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Improving therapeutic synergy score predictions with adverse effects using multi-task heterogeneous network learning

Briefings in bioinformatics, 2023-01, Vol.24 (1)

2023

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α-Tocopherol Pharmacokinetics in Adults with Cystic Fibrosis: Benefits of Supplemental Vitamin C Administration

Nutrients, 2022-09, Vol.14 (18), p.3717

2022

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Cobdock: an accurate and practical machine learning-based consensus blind docking method

Journal of cheminformatics, 2024-01, Vol.16 (1), p.5-5, Article 5

2024

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Identification of NVP-TNKS656: The Use of Structure–Efficiency Relationships To Generate a Highly Potent, Selective, and Orally Active Tankyrase Inhibitor

Journal of medicinal chemistry, 2013-08, Vol.56 (16), p.6495-6511

2013

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1-Amino-4-benzylphthalazines as Orally Bioavailable Smoothened Antagonists with Antitumor Activity

Journal of medicinal chemistry, 2009-07, Vol.52 (13), p.3954-3968

2009

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Optimization of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidine IGF-1R tyrosine kinase inhibitors towards JNK selectivity

Bioorganic & medicinal chemistry letters, 2009-01, Vol.19 (2), p.360-364

2009

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Discovery of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidines : Potent inhibitors of the IGF-1R receptor tyrosine kinase

Bioorganic & medicinal chemistry letters, 2009-01, Vol.19 (2), p.469-473

2009

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Optimization of a series of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidine inhibitors of IGF-1R : Elimination of an acid-mediated decomposition pathway

Bioorganic & medicinal chemistry letters, 2009-01, Vol.19 (2), p.373-377

2009

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Reversible Carboxamide-Mediated Internal Activation at C(6) of 2-Chloro-4-anilino-1H-pyrrolo[2,3-d]pyrimidines

Journal of organic chemistry, 2008-12, Vol.73 (23), p.9511-9514

2008

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FLONE: fully Lorentz network embedding for inferring novel drug targets

Bioinformatics advances, 2023, Vol.3 (1), p.vbad066-vbad066

2023

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The design and synthesis of human branched-chain amino acid aminotransferase inhibitors for treatment of neurodegenerative diseases

Bioorganic & medicinal chemistry letters, 2006-05, Vol.16 (9), p.2337-2340

2006

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Hydrogen-deuterium exchange during the reductive deuteration of α- and γ-tocopherol chromenes

Journal of labelled compounds & radiopharmaceuticals, 2001-03, Vol.44 (3), p.215-223

2001

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Synthesis of photoaffinity label analogues of α-tocopherol

Bioorganic & medicinal chemistry letters, 1998-12, Vol.8 (24), p.3453-3458

1998

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Discovery of 3,5-disubstituted-1H-pyrrolo[2,3-b]pyridines as potent inhibitors of the insulin-like growth factor-1 receptor (IGF-1R) tyrosine kinase

Bioorganic & medicinal chemistry letters, 2009-06, Vol.19 (11), p.3136-3140

2009

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Reversible Carboxamide-Mediated Internal Activation at C(6) of 2-Chloro-4-anilino-1 H -pyrrolo[2,3- d ]pyrimidines

Journal of organic chemistry, 2008-12, Vol.73 (23), p.9511-9514

2008

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Synthesis of Phytyl- and Chroman-Derivatized Photoaffinity Labels Based on α-Tocopherol

Journal of organic chemistry, 2000-04, Vol.65 (8), p.2560-2567

2000

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Synthesis and biological evaluation of amino-pyridines as androgen receptor antagonists for stimulating hair growth and reducing sebum production

Bioorganic & medicinal chemistry letters, 2007-10, Vol.17 (20), p.5693-5697

2007

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The Mannich Reaction Between Aromatic Ketones, Aromatic Aldehydes and Aromatic Amines

Synthesis (Stuttgart), 1991, Vol.1991 (9), p.717-718

1991

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Discovery of 3,5-disubstituted-lH-pyrrolo[2,3-b]pyridines as potent inhibitors of the insulin-like growth factor-1 receptor (IGF-1R) tyrosine kinase

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (11), p.3136-3140

2009

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Optimization of a series of 4,6-bis-anilino-1 H-pyrrolo[2,3- d]pyrimidine inhibitors of IGF-1R: Elimination of an acid-mediated decomposition pathway

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (2), p.373-377

2009

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(1 R ,2 S )-4-(2-Cyano-cyclohexyl-oxy)-2-trifluoromethyl-benzonitrile, a potent androgen receptor antagonist for stimulating hair growth and reducing sebum production

