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TitleDesign and synthesis of novel benzimidazole derivatives as phosphodiesterase 10A inhibitors with reduced CYP1A2 inhibition.
Journal, issue, pagesBioorg. Med. Chem., Vol. 21, Page 7612-7623, Year 2013
Publish dateSep 4, 2013 (structure data deposition date)
AuthorsHamaguchi, W. / Masuda, N. / Isomura, M. / Miyamoto, S. / Kikuchi, S. / Amano, Y. / Honbou, K. / Mihara, T. / Watanabe, T.
External linksBioorg. Med. Chem. / PubMed:24238902
MethodsX-ray diffraction
Resolution2.26 Å
Structure data

PDB-3wi2:
Crystal structure of PDE10A in complex with inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.26 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-MG:
Unknown entry

ChemComp-P98:
2-({[1-phenyl-2-(propan-2-yl)-1H-benzimidazol-6-yl]oxy}methyl)quinoline

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / phosphodiesterase / cGMP binding / HYDROLASE-HYDROLASE INHIBITOR complex

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