✦ LIBER ✦

ChemInform Abstract: 1-Arylalkyl-Substituted Anthracenones as Inhibitors of 12-Lipoxygenase Enzymes. Part 1. Structure—Activity Relationships of the Terminal Aryl Ring.

✍ Scribed by Klaus Mueller; Reinhold Altmann; Helge Prinz

Publisher: John Wiley and Sons
Year: 2010
Weight: 28 KB
Volume: 33
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200201254

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

📜 SIMILAR VOLUMES

ChemInform Abstract: 2-Arylalkyl-Substit

ChemInform Abstract: 2-Arylalkyl-Substituted Anthracenones as Inhibitors of 12-Lipoxygenase Enzymes. Part 2. Structure—Activity Relationships of the Linker Chain.

✍ Klaus Mueller; Reinhold Altmann; Helge Prinz 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB 👁 1 views

ChemInform Abstract: Antagonists of the

ChemInform Abstract: Antagonists of the Human CCR5 Receptor as Anti-HIV-1 Agents. Part 2. Structure—Activity Relationships for Substituted 2-Aryl-1-[N-(methyl)-N-(phenylsulfonyl)amino] -4-(piperidin-1-yl)butanes.

✍ Paul E. Finke; et al. et al. 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

ChemInform Abstract: Nicotinamide Deriva

ChemInform Abstract: Nicotinamide Derivatives as a New Class of Gastric H+/K+-ATPase Inhibitors. Part 1. Synthesis and Structure-Activity Relationships of N-Substituted 2-(Benzhydryl- and benzylsulfinyl)nicotinamides.

✍ H. TERAUCHI; A. TANITAME; K. TADA; K. NAKAMURA; Y. SETO; Y. NISHIKAWA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

Nicotinamide Derivatives as a New Class of Gastric H+/K+-ATPase Inhibitors. Part 1. Synthesis and Structure-Activity Relationships of N-Substituted 2-(Benzhydryl-and benzylsulfinyl)nicotinamides. -A series of title compounds, e.g. (IV), (VIII), (IX), and (X), is synthesized. Acid activation convert