✦ LIBER ✦

Substituted Benzylamino-6-(trifluoromethyl)pyrimidin-4(1H)-ones: A Novel Class of Selective Human A-FABP Inhibitors.

✍ Scribed by Rune Ringom; Eva Axen; Jonas Uppenberg; Thomas Lundbaeck; Lena Rondahl; Tjeerd Barf

Publisher: John Wiley and Sons
Year: 2004
Weight: 14 KB
Volume: 35
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200452135

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

📜 SIMILAR VOLUMES

6-Alkyl, Alkoxy, or Alkylthio-Substitute

6-Alkyl, Alkoxy, or Alkylthio-Substituted 3-(4-Methanesulfonylphenyl)-4-phenylpyran-2-ones: A Novel Class of Diarylheterocyclic Selective Cyclooxygenase-2 Inhibitors

✍ P. N. Praveen Rao; Mohsen Amini; Huiying Li; Amgad G. Habeeb; Edward E. Knaus 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 76 KB 👁 1 views

ChemInform Abstract: N-1 Substituted Pyr

ChemInform Abstract: N-1 Substituted Pyrimidin-4-ones: Novel, Orally Active Inhibitors of Lipoprotein-Associated Phospholipase A2.

✍ Stephen A. Smith; et al. et al. 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

ChemInform Abstract: Discovery of 1,6-Na

ChemInform Abstract: Discovery of 1,6-Naphthyridines as a Novel Class of Potent and Selective Human Cytomegalovirus Inhibitors.

✍ Laval Chan; Haolun Jin; Tomislav Stefanac; Jean-Francois Lavallee; Guy Falardeau 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 2 views

Discovery of 1,6-Naphthyridines as a Novel Class of Potent and Selective Human Cytomegalovirus Inhibitors. -A series of 20 1,6-naphthyridines, e.g. (I), is synthesized by amidation of key intermediate (IV) and in case of its halogen analogue (V) by subsequent Stille coupling with stannanes, e.g. (V

A Selective Synthesis of 3,6-Dihydro-7H-

A Selective Synthesis of 3,6-Dihydro-7H-1,2,3-triazolo[4,5-d]pyrimidin-7-ones.

✍ Jun-Feng Zhao; Chang Xie; Ming-Wu Ding; Hong-Wu He 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 18 KB 👁 1 views

Novel 3,4-Dihydroquinolin-2(1H)-one Inhi

Novel 3,4-Dihydroquinolin-2(1H)-one Inhibitors of Human Glycogen Phosphorylase a.

✍ Keith G. Rosauer; Anthony K. Ogawa; Chris A. Willoughby; Kenneth P. Ellsworth; W 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 83 KB 👁 1 views

ChemInform Abstract: Benzo[c]quinolizin-

ChemInform Abstract: Benzo[c]quinolizin-3-ones: A Novel Class of Potent and Selective Nonsteroidal Inhibitors of Human Steroid 5α-Reductase 1.

✍ Antonio Guarna; Fabrizio Machetti; Ernesto G. Occhiato; Dina Scarpi; Alessandra 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views