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The development of new isoxazolone based inhibitors of tumor necrosis factor-alpha (TNF-α) production

Bioorganic & medicinal chemistry letters, 2005-05, Vol.15 (9), p.2399-2403

2005

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Development of New Carboxylic Acid-Based MMP Inhibitors Derived from Functionalized Propargylglycines

Journal of medicinal chemistry, 2001-03, Vol.44 (7), p.1060-1071

2001

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Synthesis, Aggregation, and Chiroptical Properties of Chiral, Amphiphilic Dendrimers

Journal of organic chemistry, 2001-09, Vol.66 (19), p.6440-6452

2001

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Development of Orally Bioavailable Bicyclic Pyrazolones as Inhibitors of Tumor Necrosis Factor-α Production

Journal of medicinal chemistry, 2004-05, Vol.47 (11), p.2724-2727

2004

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The development of 2-benzimidazole substituted pyrimidine based inhibitors of lymphocyte specific kinase (Lck)

Bioorganic & medicinal chemistry letters, 2006-12, Vol.16 (23), p.5973-5977

2006

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Development of new pyrrolopyrimidine-based inhibitors of Janus kinase 3 (JAK3)

Bioorganic & medicinal chemistry letters, 2007-03, Vol.17 (5), p.1250-1253

2007

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The development of new carboxylic acid-based MMP inhibitors derived from a cyclohexylglycine scaffold

Bioorganic & medicinal chemistry letters, 2001-08, Vol.11 (15), p.1975-1979

2001

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The development of novel 1,2-dihydro-pyrimido[4,5- c]pyridazine based inhibitors of lymphocyte specific kinase (Lck)

Bioorganic & medicinal chemistry letters, 2006-08, Vol.16 (16), p.4257-4261

2006

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Development of N-4,6-pyrimidine- N-alkyl- N′-phenyl ureas as orally active inhibitors of lymphocyte specific tyrosine kinase

Bioorganic & medicinal chemistry letters, 2006-07, Vol.16 (14), p.3646-3650

2006

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The development of monocyclic pyrazolone based cytokine synthesis inhibitors

Bioorganic & medicinal chemistry letters, 2005-05, Vol.15 (9), p.2285-2289

2005

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Development of N-2,4-pyrimidine-N-phenyl-N′-phenyl ureas as inhibitors of tumor necrosis factor alpha (TNF-α) synthesis. Part 1

Bioorganic & medicinal chemistry letters, 2006-07, Vol.16 (13), p.3510-3513

2006

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The development of novel C-2, C-8, and N-9 trisubstituted purines as inhibitors of TNF-α production

Bioorganic & medicinal chemistry letters, 2006-08, Vol.16 (16), p.4360-4365

2006

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The development of novel inhibitors of tumor necrosis factor-α (TNF-α) production based on substituted [5,5]-bicyclic pyrazolones

Bioorganic & medicinal chemistry letters, 2004-08, Vol.14 (16), p.4267-4272

2004

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Development of N-2,4-pyrimidine-N-phenyl-N′-alkyl ureas as orally active inhibitors of tumor necrosis factor alpha (TNF-α) synthesis. Part 2

Bioorganic & medicinal chemistry letters, 2006-07, Vol.16 (13), p.3514-3518

2006

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The development of new bicyclic pyrazole-based cytokine synthesis inhibitors

Bioorganic & medicinal chemistry letters, 2004-10, Vol.14 (19), p.4945-4948

2004

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Synthesis and Chiroptical Properties of Dendrimers Elaborated from a Chiral, Nonracemic Central Core

Journal of organic chemistry, 1998-12, Vol.63 (25), p.9399-9405

1998

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Synthesis of Novel Pyrimido[4,5-c]pyridazines and 1,2-Dihydro-3a,7,9,9b-Tetraaza-cyclopenta[a]naphthalen-3-ones as Potent Inhibitors of Lymphocyte Specific Kinase (LCK)

Heterocycles, 2006-10, Vol.68 (10), p.2037

2006

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Chemoenzymatic synthesis of functionalized cyclohexylglycines and α-methylcyclohexylglycines via Kazmaier–Claisen rearrangement

Bioorganic & medicinal chemistry letters, 2001-03, Vol.11 (5), p.627-629

2001

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Convergent synthesis of 2,3-bisarylpyrazolones through cyclization of bisacylated pyrazolidines and hydrazines

