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Design, Synthesis, and Activity of 2-Imidazol-1-ylpyrimidine Derived Inducible Nitric Oxide Synthase Dimerization Inhibitors

Journal of medicinal chemistry, 2007-03, Vol.50 (6), p.1146-1157

2007

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Identification and Characterization of a Potent, Selective, and Orally Active Antagonist of the CC Chemokine Receptor-1

The Journal of biological chemistry, 2000-06, Vol.275 (25), p.19000-19008

2000

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Thiophene-Anthranilamides as Highly Potent and Orally Available Factor Xa Inhibitors

Journal of medicinal chemistry, 2007-06, Vol.50 (13), p.2967-2980

2007

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An efficient approach to the azaspirocyclic structure of halichlorine and pinnaic acid

Tetrahedron letters, 1999-11, Vol.40 (45), p.7921-7924

1999

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Substituted thiophene-anthranilamides as potent inhibitors of human factor Xa

Bioorganic & medicinal chemistry, 2007-03, Vol.15 (5), p.2127-2146

2007

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Synthetic Studies on Halichlorine and Pinnaic Acid. Stereospecific Preparation of the Azaspiro Core Structure

Organic letters, 1999-08, Vol.1 (4), p.681-684

Lee, Sangku

1999

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Synthesis and biological evaluation of piperazine-based derivatives as inhibitors of plasminogen activator inhibitor-1 (PAI-1)

Bioorganic & medicinal chemistry letters, 2004-02, Vol.14 (3), p.761-765

2004

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Synthesis and biological evaluation of menthol-based derivatives as inhibitors of plasminogen activator inhibitor-1 (PAI-1)

Bioorganic & medicinal chemistry letters, 2003-10, Vol.13 (19), p.3361-3365

2003

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Crystallographic analysis of potent and selective factor Xa inhibitors complexed to bovine trypsin

Acta crystallographica. Section D, Biological crystallography., 1999-08, Vol.55 (8), p.1395-1404

1999

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Benzimidazole-Based fXa inhibitors with improved thrombin and trypsin selectivity

Bioorganic & medicinal chemistry letters, 2002-05, Vol.12 (9), p.1311-1314

2002

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Dehydroamino acid derivatives from D-arabinose and L-serine: synthesis of models for the azinomycin antitumor antibiotics

Journal of organic chemistry, 1993-12, Vol.58 (27), p.7848-7859

1993

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Synthesis of trans-4-alkenyl oxazoles

Tetrahedron letters, 1991-03, Vol.32 (13), p.1609-1612

1991

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Design and synthesis of aminophenol-Based factor xa inhibitors

Bioorganic & medicinal chemistry letters, 2002-05, Vol.12 (9), p.1307-1310

2002

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Tannins and other phenolics from Myrica esculenta bark

Phytochemistry (Oxford), 1988, Vol.27 (2), p.579-583

1988

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Design, synthesis, and in vitro biological activity of benzimidazole based factor Xa inhibitors

Bioorganic & medicinal chemistry letters, 2000-05, Vol.10 (9), p.963-966

2000

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Inhibition of PAI-1: a new anti-thrombotic approach

Current drug targets. Cardiovascular & hematological disorders, 2002-06, Vol.2 (1), p.27-42

2002

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Design, synthesis, and in vitro biological activity of indole-based factor Xa inhibitors

Bioorganic & medicinal chemistry letters, 2000-05, Vol.10 (9), p.957-961

2000

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Revision to the stereochemistry of ficellomycin and the first synthesis of fully protected deguanylated ficellomycin

Zhao, Zuchun

1993

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ChemInform Abstract: An Efficient Approach to the Azaspirocyclic Structure of Halichlorine and Pinnaic Acid

ChemInform, 2000-02, Vol.31 (5), p.no-no

2000

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ChemInform Abstract: Synthetic Studies on Halichlorine and Pinnaic Acid. Stereospecific Preparation of the Azaspiro Core Structure

