UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 130

Sortiert nach

G-protein coupled receptors bivalent ligands and drug design

Expert opinion on therapeutic patents, 1999-04, Vol.9 (4), p.431-446

Halazy, Serge

1999

Volltextzugriff (PDF)

9-(Difluorophosphonoalkyl)guanines as a new class of multisubstrate analog inhibitors of purine nucleoside phosphorylase

Journal of the American Chemical Society, 1991-01, Vol.113 (1), p.315-317

1991

Volltextzugriff (PDF)

Design and Synthesis of the First Generation of Novel Potent, Selective, and in Vivo Active (Benzothiazol-2-yl)acetonitrile Inhibitors of the c-Jun N-Terminal Kinase

Journal of medicinal chemistry, 2005-07, Vol.48 (14), p.4596-4607

2005

Volltextzugriff (PDF)

3,6-Dibromocarbazole Piperazine Derivatives of 2-Propanol as First Inhibitors of Cytochrome c Release via Bax Channel Modulation

Journal of medicinal chemistry, 2003-10, Vol.46 (21), p.4365-4368

2003

Volltextzugriff (PDF)

Chemical genetics: toward the next generation of molecular medicines

Pharmacogenomics, 2004-10, Vol.5 (7), p.757-761

Halazy, Serge

2004

Volltextzugriff (PDF)

Sulfonamide derivatives of benzylamine block cholesterol biosynthesis in HepG2 cells : A new type of potent squalene epoxidase inhibitors

Bioorganic & medicinal chemistry letters, 1998-06, Vol.8 (11), p.1337-1342

1998

Volltextzugriff (PDF)

Design and synthesis of new hypocholesterolemic organosilanes with antioxidant properties

Bioorganic & medicinal chemistry letters, 1996-03, Vol.6 (5), p.533-538

1996

Volltextzugriff (PDF)

Signal Transduction: An Exciting Field of Investigation for Small Molecule Drug Discovery

Molecules (Basel, Switzerland), 2003-04, Vol.8 (4), p.349-358

Halazy, Serge

2003

Volltextzugriff (PDF)

Design, Synthesis, and Biological Activity of Novel, Potent, and Selective (Benzoylaminomethyl)thiophene Sulfonamide Inhibitors of c-Jun-N-Terminal Kinase

Journal of medicinal chemistry, 2004-12, Vol.47 (27), p.6921-6934

2004

Volltextzugriff (PDF)

Design and synthesis of new potential photoaffinity labels for mammalian squalene epoxidase

Bioorganic & medicinal chemistry letters, 1997-05, Vol.7 (9), p.1153-1156

1997

Volltextzugriff (PDF)

1,1-Difluoroalkyl glucosides: a new class of enzyme-activated irreversible inhibitors of .alpha.-glucosidases

Journal of the American Chemical Society, 1989-04, Vol.111 (9), p.3484-3485

1989

Volltextzugriff (PDF)

Ortho- and para-(difluoromethyl)aryl-β- d-glucosides: A new class of enzyme-activated irreversible inhibitors of β-glucosidases

Bioorganic chemistry, 1990, Vol.18 (3), p.330-344

1990

Volltextzugriff (PDF)

Arylpiperazide derivatives of phenylpiperazines as a new class of potent and selective 5-HT1B receptor antagonists

Bioorganic & medicinal chemistry letters, 1997-12, Vol.7 (24), p.3183-3188

1997

Volltextzugriff (PDF)

Inhibition of farnesyl protein transferase by new farnesyl phosphonate derivatives of phenylalanine

Bioorganic & medicinal chemistry letters, 1996-06, Vol.6 (12), p.1291-1296

1996

Volltextzugriff (PDF)

Synthesis of new carbocyclic phosphonate analogs of dideoxypurine nucleotides

Tetrahedron letters, 1991-10, Vol.32 (44), p.6341-6344

1991

Volltextzugriff (PDF)

Discovery and Development of a New Class of Potent, Selective, Orally Active Oxytocin Receptor Antagonists

Journal of medicinal chemistry, 2005-12, Vol.48 (24), p.7882-7905

2005

Volltextzugriff (PDF)

Dimers of 5HT1 ligands preferentially bind to 5HT1B/1D receptor subtypes

Bioorganic & medicinal chemistry letters, 1998-06, Vol.8 (11), p.1407-1412

1998

Volltextzugriff (PDF)

Synthesis and Antiviral Properties of New Cycloalkanol Derivatives of Guanine

Nucleosides & nucleotides, 1992-11, Vol.11 (9), p.1595-1606

1992

Volltextzugriff (PDF)

A Simple One-Pot Preparation of N,N’-Unsymmetrical Ureas from N-Boc Protected Primary Anilines and Amines

Synlett, 1996-06, Vol.1996 (6), p.507-508

1996

Volltextzugriff (PDF)

