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TitleDesign, Synthesis, and Evaluation of 2-Methyl- and 2-Amino-N-Aryl-4,5-Dihydrothiazolo[4,5-H]Quinazolin-8-Amines as Ring-Constrained 2-Anilino-4-(Thiazol-5-Yl)Pyrimidine Cyclin-Dependent Kinase Inhibitors.
Journal, issue, pagesJ. Med. Chem., Vol. 53, Page 2136-, Year 2010
Publish dateDec 31, 2009 (structure data deposition date)
AuthorsMcintyre, N.A. / Mcinnes, C. / Griffiths, G. / Barnett, A.L. / Kontopidis, G. / Slawin, A.M.Z. / Jackson, W. / Thomas, M. / Zheleva, D.I. / Wang, S. ...Mcintyre, N.A. / Mcinnes, C. / Griffiths, G. / Barnett, A.L. / Kontopidis, G. / Slawin, A.M.Z. / Jackson, W. / Thomas, M. / Zheleva, D.I. / Wang, S. / Blake, D.G. / Westwood, N.J. / Fischer, P.M.
External linksJ. Med. Chem. / PubMed:20146435
MethodsX-ray diffraction
Resolution2.75 Å
Structure data

PDB-2x1n:
Truncation and Optimisation of Peptide Inhibitors of CDK2, Cyclin A Through Structure Guided Design
Method: X-RAY DIFFRACTION / Resolution: 2.75 Å

Chemicals

ChemComp-X1N:
2-METHYL-N-[(1Z)-3-NITROCYCLOHEXA-2,4-DIEN-1-YLIDENE]-4,5-DIHYDRO[1,3]THIAZOLO[4,5-H]QUINAZOLIN-8-AMINE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
  • synthetic construct (others)
KeywordsCELL CYCLE / INHIBITION / TRANSFERASE / SERINE/THREONINE-PROTEIN KINASE / CELL DIVISION

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