✦ LIBER ✦

SAR of Benzoylpyridines and Benzophenones as p38α MAP Kinase Inhibitors with Oral Activity.

✍ Scribed by Laszlo Revesz; Ernst Blum; Franco E. Di Padova; Thomas Buhl; Roland Feifel; Hermann Gram; Peter Hiestand; Ute Manning; Gerard Rucklin

Publisher: John Wiley and Sons
Year: 2004
Weight: 15 KB
Volume: 35
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200443234

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Pyrazoloheteroaryls: Novel p38α MAP Kina

Pyrazoloheteroaryls: Novel p38α MAP Kinase Inhibiting Scaffolds with Oral Activity.

✍ Laszlo Revesz; Ernst Blum; Franco E. Di Padova; Thomas Buhl; Roland Feifel; Herm 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 25 KB

SAR of 2,6-Diamino-3,5-difluoropyridinyl

SAR of 2,6-Diamino-3,5-difluoropyridinyl Substituted Heterocycles as Novel p38 MAP Kinase Inhibitors

✍ Laszlo Revesz; Franco E. Di Padova; Thomas Buhl; Roland Feifel; Hermann Gram; Pe 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

ChemInform Abstract: SAR of 4-Hydroxypip

ChemInform Abstract: SAR of 4-Hydroxypiperidine and Hydroxyalkyl Substituted Heterocycles as Novel p38 Map Kinase Inhibitors.

✍ Laszlo Revesz; Franco E. Di Padova; Thomas Buhl; Roland Feifel; Hermann Gram; Pe 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

ChemInform Abstract: Substituted N-Aryl-

ChemInform Abstract: Substituted N-Aryl-6-pyrimidinones: A New Class of Potent, Selective, and Orally Active p38 MAP Kinase Inhibitors.

✍ Balekudru Devadas; et al. et al. 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 22 KB 👁 1 views

## Abstract A series of highly potent and selective p38 MAP kinase inhibitors is developed originating from a substituted N‐aryl‐6‐pyrimidinone scaffold.

Synthesis and Biological Activities of 4

Synthesis and Biological Activities of 4-Phenyl-5-pyridyl-1,3-thiazole Derivatives as p38 MAP Kinase Inhibitors.

✍ Seiji Miwatashi; Yasuyoshi Arikawa; Ken-ichi Naruo; Keiko Igaki; Yasumasa Watana 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 25 KB 👁 2 views

ChemInform Abstract: Design, Synthesis a

ChemInform Abstract: Design, Synthesis and SAR of Phenylamino-Substituted 5,11-Dihydrodibenzo[a,d]cyclohepten-10-ones and 11H-Dibenzo[b,f]oxepin-10-ones as p38 MAP Kinase Inhibitors.

✍ Angelika Dorn; Verena Schattel; Stefan Laufer 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views