Design and synthesis of dihydroindazolo[5,4-a]pyrrolo[3,4-c]carbazole oximes as potent dual inhibitors of TIE-2 and VEGF-R2 receptor tyrosine kinases. [electronic resource]
Producer: 20080609Description: 1916-21 p. digitalISSN:- 1464-3405
- Administration, Oral
- Angiogenesis Inhibitors -- chemical synthesis
- Animals
- Cell Proliferation -- drug effects
- Cells, Cultured
- Drug Design
- Endothelium, Vascular -- cytology
- Hemangiosarcoma -- blood supply
- Humans
- Melanoma, Experimental -- blood
- Molecular Structure
- Neovascularization, Pathologic
- Oximes -- chemical synthesis
- Protein Kinase Inhibitors -- chemical synthesis
- Rats
- Receptor, TIE-2 -- antagonists & inhibitors
- Structure-Activity Relationship
- Umbilical Veins
- Vascular Endothelial Growth Factor Receptor-2 -- antagonists & inhibitors
No physical items for this record
Publication Type: Journal Article
There are no comments on this title.
Log in to your account to post a comment.