000 02471nam a22005535i 4500
001 978-3-642-17969-3
003 DE-He213
005 20140220083752.0
007 cr nn 008mamaa
008 110621s2011 gw | s |||| 0|eng d
020 _a9783642179693
_9978-3-642-17969-3
024 7 _a10.1007/978-3-642-17969-3
_2doi
050 4 _aRM1-950
072 7 _aMMG
_2bicssc
072 7 _aMED071000
_2bisacsh
082 0 4 _a615
_223
100 1 _aFrancis, Sharron H.
_eeditor.
245 1 0 _aPhosphodiesterases as Drug Targets
_h[electronic resource] /
_cedited by Sharron H. Francis, Marco Conti, Miles D. Houslay.
264 1 _aBerlin, Heidelberg :
_bSpringer Berlin Heidelberg,
_c2011.
300 _aXVIII, 522 p.
_bonline resource.
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
347 _atext file
_bPDF
_2rda
490 1 _aHandbook of Experimental Pharmacology,
_x0171-2004 ;
_v204
520 _aCyclic nucleotide phosphodiesterases (PDEs) are promising targets for pharmacological intervention. Multiple PDE genes, isoform diversity, selective expression and compartmentation of the isoforms, and an array of conformations of PDE proteins are properties that challenge development of drugs that selectively target this class of enzymes. Novel characteristics of PDEs are viewed as unique opportunities to increase specificity and selectivity when designing novel compounds for certain therapeutic indications. This chapter provides a summary of the major concepts related to the design and use of PDE inhibitors.
650 0 _aMedicine.
650 0 _aToxicology.
650 0 _aBiochemistry.
650 0 _aEnzymes.
650 0 _aPost-translational modification of proteins.
650 0 _aCytology.
650 1 4 _aBiomedicine.
650 2 4 _aPharmacology/Toxicology.
650 2 4 _aMedicinal Chemistry.
650 2 4 _aProtein Structure.
650 2 4 _aEnzymology.
650 2 4 _aPosttranslational Modification.
650 2 4 _aCell Physiology.
700 1 _aConti, Marco.
_eeditor.
700 1 _aHouslay, Miles D.
_eeditor.
710 2 _aSpringerLink (Online service)
773 0 _tSpringer eBooks
776 0 8 _iPrinted edition:
_z9783642179686
830 0 _aHandbook of Experimental Pharmacology,
_x0171-2004 ;
_v204
856 4 0 _uhttp://dx.doi.org/10.1007/978-3-642-17969-3
912 _aZDB-2-SBL
999 _c107339
_d107339