5-Lipoxygenase inhibitors: convenient synthesis of 4-[3-(4-heterocyclylphenylthio)phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxamide analogues-Reference-Cited by-同舟云学术

5-Lipoxygenase inhibitors: convenient synthesis of 4-[3-(4-heterocyclylphenylthio)phenyl]-3,4,5,6-tetrahydro-2H-pyran-4-carboxamide analogues

Published:2005-05 Issue:10 Volume:15 Page:2611-2615
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Mano Takashi,Stevens Rodney W.,Okumura Yoshiyuki,Kawai Makoto,Okumura Takako,Sakakibara Minoru

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference12 articles.

1. Novel imidazole compounds as a new series of potent, orally active inhibitors of 5-lipoxygenase

2. 4-[5-Fluoro-3-[4-(2-methyl-1H-imidazol-1-yl)benzyloxy]phenyl]-3,4,5,6- tetrahydro-2H-pyran-4-carboxamide, an Orally Active Inhibitor of 5-Lipoxygenase with Improved Pharmacokinetic and Toxicology Characteristics

3. Mano, T.; Stevens, R. W.; Ando, K.; Kawamura, K.; Nakao, K.; Okumura, Y.; Okumura, T.; Sakakibara, M.; Miyamoto, K.; Tamura; T. Eur. J. Med. Chem., in press

4. Nickel(0)-catalyzed Synthesis of Diaryl Sulfides from Aryl Halides and Aromatic Thiols

5. Stereochemistry of 5-Co-ordinated Compounds. III. Some New Phosphine Complexes of Divalent Nickel and Cobalt.

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