Synthesis of selective SRPK-1 inhibitors: Novel tricyclic quinoxaline derivatives-Reference-Cited by-同舟云学术

Synthesis of selective SRPK-1 inhibitors: Novel tricyclic quinoxaline derivatives

Published:2005-07 Issue:13 Volume:15 Page:3241-3246
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Székelyhidi Zsolt,Pató János,Wáczek Frigyes,Bánhegyi Péter,Hegymegi-Barakonyi Bálint,Ero˝s Dániel,Mészáros György,Hollósy Ferenc,Hafenbradl Doris,Obert Sabine,Klebl Bert,Kéri György,O˝rfi László

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference12 articles.

1. Identification of SRPK1 and SRPK2 as the Major Cellular Protein Kinases Phosphorylating Hepatitis B Virus Core Protein

2. Quinoxalin-2-ones

3. Novel CCR1 antagonists with improved metabolic stability

4. Design, Synthesis, and Biological Evaluation of Analogues of the Antitumor Agent, 2-{4-[(7-Chloro-2-quinoxalinyl)oxy]phenoxy}propionic Acid (XK469)

5. Potent quinoxaline-Based inhibitors of PDGF receptor tyrosine kinase activity. Part 1: SAR Exploration and Effective Bioisosteric Replacement of a phenyl substituent

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