitors of CDK/cyclin A as antitumor agents. 1. Lead finding

Journal of medicinal chemistry, 2004, Vol.47 (13), p.3367-3380

2004

Link zum Volltext

Verfügbarkeit prüfen

Total Synthesis of the Amaryllidaceae Alkaloid (+)-Plicamine and Its Unnatural Enantiomer by Using Solid-Supported Reagents and Scavengers in a Multistep Sequence of Reactions

Angewandte Chemie, 2002-06, Vol.114 (12), p.2298-2301

2002

Link zum Volltext

Verfügbarkeit prüfen

Phosphorylated residues as specificity determinants for an acidophilic protein tyrosine kinase: A study with src and cdc2 derived phosphopeptides

FEBS letters, 1993-09, Vol.330 (2), p.141-145

1993

Link zum Volltext

Verfügbarkeit prüfen

Phosphorylated residues as specificity determinants for an acidophilic protein tyrosine kinase

FEBS letters, 1993-09, Vol.330 (2), p.141-145

1993

Link zum Volltext

Verfügbarkeit prüfen

ChemInform Abstract: A Submarine Journey: The Pyrrole--Imidazole Alkaloids

ChemInform, 2010-05, Vol.41 (21), p.no-no

2010

Link zum Volltext

Verfügbarkeit prüfen

Total Synthesis of the Amaryllidaceae Alkaloid (+)-Plicamine Using Solid-Supported Reagents

ChemInform, 2002-12, Vol.33 (50), p.179-179

2002

Link zum Volltext

Verfügbarkeit prüfen

1 – 24 von 24

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(21)
Mit Volltextzugriff
(22)

Publikationsform

Artikel
(24)

Sprache

Englisch
(24)
Japanisch
(7)

Erscheinungsjahr

n.n

Thema

Science & Technology
(14)
Life Sciences & Biomedicine
(11)
Pharmacology & Pharmacy
(7)
Chemistry, Medicinal
(6)
Animals
(5)
Biochemistry & Molecular Biology
(5)
Chemistry
(5)
Humans
(5)
Physical Sciences
(5)
Biological And Medical Sciences
(4)
Review
(4)
Alkaloids
(3)
Cell Biology
(3)
Chemistry, Organic
(3)
Mice
(3)
Phosphorylation
(3)
Stereoisomerism
(3)
Alkylation
(2)
Antineoplastic Agents
(2)
Antineoplastic Agents - Chemical Synthesis
(2)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Journal Of Medicinal Chemistry
(4)
Angewandte Chemie
(3)
Cheminform
(3)
Angewandte Chemie International Edition
(2)
Chirality
(2)
Febs Letters
(2)
Xenobiotica
(2)
Biomedical Materials
(1)
Bioorganic & Medicinal Chemistry
(1)
Marine Drugs
(1)

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The Piancatelli rearrangement: new applications for an intriguing reaction

A submarine journey: the pyrrole-imidazole alkaloids

Total synthesis of the amaryllidaceae alkaloid (+)-plicamine using solid-supported reagents

3-Aminopyrazole Inhibitors of CDK2/Cyclin A as Antitumor Agents. 2. Lead Optimization

ADME properties of CHF6366, a novel bi-functional M3 muscarinic receptor antagonist and ß2 adrenoceptor agonist (MABA) radiolabelled at both functional moieties

ADME properties of CHF6366, a novel bi-functional M3 muscarinic receptor antagonist and ß 2 adrenoceptor agonist (MABA) radiolabelled at both functional moieties

Plasma-enhanced protein patterning in a microfluidic compartmentalized platform for multi-organs-on-chip: a liver-tumor model

Stereoselective synthesis of 3,4‐dihydropyrrolo[1,2‐a]pyrazin‐1(2H)‐one derivatives as PIM kinase inhibitors inspired from marine alkaloids

Identification of Shc docking site on Ret tyrosine kinase

Stereoselective synthesis of 3,4‐dihydropyrrolopyrazin‐1(2H)‐one derivatives as PIM kinase inhibitors inspired from marine alkaloids

Total Synthesis of the Amaryllidaceae Alkaloid (+)-Plicamine and Its Unnatural Enantiomer by Using Solid-Supported Reagents and Scavengers in a Multistep Sequence of Reactions

Discovery and optimization of pyrrolo[1,2-a]pyrazinones leads to novel and selective inhibitors of PIM kinases

3-Aminopyrazole Inhibitors of CDK2/Cyclin A as Antitumor Agents. 1. Lead Finding

The Full Oncogenic Activity of Ret/ptc2 Depends on Tyrosine 539, a Docking Site for Phospholipase Cγ

ChemInform Abstract: The Piancatelli Rearrangement: New Applications for an Intriguing Reaction

3-Aminopyrazole Inhibitors of CDK2/Cyclin A as Antitumor Agents. 2. Lead Optimization

3-aminopyrazole inhibitors of CDK/cyclin A as antitumor agents. 1. Lead finding

Total Synthesis of the Amaryllidaceae Alkaloid (+)-Plicamine and Its Unnatural Enantiomer by Using Solid-Supported Reagents and Scavengers in a Multistep Sequence of Reactions

Phosphorylated residues as specificity determinants for an acidophilic protein tyrosine kinase: A study with src and cdc2 derived phosphopeptides

Phosphorylated residues as specificity determinants for an acidophilic protein tyrosine kinase

ChemInform Abstract: A Submarine Journey: The Pyrrole--Imidazole Alkaloids

Total Synthesis of the Amaryllidaceae Alkaloid (+)-Plicamine Using Solid-Supported Reagents

Suchergebnisse filtern