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Transglutaminase-catalyzed reaction is important for molting of Onchocerca volvulus third-stage larvae

Antimicrobial Agents and Chemotherapy, 1995-09, Vol.39 (9), p.1913-1919

1995

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Design and synthesis of SH3 domain binding ligands: Modifications of the consensus sequence XPpXP

Bioorganic & medicinal chemistry letters, 1998-11, Vol.8 (22), p.3137-3142

1998

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Matrilysin-inhibitor complexes: common themes among metalloproteases

Biochemistry (Easton), 1995-05, Vol.34 (20), p.6602-6610

1995

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Heats of formation of some simple alkyl radicals

Journal of the American Chemical Society, 1982-06, Vol.104 (13), p.3655-3659

1982

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Design and synthesis of a pyridone-based phosphotyrosine mimetic

Bioorganic & medicinal chemistry letters, 1998-10, Vol.8 (19), p.2813-2816

1998

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Heats of formation and ionization potentials of some .alpha.-aminoalkyl radicals

Journal of the American Chemical Society, 1983-07, Vol.105 (14), p.4701-4703

1983

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A new class of mechanism-based inhibitors of transglutaminase enzymes inhibits the formation of cross-linked envelopes by human malignant keratinocytes

Molecular pharmacology, 1989-05, Vol.35 (5), p.701-706

1989

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Selective A1-adenosine receptor antagonists identified using yeast Saccharomyces cerevisiae functional assays

Bioorganic & medicinal chemistry letters, 1999-08, Vol.9 (16), p.2413-2418

1999

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Structures and optical absorption spectra of some sulfuranyl radicals in solution

Journal of organic chemistry, 1985-07, Vol.50 (14), p.2516-2518

1985

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Heats of formation of tert-butyl and ethyl radicals

Journal of the American Chemical Society, 1981-07, Vol.103 (14), p.4262-4263

1981

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Study of noncovalent enzyme—inhibitor complexes and metal binding stoichiometry of matrilysin by electrospray ionization mass spectrometry

Journal of the American Society for Mass Spectrometry, 1995-11, Vol.6 (11), p.1105-1111

1995

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Allenic suicide substrates. New inhibitors of vitamin B6 linked decarboxylases

Journal of the American Chemical Society, 1984-05, Vol.106 (9), p.2734-2735

1984

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OSI-930 : A novel selective inhibitor of kit and kinase insert domain receptor tyrosine kinases with antitumor activity in mouse xenograft models

Cancer research (Chicago, Ill.), 2006-01, Vol.66 (2), p.1015-1024

2006

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Intriguing structure-activity relations underlie the potent inhibition of HIV protease by norstatine-based peptides

Journal of medicinal chemistry, 1992-04, Vol.35 (7), p.1318-1320

1992

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Do spin-adducts of 5,5-dimethylpyrroline-N-oxide dimerize?

Canadian journal of chemistry, 1982-06, Vol.60 (12), p.1501-1503

1982

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Reactions of an electrophilic glycine cation equivalent with Grignard reagents: a simple synthesis of β-γ-unsaturated amino acids

Tetrahedron letters, 1986, Vol.27 (22), p.2435-2438

1986

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A novel route to allenyl fluorides. Synthesis of 4-amino-7-fluorohepta-5,6-dienoic acid, the first fluoroallenyl amino acid

Journal of the American Chemical Society, 1987-05, Vol.109 (11), p.3491-3493

1987

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Glucokinase-activating ureas

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (5), p.1501-1504

2005

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Solid-state 13C NMR study of a transglutaminase-inhibitor adduct

Biochemistry (Easton), 1993-04, Vol.32 (15), p.3930-3934

1993

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Practical synthesis of tetrasubstituted thiophenes for use in compound libraries

Tetrahedron letters, 1999-07, Vol.40 (30), p.5471-5474

1999

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A practical solid phase synthesis of quinazoline-2,4-diones

Tetrahedron letters, 1998-10, Vol.39 (40), p.7235-7238

1998

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Leporin B: a novel hexokinase II gene inducing agent from an unidentified fungus

Bioorganic & medicinal chemistry letters, 2003-04, Vol.13 (8), p.1433-1435

2003

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Potent and selective [2-imidazol-1-yl-2-(6-alkoxy-naphthalen-2-yl)-1-methyl-ethyl]-dimethyl-amines as retinoic acid metabolic blocking agents (RAMBAs)

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (6), p.1669-1673

2005

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3-[6-(2-Dimethylamino-1-imidazol-1-yl-butyl)-naphthalen-2-yloxy]-2,2-dimethyl-propionic acid as a highly potent and selective retinoic acid metabolic blocking agent

Bioorganic & medicinal chemistry letters, 2006-05, Vol.16 (10), p.2729-2733

2006

Volltextzugriff (PDF)

Inactivation of a Cytosolic Phospholipase A2 by Thiol-Modifying Reagents: Cysteine Residues as Potential Targets of Phospholipase A2

Biochemistry (Easton), 1994-07, Vol.33 (28), p.8594-8603

1994

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Transglutaminase-catalyzed reaction is important for molting of Onchocerca volvulus third-stage larvae

Design and synthesis of SH3 domain binding ligands: Modifications of the consensus sequence XPpXP

Matrilysin-inhibitor complexes: common themes among metalloproteases

Heats of formation of some simple alkyl radicals

Design and synthesis of a pyridone-based phosphotyrosine mimetic

Heats of formation and ionization potentials of some .alpha.-aminoalkyl radicals

A new class of mechanism-based inhibitors of transglutaminase enzymes inhibits the formation of cross-linked envelopes by human malignant keratinocytes

Selective A1-adenosine receptor antagonists identified using yeast Saccharomyces cerevisiae functional assays

Structures and optical absorption spectra of some sulfuranyl radicals in solution

Heats of formation of tert-butyl and ethyl radicals

Study of noncovalent enzyme—inhibitor complexes and metal binding stoichiometry of matrilysin by electrospray ionization mass spectrometry

Allenic suicide substrates. New inhibitors of vitamin B6 linked decarboxylases

OSI-930 : A novel selective inhibitor of kit and kinase insert domain receptor tyrosine kinases with antitumor activity in mouse xenograft models

Intriguing structure-activity relations underlie the potent inhibition of HIV protease by norstatine-based peptides

Do spin-adducts of 5,5-dimethylpyrroline-N-oxide dimerize?

Reactions of an electrophilic glycine cation equivalent with Grignard reagents: a simple synthesis of β-γ-unsaturated amino acids

A novel route to allenyl fluorides. Synthesis of 4-amino-7-fluorohepta-5,6-dienoic acid, the first fluoroallenyl amino acid

Glucokinase-activating ureas

Solid-state 13C NMR study of a transglutaminase-inhibitor adduct

Practical synthesis of tetrasubstituted thiophenes for use in compound libraries

A practical solid phase synthesis of quinazoline-2,4-diones

Leporin B: a novel hexokinase II gene inducing agent from an unidentified fungus

Potent and selective [2-imidazol-1-yl-2-(6-alkoxy-naphthalen-2-yl)-1-methyl-ethyl]-dimethyl-amines as retinoic acid metabolic blocking agents (RAMBAs)

3-[6-(2-Dimethylamino-1-imidazol-1-yl-butyl)-naphthalen-2-yloxy]-2,2-dimethyl-propionic acid as a highly potent and selective retinoic acid metabolic blocking agent

Inactivation of a Cytosolic Phospholipase A2 by Thiol-Modifying Reagents: Cysteine Residues as Potential Targets of Phospholipase A2

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