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Selective FLT3 inhibition of FLT3-ITD+ acute myeloid leukaemia resulting in secondary D835Y mutation: a model for emerging clinical resistance patterns

Leukemia, 2012-07, Vol.26 (7), p.1462-1470

2012

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Crystal structure of an Aurora-A mutant that mimics Aurora-B bound to MLN8054: insights into selectivity and drug design

Biochemical journal, 2010-05, Vol.427 (3), p.551-551

2010

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Selective FLT3 inhibition of [FLT3-ITD.sup.+] acute myeloid leukaemia resulting in secondary D835Y mutation: a model for emerging clinical resistance patterns

Leukemia, 2012-07, Vol.26 (7), p.1462

2012

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Synthesis of resorcinylic macrocycles related to radicicol via ring-closing metathesis

Tetrahedron letters, 2006-03, Vol.47 (13), p.2241-2243

2006

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Reusable resin plug-bound palladium catalysts for organic synthesis

Tetrahedron letters, 2003-06, Vol.44 (25), p.4779-4782

2003

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On the rational design of renin inhibitors: x-ray studies of aspartic proteinases complexed with transition-state analogs

Biochemistry (Easton), 1987-09, Vol.26 (18), p.5585-5590

1987

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Selective FLT3 inhibition of FLT3-ITD super(+) acute myeloid leukaemia resulting in secondary D835Y mutation: a model for emerging clinical resistance patterns

Leukemia, 2012-07, Vol.26 (7), p.1462-1470

2012

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Revolutionizing Resin Handling for Combinatorial Synthesis

Angewandte Chemie (International ed.), 2001-03, Vol.40 (5), p.938-941

2001

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X-ray-crystallographic studies of complexes of pepstatin A and a statine-containing human renin inhibitor with endothiapepsin

Biochemical journal, 1993-01, Vol.289 (2), p.363-371

1993

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Development of synthetic routes to macrocyclic compounds based on the HSP90 inhibitor radicicol

Tetrahedron letters, 2006-03, Vol.47 (13), p.2237-2240

2006

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Potent new inhibitors of human renin

Nature (London), 1982-10, Vol.299 (5883), p.555-557

1982

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High resolution X-ray analyses of renin inhibitor-aspartic proteinase complexes

Nature (London), 1987-05, Vol.327 (6120), p.349-352

1987

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Nail biting in rheumatic diseases

Clinical rheumatology, 1995-01, Vol.14 (1), p.93-94

1995

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A new bio-compatible pH cleavable linker for solid-phase synthesis of a squalamine analogue

Tetrahedron letters, 2001-08, Vol.42 (35), p.6211-6214

2001

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A pH cleavable linker for zone diffusion assays and single bead solution screens in combinatorial chemistry

Chemical communications (Cambridge, England), 1997 (15), p.1397-1398

1997

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Specific Inhibitors of Renin

Prague, Czechoslovakia, August 29–September 3, 1982, 2019, Vol.17., p.635-638

2019

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2-cyanopyrrolidides as potent, stable inhibitors of dipeptidyl peptidase IV

Bioorganic & medicinal chemistry letters, 1996-05, Vol.6 (10), p.1163-1166

1996

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Application of Phosphinic Acids to Peptide Synthesis

Prague, Czechoslovakia, August 29–September 3, 1982, 2019, Vol.17., p.157-162

2019

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Human renin inhibitors

Biochemical Society transactions, 1985-12, Vol.13 (6), p.1029-1032

1985

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4-cyanothiazolidides as very potent, stable inhibitors of dipeptidyl peptidase IV

Bioorganic & medicinal chemistry letters, 1996-11, Vol.6 (22), p.2745-2748

1996

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Inhibitors of aspartic proteinases and their relevance to the design of antihypertensive agents

Biochemical Society transactions, 1987-08, Vol.15 (4), p.751-754

1987

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Crystallographic Studies of Reduced Bond Inhibitors Complexed with an Aspartic Proteinase

Journal of cardiovascular pharmacology, 1987, Vol.10 Suppl 7, p.59-68

1987

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Renin Inhibitors: Their Use in Understanding the Role of Angiotensin II as a Pressor Hormone

Journal of cardiovascular pharmacology, 1985, Vol.7 Suppl 4, p.S49-S52

1985

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Thrombin Inhibitors Based on Ketone Derivatives of Arginine and Lysine

Journal of enzyme inhibition, 1995, Vol.9 (1), p.43-60

1995

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A Study of Organophosphorus Reagents in Peptide Synthesis

Atrash, B

1981

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Selective FLT3 inhibition of FLT3-ITD+ acute myeloid leukaemia resulting in secondary D835Y mutation: a model for emerging clinical resistance patterns

Crystal structure of an Aurora-A mutant that mimics Aurora-B bound to MLN8054: insights into selectivity and drug design

Selective FLT3 inhibition of [FLT3-ITD.sup.+] acute myeloid leukaemia resulting in secondary D835Y mutation: a model for emerging clinical resistance patterns

Synthesis of resorcinylic macrocycles related to radicicol via ring-closing metathesis

Reusable resin plug-bound palladium catalysts for organic synthesis

On the rational design of renin inhibitors: x-ray studies of aspartic proteinases complexed with transition-state analogs

Selective FLT3 inhibition of FLT3-ITD super(+) acute myeloid leukaemia resulting in secondary D835Y mutation: a model for emerging clinical resistance patterns

Revolutionizing Resin Handling for Combinatorial Synthesis

X-ray-crystallographic studies of complexes of pepstatin A and a statine-containing human renin inhibitor with endothiapepsin

Development of synthetic routes to macrocyclic compounds based on the HSP90 inhibitor radicicol

Potent new inhibitors of human renin

High resolution X-ray analyses of renin inhibitor-aspartic proteinase complexes

Nail biting in rheumatic diseases

A new bio-compatible pH cleavable linker for solid-phase synthesis of a squalamine analogue

A pH cleavable linker for zone diffusion assays and single bead solution screens in combinatorial chemistry

Specific Inhibitors of Renin

2-cyanopyrrolidides as potent, stable inhibitors of dipeptidyl peptidase IV

Application of Phosphinic Acids to Peptide Synthesis

Human renin inhibitors

4-cyanothiazolidides as very potent, stable inhibitors of dipeptidyl peptidase IV

Inhibitors of aspartic proteinases and their relevance to the design of antihypertensive agents

Crystallographic Studies of Reduced Bond Inhibitors Complexed with an Aspartic Proteinase

Renin Inhibitors: Their Use in Understanding the Role of Angiotensin II as a Pressor Hormone

Thrombin Inhibitors Based on Ketone Derivatives of Arginine and Lysine

A Study of Organophosphorus Reagents in Peptide Synthesis

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