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Binding Mode of the 4-Anilinoquinazoline Class of Protein Kinase Inhibitor: X-ray Crystallographic Studies of 4-Anilinoquinazolines Bound to Cyclin-Dependent Kinase 2 and p38 Kinase

Journal of medicinal chemistry, 2000-01, Vol.43 (1), p.133-138

2000

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Oxindole-Based Inhibitors of Cyclin-Dependent Kinase 2 (CDK2): Design, Synthesis, Enzymatic Activities, and X-ray Crystallographic Analysis

Journal of medicinal chemistry, 2001-12, Vol.44 (25), p.4339-4358

2001

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X-ray Crystal Structures of Candida albicans Dihydrofolate Reductase: High Resolution Ternary Complexes in Which the Dihydronicotinamide Moiety of NADPH Is Displaced by an Inhibitor

Journal of medicinal chemistry, 2001-08, Vol.44 (18), p.2928-2932

2001

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Recent applications of protein crystallography and structure-guided drug design

Current opinion in chemical biology, 2005-08, Vol.9 (4), p.371-380

2005

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Basis of Selectivity of Antibacterial Diaminopyrimidines

Journal of chemotherapy, 1993-12, Vol.5 (6), p.393-399

1993

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High-Affinity Inhibitors of Dihydrofolate Reductase: Antimicrobial and Anticancer Activities of 7,8-Dialkyl-1,3-diaminopyrrolo[3,2-f]quinazolines with Small Molecular Size

Journal of medicinal chemistry, 1996-02, Vol.39 (4), p.892-903

1996

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Selective Inhibitors of Candida albicans Dihydrofolate Reductase: Activity and Selectivity of 5-(Arylthio)-2,4-diaminoquinazolines

Journal of medicinal chemistry, 1995-09, Vol.38 (18), p.3608-3616

1995

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X-ray crystallographic studies of Candida albicans dihydrofolate reductase. High resolution structures of the holoenzyme and an inhibited ternary complex

The Journal of biological chemistry, 1997-11, Vol.272 (48), p.30289-30298

1997

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Prevention of Chemotherapy-Induced Alopecia in Rats by CDK Inhibitors

Science (American Association for the Advancement of Science), 2001-01, Vol.291 (5501), p.134-137

2001

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Pyrrolo[2,3- d]pyrimidines and pyrido[2,3- d]pyrimidines as conformationally restricted analogues of the antibacterial agent trimethoprim

Bioorganic & medicinal chemistry, 1996-04, Vol.4 (4), p.593-602

1996

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Receptor-based design of dihydrofolate reductase inhibitors: comparison of crystallographically determined enzyme binding with enzyme affinity in a series of carboxy-substituted trimethoprim analogs

Journal of medicinal chemistry, 1985-03, Vol.28 (3), p.303-311

1985

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Synthesis of 1,3-diamino-7,8,9,10-tetrahydropyrido[3,2-f]-quinazolines. Inhibitors of Candida albicans dihydrofolate reductase as potential antifungal agents

Journal of heterocyclic chemistry, 1997-01, Vol.34 (1), p.145-151

1997

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Resolving crystal polymorphisms by finding “stationary points” from quantitative analysis of crystal growth response surfaces

Journal of crystal growth, 1996, Vol.168 (1), p.155-169

1996

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The amino acid sequence and configuration of tentoxin

Biochemical and biophysical research communications, 1974-01, Vol.56 (1), p.234-240

1974

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Site-specific Conjugation on Serine → Cysteine Variant Monoclonal Antibodies

The Journal of biological chemistry, 2000-09, Vol.275 (39), p.30445-30450

2000

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Free energy calculations on calcium and magnesium complexes: Protein and phospholipid model systems

Journal of computational chemistry, 1991-09, Vol.12 (7), p.899-908

1991

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Free energy calculations on the relative solvation free energies of benzene, anisole, and 1,2,3-trimethoxybenzene: theoretical and experimental analysis of aromatic methoxy solvation

Journal of physical chemistry (1952), 1991-08, Vol.95 (17), p.6661-6666

1991

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Receptor-based design of dihydrofolate reductase inhibitors: comparison of crystallographically determined enzyme binding with enzyme affinity in a series of carboxy-substituted trimethoprim analogs

Journal of medicinal chemistry, 1982-10, Vol.25 (10), p.1120-1122

1982

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Site-specific conjugation on serine right-arrow cysteine variant monoclonal antibodies

The Journal of biological chemistry, 2000-09, Vol.275 (39), p.30445

2000

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Site-specific Conjugation on Serine arrow right Cysteine Variant Monoclonal Antibodies

