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TitleHighly selective c-Jun N-terminal kinase (JNK) 2 and 3 inhibitors with in vitro CNS-like pharmacokinetic properties prevent neurodegeneration.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 21, Page 315-319, Year 2011
Publish dateSep 22, 2010 (structure data deposition date)
AuthorsProbst, G.D. / Bowers, S. / Sealy, J.M. / Truong, A.P. / Hom, R.K. / Galemmo, R.A. / Konradi, A.W. / Sham, H.L. / Quincy, D.A. / Pan, H. ...Probst, G.D. / Bowers, S. / Sealy, J.M. / Truong, A.P. / Hom, R.K. / Galemmo, R.A. / Konradi, A.W. / Sham, H.L. / Quincy, D.A. / Pan, H. / Yao, N. / Lin, M. / Toth, G. / Artis, D.R. / Zmolek, W. / Wong, K. / Qin, A. / Lorentzen, C. / Nakamura, D.F. / Quinn, K.P. / Sauer, J.M. / Powell, K. / Ruslim, L. / Wright, S. / Chereau, D. / Ren, Z. / Anderson, J.P. / Bard, F. / Yednock, T.A. / Griswold-Prenner, I.
External linksBioorg. Med. Chem. Lett. / PubMed:21112785
MethodsX-ray diffraction
Resolution1.7 Å
Structure data

PDB-3oy1:
Highly Selective c-Jun N-Terminal Kinase (JNK) 2 and 3 Inhibitors with In Vitro CNS-like Pharmacokinetic Properties
Method: X-RAY DIFFRACTION / Resolution: 1.7 Å

Chemicals

ChemComp-589:
5-[2-(cyclohexylamino)pyridin-4-yl]-4-naphthalen-2-yl-2-(tetrahydro-2H-pyran-4-yl)-2,4-dihydro-3H-1,2,4-triazol-3-one

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
Keywordstransherase/transferase inhibitor / Kinase inhibitor / CNS / Selectivity / TRANSFERASE / transherase-transferase inhibitor complex

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