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Titlep38alpha mitogen-activated protein kinase inhibitors: optimization of a series of biphenylamides to give a molecule suitable for clinical progression.
Journal, issue, pagesJ. Med. Chem., Vol. 52, Page 6257-6269, Year 2009
Publish dateAug 17, 2009 (structure data deposition date)
AuthorsAston, N.M. / Bamborough, P. / Buckton, J.B. / Edwards, C.D. / Holmes, D.S. / Jones, K.L. / Patel, V.K. / Smee, P.A. / Somers, D.O. / Vitulli, G. / Walker, A.L.
External linksJ. Med. Chem. / PubMed:19772287
MethodsX-ray diffraction
Resolution2.1 Å
Structure data

PDB-3iph:
Crystal structure of p38 in complex with a biphenylamide inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

Chemicals

ChemComp-G11:
6-[5-(cyclopropylcarbamoyl)-2-methylphenyl]-N-(cyclopropylmethyl)pyridine-3-carboxamide

ChemComp-SO4:
SULFATE ION

ChemComp-GOL:
GLYCEROL

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / P38 / SERINE/THREONINE PROTEIN KINASE / MAP KINASE / ATP-binding / Kinase / Nucleotide-binding / Nucleus / Phosphoprotein / Serine/threonine-protein kinase

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