Bioorganic & medicinal chemistry letters, 2007-11, Vol.17 (21), p.5983-5988

2007

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Discovery of 4,6-bis-anilino-1 H-pyrrolo[2,3- d]pyrimidines: Potent inhibitors of the IGF-1R receptor tyrosine kinase

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (2), p.469-473

2009

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Optimization of 4,6-bis-anilino-1 H-pyrrolo[2,3- d]pyrimidine IGF-1R tyrosine kinase inhibitors towards JNK selectivity

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (2), p.360-364

2009

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Optimization of 4,6-bis-anilmo-1H-pyrrolo[2,3-d]pyrimidme IGF-1R tyrosine kinase inhibitors towards JNK selectivity

Bioorganic & medicinal chemistry letters, 2009, Vol.19 (2), p.360-364

2009

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THE MANNICH REACTION OF CYCLIC KETONES, AROMATIC ALDEHYDES AND AROMATIC AMINES

Organic preparations and procedures international, 1991-10, Vol.23 (5), p.673-676

1991

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Improving therapeutic synergy score predictions with adverse effects using multi-task heterogeneous network learning

α-Tocopherol Pharmacokinetics in Adults with Cystic Fibrosis: Benefits of Supplemental Vitamin C Administration

Cobdock: an accurate and practical machine learning-based consensus blind docking method

Identification of NVP-TNKS656: The Use of Structure–Efficiency Relationships To Generate a Highly Potent, Selective, and Orally Active Tankyrase Inhibitor

1-Amino-4-benzylphthalazines as Orally Bioavailable Smoothened Antagonists with Antitumor Activity

Optimization of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidine IGF-1R tyrosine kinase inhibitors towards JNK selectivity

Discovery of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidines : Potent inhibitors of the IGF-1R receptor tyrosine kinase

Optimization of a series of 4,6-bis-anilino-1H-pyrrolo[2,3-d]pyrimidine inhibitors of IGF-1R : Elimination of an acid-mediated decomposition pathway

Reversible Carboxamide-Mediated Internal Activation at C(6) of 2-Chloro-4-anilino-1H-pyrrolo[2,3-d]pyrimidines

FLONE: fully Lorentz network embedding for inferring novel drug targets

The design and synthesis of human branched-chain amino acid aminotransferase inhibitors for treatment of neurodegenerative diseases

Hydrogen-deuterium exchange during the reductive deuteration of α- and γ-tocopherol chromenes

Synthesis of photoaffinity label analogues of α-tocopherol

Discovery of 3,5-disubstituted-1H-pyrrolo[2,3-b]pyridines as potent inhibitors of the insulin-like growth factor-1 receptor (IGF-1R) tyrosine kinase

Reversible Carboxamide-Mediated Internal Activation at C(6) of 2-Chloro-4-anilino-1 H -pyrrolo[2,3- d ]pyrimidines

Synthesis of Phytyl- and Chroman-Derivatized Photoaffinity Labels Based on α-Tocopherol

Synthesis and biological evaluation of amino-pyridines as androgen receptor antagonists for stimulating hair growth and reducing sebum production

The Mannich Reaction Between Aromatic Ketones, Aromatic Aldehydes and Aromatic Amines

Discovery of 3,5-disubstituted-lH-pyrrolo[2,3-b]pyridines as potent inhibitors of the insulin-like growth factor-1 receptor (IGF-1R) tyrosine kinase

Optimization of a series of 4,6-bis-anilino-1 H-pyrrolo[2,3- d]pyrimidine inhibitors of IGF-1R: Elimination of an acid-mediated decomposition pathway

(1 R ,2 S )-4-(2-Cyano-cyclohexyl-oxy)-2-trifluoromethyl-benzonitrile, a potent androgen receptor antagonist for stimulating hair growth and reducing sebum production

Discovery of 4,6-bis-anilino-1 H-pyrrolo[2,3- d]pyrimidines: Potent inhibitors of the IGF-1R receptor tyrosine kinase

Optimization of 4,6-bis-anilino-1 H-pyrrolo[2,3- d]pyrimidine IGF-1R tyrosine kinase inhibitors towards JNK selectivity

Optimization of 4,6-bis-anilmo-1H-pyrrolo[2,3-d]pyrimidme IGF-1R tyrosine kinase inhibitors towards JNK selectivity

THE MANNICH REACTION OF CYCLIC KETONES, AROMATIC ALDEHYDES AND AROMATIC AMINES

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