Isopentenyl thiolodiphosphate (ISPP) is an analog of IPP in which the non-bridging oxygen has been replaced by sulfur resulting in a less-reactive compound.
Provided as the tris-ammonium salt
Featured In Publications
1. Phan, R. M. and C. D. Poulter (2001). “Synthesis of (S)-Isoprenoid Thiodiphosphates as Substrates and Inhibitors.” The Journal of Organic Chemistry 66(20): 6705.2. Lee, L. V., B. Granda, et al. (2010). “Biophysical Investigation of the Mode of Inhibition of Tetramic Acids, the Allosteric Inhibitors of Undecaprenyl Pyrophosphate Synthase.” Biochemistry 49(25): 5366.3. Sandoval, C., M. Ayson, et al. (2014) “Use of pantothenate as a metabolic switch increases the genetic stability of farnesene producing Saccharomyces cerevisiae” Metabolic Engineering 25, 215-226.4. Chan, YT, TP Ko, et al. (2017) “Crystal Structure and Potential Head-to-Middle Condensation Function of a Z,Z-Farnesyl Diphosphate Synthase” ACS Omega, 2(3), 930-936.
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| Categories | Biochemical Reagents |
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| Filter | Isoprenoid, Isoprenoid Diphosphate |
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| CAS Number | 688307-87-1 |
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| Molecular Formula | C5H21N3O6P2S |
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| Molecular Weight (g/mol) | 313.25 |
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| Purity | >95% |
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| Storage | -20 °C or below |
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