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-Structure paper
Title | Synthesis, SAR study, and biological evaluation of novel quinoline derivatives as phosphodiesterase 10A inhibitors with reduced CYP3A4 inhibition. |
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Journal, issue, pages | Bioorg. Med. Chem., Vol. 23, Page 297-313, Year 2015 |
Publish date | Oct 10, 2014 (structure data deposition date) |
Authors | Hamaguchi, W. / Masuda, N. / Miyamoto, S. / Shiina, Y. / Kikuchi, S. / Mihara, T. / Moriguchi, H. / Fushiki, H. / Murakami, Y. / Amano, Y. ...Hamaguchi, W. / Masuda, N. / Miyamoto, S. / Shiina, Y. / Kikuchi, S. / Mihara, T. / Moriguchi, H. / Fushiki, H. / Murakami, Y. / Amano, Y. / Honbou, K. / Hattori, K. |
External links | Bioorg. Med. Chem. / PubMed:25515954 |
Methods | X-ray diffraction |
Resolution | 3.13 Å |
Structure data | PDB-4wn1: |
Chemicals | ChemComp-ZN: ChemComp-MG: ChemComp-3SJ: ChemComp-HOH: |
Source |
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Keywords | HYDROLASE/HYDROLASE INHIBITOR / Phosphodiesterase / Complex / Inhibitor / HYDROLASE-HYDROLASE INHIBITOR complex |