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Structure paper

TitleDesign and synthesis of a pyrido[2,3-d]pyrimidin-5-one class of anti-inflammatory FMS inhibitors.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 18, Page 2355-2361, Year 2008
Publish dateNov 16, 2007 (structure data deposition date)
AuthorsHuang, H. / Hutta, D.A. / Hu, H. / DesJarlais, R.L. / Schubert, C. / Petrounia, I.P. / Chaikin, M.A. / Manthey, C.L. / Player, M.R.
External linksBioorg. Med. Chem. Lett. / PubMed:18342505
MethodsX-ray diffraction
Resolution2.02 Å
Structure data

PDB-3bea:
cFMS tyrosine kinase (tie2 KID) in complex with a pyrimidinopyridone inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.02 Å

Chemicals

ChemComp-SO4:
SULFATE ION

ChemComp-IXH:
8-(2,3-dihydro-1H-inden-5-yl)-2-({4-[(3R,5S)-3,5-dimethylpiperazin-1-yl]phenyl}amino)-5-oxo-5,8-dihydropyrido[2,3-d]pyrimidine-6-carboxamide

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / Kinase domain / inhibitor / juxtamembrane domain / ATP-binding / Glycoprotein / Immunoglobulin domain / Nucleotide-binding / Phosphoprotein / Polymorphism / Proto-oncogene / Receptor / Transmembrane / Tyrosine-protein kinase

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