The Journal of biological chemistry, 2000-09, Vol.275 (39), p.30445-30450

2000

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Dihydrotentoxin: a cyclic tetrapeptide

Acta Crystallographica Section B, 1981-05, Vol.37 (5), p.1139-1141

1981

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Use of 1-H nuclear magnetic resonance spectroscopy for sequence and configuration analysis of cyclic tetrapeptides. The structure of Tentoxin-1,2a--d

Journal of the American Chemical Society, 1975-06, Vol.97 (13), p.3202

1975

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Theoretical investigations of the rotational barrier in anisole: an ab initio and molecular dynamics study

Journal of physical chemistry (1952), 1990-05, Vol.94 (11), p.4483-4491

1990

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The conformations of trimethoprim/E. coli dihydrofolate reductase complexes: A super(15)N and super(31)P NMR study

FEBS letters, 1991-01, Vol.283 (1), p.44-46

1991

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High-affinity inhibitors of dihydrofolate reductase : antimicrobial and anticancer activities of 7,8-dialkyl-1,3-diaminopyrrolo[3,2-f]quinazolines with small molecular size

Journal of medicinal chemistry, 1995, Vol.39 (4), p.892-903

1995

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Binding Mode of the 4-Anilinoquinazoline Class of Protein Kinase Inhibitor: X-ray Crystallographic Studies of 4-Anilinoquinazolines Bound to Cyclin-Dependent Kinase 2 and p38 Kinase

Oxindole-Based Inhibitors of Cyclin-Dependent Kinase 2 (CDK2): Design, Synthesis, Enzymatic Activities, and X-ray Crystallographic Analysis

X-ray Crystal Structures of Candida albicans Dihydrofolate Reductase: High Resolution Ternary Complexes in Which the Dihydronicotinamide Moiety of NADPH Is Displaced by an Inhibitor

Recent applications of protein crystallography and structure-guided drug design

Basis of Selectivity of Antibacterial Diaminopyrimidines

High-Affinity Inhibitors of Dihydrofolate Reductase: Antimicrobial and Anticancer Activities of 7,8-Dialkyl-1,3-diaminopyrrolo[3,2-f]quinazolines with Small Molecular Size

Selective Inhibitors of Candida albicans Dihydrofolate Reductase: Activity and Selectivity of 5-(Arylthio)-2,4-diaminoquinazolines

X-ray crystallographic studies of Candida albicans dihydrofolate reductase. High resolution structures of the holoenzyme and an inhibited ternary complex

Prevention of Chemotherapy-Induced Alopecia in Rats by CDK Inhibitors

Pyrrolo[2,3- d]pyrimidines and pyrido[2,3- d]pyrimidines as conformationally restricted analogues of the antibacterial agent trimethoprim

Receptor-based design of dihydrofolate reductase inhibitors: comparison of crystallographically determined enzyme binding with enzyme affinity in a series of carboxy-substituted trimethoprim analogs

Synthesis of 1,3-diamino-7,8,9,10-tetrahydropyrido[3,2-f]-quinazolines. Inhibitors of Candida albicans dihydrofolate reductase as potential antifungal agents

Resolving crystal polymorphisms by finding “stationary points” from quantitative analysis of crystal growth response surfaces

The amino acid sequence and configuration of tentoxin

Site-specific Conjugation on Serine → Cysteine Variant Monoclonal Antibodies

Free energy calculations on calcium and magnesium complexes: Protein and phospholipid model systems

Free energy calculations on the relative solvation free energies of benzene, anisole, and 1,2,3-trimethoxybenzene: theoretical and experimental analysis of aromatic methoxy solvation

Receptor-based design of dihydrofolate reductase inhibitors: comparison of crystallographically determined enzyme binding with enzyme affinity in a series of carboxy-substituted trimethoprim analogs

Site-specific conjugation on serine right-arrow cysteine variant monoclonal antibodies

Site-specific Conjugation on Serine arrow right Cysteine Variant Monoclonal Antibodies

Dihydrotentoxin: a cyclic tetrapeptide

Use of 1-H nuclear magnetic resonance spectroscopy for sequence and configuration analysis of cyclic tetrapeptides. The structure of Tentoxin-1,2a--d

Theoretical investigations of the rotational barrier in anisole: an ab initio and molecular dynamics study

The conformations of trimethoprim/E. coli dihydrofolate reductase complexes: A super(15)N and super(31)P NMR study

High-affinity inhibitors of dihydrofolate reductase : antimicrobial and anticancer activities of 7,8-dialkyl-1,3-diaminopyrrolo[3,2-f]quinazolines with small molecular size

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