Tetrahedron letters, 2006-05, Vol.47 (19), p.3195-3198

2006

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Corrigendum to “Development of N-2,4-pyrimidine- N-phenyl- N′-phenyl ureas as inhibitors of tumor necrosis factor alpha (TNF-α) synthesis. Part 1” [Bioorg. Med. Chem. Lett. 16 (2006) 3510–3513]

Bioorganic & medicinal chemistry letters, 2006-09, Vol.16 (17), p.4700-4700

2006

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The Development of Novel Inhibitors of Tumor Necrosis Factor-α (TNF-α) Production Based on Substituted [5,5]-Bicyclic Pyrazolones

ChemInform, 2004-12, Vol.35 (49), p.no-no

2004

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Synthesis of Novel Pyrimido[4,5-c]pyridazines and 1,2-Dihydro-3a,7,9,9b-tetraaza-cyclopenta[a]naphthalen-3-ones as Potent Inhibitors of Lymphocyte Specific Kinase (LCK)

ChemInform, 2007-02, Vol.38 (6), p.no-no

2007

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ChemInform Abstract: Chemoenzymatic Synthesis of Functionalized Cyclohexylglycines and α-Methylcyclohexylglycines via Kazmaier-Claisen Rearrangement

ChemInform, 2001-06, Vol.32 (24), p.no-no

2001

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The development of new isoxazolone based inhibitors of tumor necrosis factor-alpha (TNF-α) production

Development of New Carboxylic Acid-Based MMP Inhibitors Derived from Functionalized Propargylglycines

Synthesis, Aggregation, and Chiroptical Properties of Chiral, Amphiphilic Dendrimers

Development of Orally Bioavailable Bicyclic Pyrazolones as Inhibitors of Tumor Necrosis Factor-α Production

The development of 2-benzimidazole substituted pyrimidine based inhibitors of lymphocyte specific kinase (Lck)

Development of new pyrrolopyrimidine-based inhibitors of Janus kinase 3 (JAK3)

The development of new carboxylic acid-based MMP inhibitors derived from a cyclohexylglycine scaffold

The development of novel 1,2-dihydro-pyrimido[4,5- c]pyridazine based inhibitors of lymphocyte specific kinase (Lck)

Development of N-4,6-pyrimidine- N-alkyl- N′-phenyl ureas as orally active inhibitors of lymphocyte specific tyrosine kinase

The development of monocyclic pyrazolone based cytokine synthesis inhibitors

Development of N-2,4-pyrimidine-N-phenyl-N′-phenyl ureas as inhibitors of tumor necrosis factor alpha (TNF-α) synthesis. Part 1

The development of novel C-2, C-8, and N-9 trisubstituted purines as inhibitors of TNF-α production

The development of novel inhibitors of tumor necrosis factor-α (TNF-α) production based on substituted [5,5]-bicyclic pyrazolones

Development of N-2,4-pyrimidine-N-phenyl-N′-alkyl ureas as orally active inhibitors of tumor necrosis factor alpha (TNF-α) synthesis. Part 2

The development of new bicyclic pyrazole-based cytokine synthesis inhibitors

Synthesis and Chiroptical Properties of Dendrimers Elaborated from a Chiral, Nonracemic Central Core

Synthesis of Novel Pyrimido[4,5-c]pyridazines and 1,2-Dihydro-3a,7,9,9b-Tetraaza-cyclopenta[a]naphthalen-3-ones as Potent Inhibitors of Lymphocyte Specific Kinase (LCK)

Chemoenzymatic synthesis of functionalized cyclohexylglycines and α-methylcyclohexylglycines via Kazmaier–Claisen rearrangement

Convergent synthesis of 2,3-bisarylpyrazolones through cyclization of bisacylated pyrazolidines and hydrazines

Corrigendum to “Development of N-2,4-pyrimidine- N-phenyl- N′-phenyl ureas as inhibitors of tumor necrosis factor alpha (TNF-α) synthesis. Part 1” [Bioorg. Med. Chem. Lett. 16 (2006) 3510–3513]

The Development of Novel Inhibitors of Tumor Necrosis Factor-α (TNF-α) Production Based on Substituted [5,5]-Bicyclic Pyrazolones

Synthesis of Novel Pyrimido[4,5-c]pyridazines and 1,2-Dihydro-3a,7,9,9b-tetraaza-cyclopenta[a]naphthalen-3-ones as Potent Inhibitors of Lymphocyte Specific Kinase (LCK)

ChemInform Abstract: Chemoenzymatic Synthesis of Functionalized Cyclohexylglycines and α-Methylcyclohexylglycines via Kazmaier-Claisen Rearrangement

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