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Structure paper

TitleStructure-Based Library Design and the Discovery of a Potent and Selective Mast Cell Beta-Tryptase Inhibitor as an Oral Therapeutic Agent.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 22, Page 1049-, Year 2012
Publish dateNov 4, 2011 (structure data deposition date)
AuthorsLiang, G. / Aldous, S. / Merriman, G. / Levell, J. / Pribish, J. / Cairns, J. / Chen, X. / Maignan, S. / Mathieu, M. / Tsay, J. ...Liang, G. / Aldous, S. / Merriman, G. / Levell, J. / Pribish, J. / Cairns, J. / Chen, X. / Maignan, S. / Mathieu, M. / Tsay, J. / Sides, K. / Rebello, S. / Whitely, B. / Morize, I. / Pauls, H.W.
External linksBioorg. Med. Chem. Lett. / PubMed:22192588
MethodsX-ray diffraction
Resolution2.05 Å
Structure data

PDB-4a6l:
beta-tryptase inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.05 Å

Chemicals

ChemComp-P43:
1-{3-[1-({5-[(2-fluorophenyl)ethynyl]furan-2-yl}carbonyl)piperidin-4-yl]phenyl}methanamine

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsHYDROLASE / INHIBITOR

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