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TitleBenzimidazolone as potent chymase inhibitor: Modulation of reactive metabolite formation in the hydrophobic (P(1)) region.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 21, Page 4533-4539, Year 2011
Publish dateMay 13, 2011 (structure data deposition date)
AuthorsLo, H.Y. / Nemoto, P.A. / Kim, J.M. / Hao, M.H. / Qian, K.C. / Farrow, N.A. / Albaugh, D.R. / Fowler, D.M. / Schneiderman, R.D. / Michael August, E. ...Lo, H.Y. / Nemoto, P.A. / Kim, J.M. / Hao, M.H. / Qian, K.C. / Farrow, N.A. / Albaugh, D.R. / Fowler, D.M. / Schneiderman, R.D. / Michael August, E. / Martin, L. / Hill-Drzewi, M. / Pullen, S.S. / Takahashi, H. / De Lombaert, S.
External linksBioorg. Med. Chem. Lett. / PubMed:21733690
MethodsX-ray diffraction
Resolution1.95 Å
Structure data

PDB-3s0n:
Crystal Structure of Human Chymase with Benzimidazolone Inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.95 Å

Chemicals

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

ChemComp-ZN:
Unknown entry

ChemComp-0BB:
4-{3-[(4-methyl-1-benzothiophen-3-yl)methyl]-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl}butanoic acid

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE/HYDROLASE INHIBITOR / SERINE PROTEASE / HYDROLASE-HYDROLASE INHIBITOR complex

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