Design and synthesis of novel 5-(3,4,5-trimethoxybenzoyl)-4-aminopyrimidine derivatives as potent and selective phosphodiesterase 5 inhibitors: Scaffold hopping using a pseudo-ring by intramolecular hydrogen bond formation
- 1 November 2014
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 24 (22) , 5175-5180
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Exploration of the 5-bromopyrimidin-4(3H)-ones as potent inhibitors of PDE5Bioorganic & Medicinal Chemistry Letters, 2013
- Synthesis of quinoline derivatives: Discovery of a potent and selective phosphodiesterase 5 inhibitor for the treatment of Alzheimer's diseaseEuropean Journal of Medicinal Chemistry, 2013
- Discovery of potent, selective, and orally bioavailable PDE5 inhibitor: Methyl-4-(3-chloro-4-methoxybenzylamino)-8-(2-hydroxyethyl)-7-methoxyquinazolin-6-ylmethylcarbamate (CKD 533)Bioorganic & Medicinal Chemistry Letters, 2010
- Optimization of the aminopyridopyrazinones class of PDE5 inhibitors: Discovery of 3-[(trans-4-hydroxycyclohexyl)amino]-7-(6-methoxypyridin-3-yl)-1-(2-propoxyethyl)pyrido[3,4-b]pyrazin-2(1H)-oneBioorganic & Medicinal Chemistry Letters, 2009
- Entry into a new class of protein kinase inhibitors by pseudo ring designBioorganic & Medicinal Chemistry Letters, 2008
- Scaffold hoppingDrug Discovery Today: Technologies, 2004
- Characteristics of Photoreceptor PDE (PDE6): similarities and differences to PDE5International Journal Of Impotence Research, 2004
- Identification of a new chemical class of potent angiogenesis inhibitors based on conformational considerations and database searchingBioorganic & Medicinal Chemistry Letters, 2003
- Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settingsAdvanced Drug Delivery Reviews, 1997
- Metelation of diazines VIII metalation of 4-chloropyrimidine derivatives new synthesis of trimethoprimTetrahedron Letters, 1993