𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis and rapid purification of 32P-labeled photoactive analogs of farnesyl pyrophosphate

✍ Scribed by Tammy C. Turek; Igor Gaon; Mark D. Distefano


Publisher
John Wiley and Sons
Year
1997
Tongue
French
Weight
406 KB
Volume
39
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Inhibitors of Protein:Farnesyl Transfera
✍ Mark Overhand; Hanneke R. Stuivenberg; Elsbet Pieterman; Louis H. Cohen; Rick E. πŸ“‚ Article πŸ“… 1998 πŸ› Elsevier Science 🌐 English βš– 297 KB

Novel diphosphonate homologs 7a-7c, and their cyclic counterparts 8a-8c, of the previously synthesized farnesyl pyrophosphate analogs 1 and 2 were prepared and tested for their inhibition potency and specificity of the enzymes PFT and PGGT-I. Compound 2 was shown to be the most potent inhibitor of P

Synthesis of high specific activity 35S-
✍ Tamara A. Kale; Conrad Raab; Nathan Yu; Evelyn Aquino; Dennis C. Dean; Mark D. D πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 French βš– 321 KB

## Abstract Prenylated cysteine analogs, which mimic the prenylated cysteine residue of prenylated GTP‐binding proteins (G‐proteins), have been used in a variety of contexts for the study of prenylated G‐protein behavior. In earlier work in this area, we prepared the photoactive analog [^35^S]**4**