✦ LIBER ✦

Synthesis and Quantitative Structure−Activity Relationship of Fatty Acid Amide Hydrolase Inhibitors: Modulation at the N-Portion of Biphenyl-3-yl Alkylcarbamates

✍ Scribed by Mor, Marco; Lodola, Alessio; Rivara, Silvia; Vacondio, Federica; Duranti, Andrea; Tontini, Andrea; Sanchini, Silvano; Piersanti, Giovanni; Clapper, Jason R.; King, Alvin R.; Tarzia, Giorgio; Piomelli, Daniele

Book ID: 127344025
Publisher: American Chemical Society
Year: 2008
Tongue: English
Weight: 884 KB
Volume: 51
Category: Article
ISSN: 0022-2623
DOI: 10.1021/jm701631z

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and Quantitative Structure−Act

Synthesis and Quantitative Structure−Activity Relationship of Fatty Acid Amide Hydrolase Inhibitors: Modulation at the N-Portion of Biphenyl-3-yl Alkylcarbamates

✍ Mor, Marco; Lodola, Alessio; Rivara, Silvia; Vacondio, Federica; Duranti, Andrea 📂 Article 📅 2009 🏛 American Chemical Society 🌐 English ⚖ 19 KB

Synthesis and Structure–Activity Relatio

Synthesis and Structure–Activity Relationship Studies of O -Biphenyl-3-yl Carbamates as Peripherally Restricted Fatty Acid Amide Hydrolase Inhibitors

✍ Moreno-Sanz, Guillermo; Duranti, Andrea; Melzig, Laurin; Fiorelli, Claudio; Ruda 📂 Article 📅 2013 🏛 American Chemical Society 🌐 English ⚖ 850 KB

Cyclohexylcarbamic Acid 3‘- or 4‘-Substi

Cyclohexylcarbamic Acid 3‘- or 4‘-Substituted Biphenyl-3-yl Esters as Fatty Acid Amide Hydrolase Inhibitors: Synthesis, Quantitative Structure−Activity Relationships, and Molecular Modeling Studies

✍ Mor, Marco; Rivara, Silvia; Lodola, Alessio; Plazzi, Pier Vincenzo; Tarzia, Gior 📂 Article 📅 2004 🏛 American Chemical Society 🌐 English ⚖ 277 KB

Quantitative structure–activity relation

Quantitative structure–activity relationship study on the inhibitors of fatty acid amide hydrolase

✍ Peng Lu; Ruisheng Zhang; Yongna Yuan; Zhiguo Gong 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 345 KB 👁 2 views

## Abstract A quantitative structure activity relationship (QSAR) analysis was performed on the $K\_i $ values of a series of fatty acid amide hydrolase (FAAH) inhibitors. Six molecular descriptors selected by CODESSA software were used as inputs to perform heuristic method (HM) and support vector

Design, Synthesis, and Structure−Activit

Design, Synthesis, and Structure−Activity Relationships of Alkylcarbamic Acid Aryl Esters, a New Class of Fatty Acid Amide Hydrolase Inhibitors

✍ Tarzia, Giorgio; Duranti, Andrea; Tontini, Andrea; Piersanti, Giovanni; Mor, Mar 📂 Article 📅 2003 🏛 American Chemical Society 🌐 English ⚖ 189 KB

Biphenyl-3-yl alkylcarbamates as fatty a

Biphenyl-3-yl alkylcarbamates as fatty acid amide hydrolase (FAAH) inhibitors: Steric effects of N-alkyl chain on rat plasma and liver stability

✍ Federica Vacondio; Claudia Silva; Alessio Lodola; Caterina Carmi; Silvia Rivara; 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 693 KB