ChemInform Abstract: Stereospecific Synthesis of a Novel Farnesyl Protein Transferase Inhibitor, Valinoctin A and Its Analogues.
โ Scribed by M. TSUDA; Y. MURAOKA; T. TAKEUCHI; R. SEKIZAWA; K. UMEZAWA
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 30 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
โฆ Synopsis
Stereospecific Synthesis of a Novel Farnesyl Protein Transferase Inhibitor, Valinoctin A and Its Analogues.
-The valinoctin A analogue (VIII), prepared via Curtius rearrangement of an intermediate azide, shows essentially the same inhibitory activity as the parent compound. -
๐ SIMILAR VOLUMES
Novel Tricyclic Aminoacetyl and Sulfonamide Inhibitors of RAS Farnesyl Protein Transferase. -It is shown that derivatization of the amino group with a phthaloyl moiety increases inhibitory activity of the title compounds, cf. (IIIc) and (IIId). The potent inhibitors (III) and (V) are non-peptidic,
Stereospecific Synthesis and Biological Evaluation of Farnesyl Diphosphate Isomers. -The diphosphates (Ia) and (II) are found to be very potent substrates for mammalian protein-farnesyl transferase. The isomer (Ib) is a submicromolar inhibitor of the transferase. -(SHAO, YING; EUMMER,