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1U6Q

Substituted 2-Naphthamadine inhibitors of Urokinase

Summary for 1U6Q
Entry DOI10.2210/pdb1u6q/pdb
Related1owd 1owe 1owh 1owi 1owj 1sqa
DescriptorUrokinase-type plasminogen activator, TRANS-6-(2-PHENYLCYCLOPROPYL)-NAPHTHALENE-2-CARBOXAMIDINE (2 entities in total)
Functional Keywordshydrolase
Biological sourceHomo sapiens (human)
Cellular locationSecreted: P00749
Total number of polymer chains1
Total formula weight27908.87
Authors
Bruncko, M.,McClellan, W.,Wendt, M.D.,Sauer, D.R.,Geyer, A.,Dalton, C.R.,Kaminski, M.K.,Nienaber, V.L.,Rockway, T.R.,Giranda, V.L. (deposition date: 2004-07-30, release date: 2004-10-19, Last modification date: 2011-07-13)
Primary citationBruncko, M.,McClellan, W.J.,Wendt, M.D.,Sauer, D.R.,Geyer, A.,Dalton, C.R.,Kaminski, M.A.,Weitzberg, M.,Gong, J.,Dellaria, J.F.,Mantei, R.,Zhao, X.,Nienaber, V.L.,Stewart, K.,Klinghofer, V.,Bouska, J.,Rockway, T.W.,Giranda, V.L.
Naphthamidine urokinase plasminogen activator inhibitors with improved pharmacokinetic properties.
Bioorg.Med.Chem.Lett., 15:93-98, 2005
Cited by
PubMed: 15582418
DOI: 10.1016/j.bmcl.2004.10.026
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.02 Å)
Structure validation

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