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Title | Furo[3,2-b]pyridine: A Privileged Scaffold for Highly Selective Kinase Inhibitors and Effective Modulators of the Hedgehog Pathway. |
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Journal, issue, pages | Angew. Chem. Int. Ed. Engl., Vol. 58, Page 1062-1066, Year 2019 |
Publish date | Nov 13, 2018 (structure data deposition date) |
![]() | Nemec, V. / Hylsova, M. / Maier, L. / Flegel, J. / Sievers, S. / Ziegler, S. / Schroder, M. / Berger, B.T. / Chaikuad, A. / Valcikova, B. ...Nemec, V. / Hylsova, M. / Maier, L. / Flegel, J. / Sievers, S. / Ziegler, S. / Schroder, M. / Berger, B.T. / Chaikuad, A. / Valcikova, B. / Uldrijan, S. / Drapela, S. / Soucek, K. / Waldmann, H. / Knapp, S. / Paruch, K. |
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Methods | X-ray diffraction |
Resolution | 1.49 - 2.55 Å |
Structure data | ![]() PDB-6i5h: ![]() PDB-6i5i: ![]() PDB-6i5k: ![]() PDB-6i5l: |
Chemicals | ![]() ChemComp-EDO: ![]() ChemComp-GOL: ![]() ChemComp-H3N: ![]() ChemComp-HOH: ![]() ChemComp-H3E: ![]() ChemComp-H3H: ![]() ChemComp-PO4: ![]() ChemComp-H3Q: |
Source |
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![]() | TRANSFERASE / PROTEIN TYROSINE KINASE / DUAL SPECIFICITY / SPLICING / HUMAN / Inhibitor / Structural Genomics / Structural Genomics Consortium / SGC / splicing kinase / furopyridine / CLK |