α-Selenocyclobutyllithium as a 2-lithio-1,3-diene equivalent. regioselective (100%) synthesis of ipsenol

Tetrahedron letters, 1980, Vol.21 (20), p.1997-2000

1980

Volltextzugriff (PDF)

Synthetic routes to cyclopropylidenecarbinols and to cyclopropylidienes

Tetrahedron letters, 1981, Vol.22 (22), p.2135-2138

1981

Volltextzugriff (PDF)

New rearrangement of the adducts formed from allenes and benzeneselenenyl halides

Tetrahedron letters, 1983, Vol.24 (26), p.2689-2692

1983

Volltextzugriff (PDF)

A new general route to olefins from selenides

Tetrahedron letters, 1979, Vol.20 (43), p.4233-4236

1979

Volltextzugriff (PDF)

Regio and stereoselective synthesis of 1-methylseleno-1-vinyl and 1-phenylseleno-1-vinyl cyclopropanes

Tetrahedron letters, 1981, Vol.22 (19), p.1833-1836

1981

Volltextzugriff (PDF)

Serotonin dimers: application of the bivalent ligand approach to the design of new potent and selective 5-HT(1B/1D) agonists

Journal of medicinal chemistry, 1996-12, Vol.39 (25), p.4920-4927

1996

Volltextzugriff (PDF)

1 – 25 von 130

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(96)
Mit Volltextzugriff
(110)

Publikationsform

Artikel
(130)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(59)
Chemistry
(37)
Life Sciences & Biomedicine
(35)
Physical Sciences
(34)
Chemistry, Organic
(28)
Pharmacology & Pharmacy
(27)
Chemistry, Medicinal
(21)
Animals
(20)
Biological And Medical Sciences
(20)
Medical Sciences
(19)
Pharmacology. Drug Treatments
(19)
Humans
(16)
Organic Chemistry
(14)
Exact Sciences And Technology
(13)
Medicinal Chemistry
(13)
Pharmacology
(13)
Pharmacology, Medicinal Chemistry, Vaccines, Serums
(13)
Serums
(13)
Vaccines
(13)
Neuropharmacology
(10)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

G-protein coupled receptors bivalent ligands and drug design

9-(Difluorophosphonoalkyl)guanines as a new class of multisubstrate analog inhibitors of purine nucleoside phosphorylase

Design and Synthesis of the First Generation of Novel Potent, Selective, and in Vivo Active (Benzothiazol-2-yl)acetonitrile Inhibitors of the c-Jun N-Terminal Kinase

3,6-Dibromocarbazole Piperazine Derivatives of 2-Propanol as First Inhibitors of Cytochrome c Release via Bax Channel Modulation

Chemical genetics: toward the next generation of molecular medicines

Sulfonamide derivatives of benzylamine block cholesterol biosynthesis in HepG2 cells : A new type of potent squalene epoxidase inhibitors

Design and synthesis of new hypocholesterolemic organosilanes with antioxidant properties

Signal Transduction: An Exciting Field of Investigation for Small Molecule Drug Discovery

Design, Synthesis, and Biological Activity of Novel, Potent, and Selective (Benzoylaminomethyl)thiophene Sulfonamide Inhibitors of c-Jun-N-Terminal Kinase

Design and synthesis of new potential photoaffinity labels for mammalian squalene epoxidase

1,1-Difluoroalkyl glucosides: a new class of enzyme-activated irreversible inhibitors of .alpha.-glucosidases

Ortho- and para-(difluoromethyl)aryl-β- d-glucosides: A new class of enzyme-activated irreversible inhibitors of β-glucosidases

Arylpiperazide derivatives of phenylpiperazines as a new class of potent and selective 5-HT1B receptor antagonists

Inhibition of farnesyl protein transferase by new farnesyl phosphonate derivatives of phenylalanine

Synthesis of new carbocyclic phosphonate analogs of dideoxypurine nucleotides

Discovery and Development of a New Class of Potent, Selective, Orally Active Oxytocin Receptor Antagonists

Dimers of 5HT1 ligands preferentially bind to 5HT1B/1D receptor subtypes

Synthesis and Antiviral Properties of New Cycloalkanol Derivatives of Guanine

A Simple One-Pot Preparation of N,N’-Unsymmetrical Ureas from N-Boc Protected Primary Anilines and Amines

α-Selenocyclobutyllithium as a 2-lithio-1,3-diene equivalent. regioselective (100%) synthesis of ipsenol

Synthetic routes to cyclopropylidenecarbinols and to cyclopropylidienes

New rearrangement of the adducts formed from allenes and benzeneselenenyl halides

A new general route to olefins from selenides

Regio and stereoselective synthesis of 1-methylseleno-1-vinyl and 1-phenylseleno-1-vinyl cyclopropanes

Serotonin dimers: application of the bivalent ligand approach to the design of new potent and selective 5-HT(1B/1D) agonists

Suchergebnisse filtern