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TitleFused bicyclic heteroarylpiperazine-substituted l-prolylthiazolidines as highly potent DPP-4 inhibitors lacking the electrophilic nitrile group
Journal, issue, pagesBioorg. Med. Chem., Vol. 20, Page 5033-5041, Year 2012
Publish dateOct 24, 2011 (structure data deposition date)
AuthorsYoshida, T. / Akahoshi, F. / Sakashita, H. / Sonda, S. / Takeuchi, M. / Tanaka, Y. / Nabeno, M. / Kishida, H. / Miyaguchi, I. / Hayashi, Y.
External linksBioorg. Med. Chem. / PubMed:22824762
MethodsX-ray diffraction
Resolution2.1 Å
Structure data

PDB-3vjm:
Crystal structure of human depiptidyl peptidase IV (DPP-4) in complex with a prolylthiazolidine inhibitor #1
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

Chemicals

ChemComp-W61:
1,3-thiazolidin-3-yl[(2S,4S)-4-{4-[2-(trifluoromethyl)quinolin-4-yl]piperazin-1-yl}pyrrolidin-2-yl]methanone

ChemComp-NAG:
2-acetamido-2-deoxy-beta-D-glucopyranose

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / ALPHA/BETA / BETA-PROPELLER / AMINOPEPTIDASE / SERINE PROTEASE / SIGNAL-ANCHOR / TRANSMEMBRANE / DIABETES / GLYCOPROTEIN / CELL MEMBRANE / HYDROLASE-HYDROLASE INHIBITOR complex

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