Phosphodiesterases as Drug Targets

• Συγγραφή απο Οργανισμό/Αρχή: SpringerLink (Online service)
• Άλλοι συγγραφείς: Francis, Sharron H. (Επιμελητής έκδοσης), Conti, Marco (Επιμελητής έκδοσης), Houslay, Miles D. (Επιμελητής έκδοσης)
• Μορφή: Ηλεκτρονική πηγή Ηλ. βιβλίο
• Γλώσσα: English
• Έκδοση: Berlin, Heidelberg : Springer Berlin Heidelberg, 2011.
• Σειρά: Handbook of Experimental Pharmacology, 204
• Θέματα: Medicine.; Pharmacology.; Medicinal chemistry.; Proteins.; Enzymology.; Posttranslational modification.; Cell physiology.; Biomedicine.; Pharmacology/Toxicology.; Medicinal Chemistry.; Protein Structure.; Posttranslational Modification.; Cell Physiology.
• Φυσική περιγραφή: XVIII, 522 p. online resource.
• ISBN: 9783642179693
• ISSN: 0171-2004 ;

Cyclic 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.