Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1370408 | Bioorganic & Medicinal Chemistry Letters | 2011 | 5 Pages |
Abstract
The co-crystal structure of the human acetyl-coenzyme A 2 (ACC2) carboxyl transferase domain and the reported compound CP-640186 (1b) suggested that two carbonyl groups are essential for potent ACC2 inhibition. By focusing on enhancing the interactions between the two carbonyl groups and the amino acid residues Gly2162 and Glu2230, we used ligand- and structure-based drug design to discover spirolactones bearing a 2-ureidobenzothiophene moiety
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tohru Yamashita, Makoto Kamata, Satoshi Endo, Mitsuo Yamamoto, Keiko Kakegawa, Hiroyuki Watanabe, Katsuhiko Miwa, Toru Yamano, Masaaki Funata, Jyun-ichi Sakamoto, Akiyoshi Tani, Clifford D. Mol, Hua Zou, Douglas R. Dougan, BiChing Sang, Gyorgy Snell,