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Synthesis & Biological Investigation of Fluorinated Amino Acid Analogs: Novel Amino Acid-based Molecules and Their Fluorinated Derivatives That May Bind Specifically to the 5/1 Integrin Ayse Demir
Synthesis & Biological Investigation of Fluorinated Amino Acid Analogs: Novel Amino Acid-based Molecules and Their Fluorinated Derivatives That May Bind Specifically to the 5/1 Integrin
Ayse Demir
Integrins are cell surface receptors that take part in cell ? cell adhesion and cell ? extracellular matrix (ECM) adhesion events as well as in cell migration and cell signaling. ?5?1 integrins are expressed on a wide range among brain tumor cells. In this study, an intermediate spiroisoxazolinopyrrole of the most specific ?5?1 integrin antagonist SJ749 was synthesized. Fischer esterification reaction, Swern oxidation, and Wittig olefination were performed. Next, fluorinated diaminopropionate molecules were synthesized for coupling to SJ749 instead of the (2,4,6-trimethylphenyl) diaminopropionate. Finally, the biological evaluation of the molecules synthesized was performed. These assays included cytotoxicity and cell proliferation.
| Medios de comunicación | Libros Paperback Book (Libro con tapa blanda y lomo encolado) |
| Publicado | 2 de febrero de 2012 |
| ISBN13 | 9783847348344 |
| Editores | LAP LAMBERT Academic Publishing |
| Páginas | 100 |
| Dimensiones | 150 × 6 × 226 mm · 167 g |
| Lengua | Alemán |
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