ChemInform, 1999-12, Vol.30 (49), p.no-no

1999

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Synthesis and Biological Evaluation of Menthol-Based Derivatives as Inhibitors of Plasminogen Activator Inhibitor-1 (PAI-1)

ChemInform, 2004-01, Vol.35 (1), p.no-no

2004

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ChemInform Abstract: Design, Synthesis, and in vitro Biological Activity of Benzimidazole-Based Factor Xa Inhibitors

ChemInform, 2000-08, Vol.31 (35), p.no-no

2000

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ChemInform Abstract: Benzimidazole-Based fXa Inhibitors with Improved Thrombin and Trypsin Selectivity

ChemInform, 2002-08, Vol.33 (31), p.no-no

2002

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ChemInform Abstract: Design, Synthesis, and in Vitro Biological Activity of Indole-Based Factor Xa Inhibitors

ChemInform, 2000-08, Vol.31 (35), p.no-no

2000

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In Situ Construction of Crumpled Ti 3 C 2 T x Nanosheets Confined S-Doping Red Phosphorus by Ti-O-P Bonds for LIBs Anode with Enhanced Electrochemical Performance

ACS applied materials & interfaces, 2024-10, Vol.16 (39), p.52393-52405

2024

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Design, Synthesis, and Activity of 2-Imidazol-1-ylpyrimidine Derived Inducible Nitric Oxide Synthase Dimerization Inhibitors

Identification and Characterization of a Potent, Selective, and Orally Active Antagonist of the CC Chemokine Receptor-1

Thiophene-Anthranilamides as Highly Potent and Orally Available Factor Xa Inhibitors

An efficient approach to the azaspirocyclic structure of halichlorine and pinnaic acid

Substituted thiophene-anthranilamides as potent inhibitors of human factor Xa

Synthetic Studies on Halichlorine and Pinnaic Acid. Stereospecific Preparation of the Azaspiro Core Structure

Synthesis and biological evaluation of piperazine-based derivatives as inhibitors of plasminogen activator inhibitor-1 (PAI-1)

Synthesis and biological evaluation of menthol-based derivatives as inhibitors of plasminogen activator inhibitor-1 (PAI-1)

Crystallographic analysis of potent and selective factor Xa inhibitors complexed to bovine trypsin

Benzimidazole-Based fXa inhibitors with improved thrombin and trypsin selectivity

Dehydroamino acid derivatives from D-arabinose and L-serine: synthesis of models for the azinomycin antitumor antibiotics

Synthesis of trans-4-alkenyl oxazoles

Design and synthesis of aminophenol-Based factor xa inhibitors

Tannins and other phenolics from Myrica esculenta bark

Design, synthesis, and in vitro biological activity of benzimidazole based factor Xa inhibitors

Inhibition of PAI-1: a new anti-thrombotic approach

Design, synthesis, and in vitro biological activity of indole-based factor Xa inhibitors

Revision to the stereochemistry of ficellomycin and the first synthesis of fully protected deguanylated ficellomycin

ChemInform Abstract: An Efficient Approach to the Azaspirocyclic Structure of Halichlorine and Pinnaic Acid

ChemInform Abstract: Synthetic Studies on Halichlorine and Pinnaic Acid. Stereospecific Preparation of the Azaspiro Core Structure

Synthesis and Biological Evaluation of Menthol-Based Derivatives as Inhibitors of Plasminogen Activator Inhibitor-1 (PAI-1)

ChemInform Abstract: Design, Synthesis, and in vitro Biological Activity of Benzimidazole-Based Factor Xa Inhibitors

ChemInform Abstract: Benzimidazole-Based fXa Inhibitors with Improved Thrombin and Trypsin Selectivity

ChemInform Abstract: Design, Synthesis, and in Vitro Biological Activity of Indole-Based Factor Xa Inhibitors

In Situ Construction of Crumpled Ti 3 C 2 T x Nanosheets Confined S-Doping Red Phosphorus by Ti-O-P Bonds for LIBs Anode with Enhanced Electrochemical Performance

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