New pyrazolo[1',5':1,6]pyrimido[4,5-d]pyridazin-4(3H)-ones as potent and selective PDE5 inhibitors.
暂无分享,去创建一个
C. Vergelli | M. Giovannoni | V. Dal Piaz | A. Graziano | J. Feixas | Nicoletta Cesari | A. Gavaldà | V. Dal Piaz*
[1] H. Bergmeyer. Methods of Enzymatic Analysis , 2019 .
[2] Andrew Henwood,et al. Substituted pyrazolopyridopyridazines as orally bioavailable potent and selective PDE5 inhibitors: potential agents for treatment of erectile dysfunction. , 2003, Journal of medicinal chemistry.
[3] C. Gleiter,et al. Erectile dysfunction: comparison of efficacy and side effects of the PDE-5 inhibitors sildenafil, vardenafil and tadalafil--review of the literature. , 2002, European journal of medical research.
[4] J. Cartledge,et al. TADALAFIL (CIALIS™) FOR MEN WITH ERECTILE DYSFUNCTION , 2002, International journal of clinical practice.
[5] H. Porst. IC351 (tadalafil, Cialis): update on clinical experience , 2002, International Journal of Impotence Research.
[6] V. D. Piaz,et al. Synthesis and Evaluation of Some Pyrazolo[3,4-d]pyridazinones and Analogues as PDE 5 Inhibitors Potentially Useful as Peripheral Vasodilator Agents , 2002, Journal of enzyme inhibition and medicinal chemistry.
[7] M. Giovannoni,et al. Phosphodiesterase 4 inhibitors, structurally unrelated to rolipram, as promising agents for the treatment of asthma and other pathologies. , 2000, European journal of medicinal chemistry.
[8] G. Brock. Sildenafil citrate (Viagra). , 2000, Drugs of today.
[9] Aytaç,et al. The likely worldwide increase in erectile dysfunction between 1995 and 2025 and some possible policy consequences , 1999, BJU international.
[10] J. Corbin,et al. Cyclic GMP Phosphodiesterase-5: Target of Sildenafil* , 1999, The Journal of Biological Chemistry.
[11] V. D. Piaz,et al. Heterocyclic-fused 3(2H)-pyridazinones as potent and selective PDE IV inhibitors: Further structure-activity relationships and molecular modelling studies , 1998 .
[12] Truss Mc,et al. Phosphodiesterase inhibitors in the treatment of erectile dysfunction. , 1998 .
[13] M. Giovannoni,et al. Novel heterocyclic-fused pyridazinones as potent and selective phosphodiesterase IV inhibitors. , 1997, Journal of medicinal chemistry.
[14] Andrew Simon Bell,et al. Sildenafil (VIAGRATM), a potent and selective inhibitor of type 5 cGMP phosphodiesterase with utility for the treatment of male erectile dysfunction , 1996 .
[15] J. Beavo,et al. Cyclic nucleotide phosphodiesterases: functional implications of multiple isoforms. , 1995, Physiological reviews.
[16] J. Beavo,et al. Multiple cyclic nucleotide phosphodiesterases. , 1994, Molecular pharmacology.
[17] J. Beleta,et al. Studies on the cardiac actions of flosequinan in vitro , 1992, British journal of pharmacology.
[18] S. Pinzauti,et al. Condensation of some 3‐methylisoxazolo[3,4‐d]pyridazin‐7(6H)ones with aromatic aldehydes , 1976 .
[19] D. Juilfs,et al. Cyclic GMP as substrate and regulator of cyclic nucleotide phosphodiesterases (PDEs). , 1999, Reviews of physiology, biochemistry and pharmacology.
[20] J C Gingell,et al. The epidemiology and pathophysiology of erectile dysfunction. , 1999, The Journal of urology.
[21] M. Czarniecki,et al. Chapter 7. Inhibitors of Types I and V Phosphodiesterase: Elevation of cGMP as a Therapeutic Strategy , 1996 .
[22] K. Andersson,et al. Physiology of penile erection. , 1995, Physiological reviews.
[23] V. D. Piaz,et al. Pyrazolo[1',5':1,6]pyrimido[4,5-d]pyridazin-7(8H)-one: a new heterocyclic ring system from isoxazolopyridazinones , 1986 .