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2OF2

crystal structure of furanopyrimidine 8 bound to lck

Summary for 2OF2
Entry DOI10.2210/pdb2of2/pdb
Related2OF4
DescriptorProto-oncogene tyrosine-protein kinase LCK, 2,3-DIPHENYL-N-(2-PIPERAZIN-1-YLETHYL)FURO[2,3-B]PYRIDIN-4-AMINE (3 entities in total)
Functional Keywordslck, kinase domain, transferase
Biological sourceHomo sapiens (human)
Cellular locationCytoplasm: P06239
Total number of polymer chains1
Total formula weight31744.39
Authors
Martin, M.W. (deposition date: 2007-01-02, release date: 2007-02-27, Last modification date: 2023-08-30)
Primary citationMartin, M.W.,Newcomb, J.,Nunes, J.J.,Bemis, J.E.,McGowan, D.C.,White, R.D.,Buchanan, J.L.,Dimauro, E.F.,Boucher, C.,Faust, T.,Hsieh, F.,Huang, X.,Lee, J.H.,Schneider, S.,Turci, S.M.,Zhu, X.
Discovery of novel 2,3-diarylfuro[2,3-b]pyridin-4-amines as potent and selective inhibitors of Lck: Synthesis, SAR, and pharmacokinetic properties.
Bioorg.Med.Chem.Lett., 17:2299-2304, 2007
Cited by
PubMed: 17276681
DOI: 10.1016/j.bmcl.2007.01.048
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

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