Isopentenyl Diphosphate (IPP)
![]() ![]() |
Catalog No.: I-0050 MW: 297.18 CAS: 116057-53-5 Description: Isoprenoid compounds are a diverse group of natural products which are essential components in all cells. Isoprenoids are biosynthesized from the simple precursors isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Eukaryotes, fungi, and some gram-positive bacteria produce IPP through the mevalonate (MVA) pathway whereas gram-negative and some gram-positive bacteria utilize the non-mevalonate or 2-C-methyl-D-erythritol-4-phosphate (MEP) pathway. |
|||||||
Provided as the tris-ammonium salt Storage-20 °C or belowFeatured in Publications:1) Wouters, J., Y. Oudjama, et al. (2003). "Structure and mechanism of action of isopentenylpyrophosphate- dimethylallylpyrophosphate isomerase." J Am Chem Soc 125(11): 3198-9.2) Schilmiller, A. L., I. Schauvinhold, et al. (2009). "Monoterpenes in the glandular trichomes of tomato are synthesized from a neryl diphosphate precursor rather than geranyl diphosphate." Proceedings of the National Academy of Sciences 106(26): 10865-10870. 3) Bang, S., S. Yoo, et al. (2010). "Farnesyl pyrophosphate is a novel pain-producing molecule via specific activation of TRPV3." J Biol Chem 285(25): 19362-71. Product Keywords: Isopentenyl pyrophosphate, IPP Bulk discounts available, please email echelon@echelon-inc.com for information. |
||||||||
|
||||||||
Additional Information:
Tech Data Sheet - I-0050 |
||||||||
|