Product Information
- 2,6,9,11-Tridecatetraen-4-ol, 13-(4-hydroxy-5,6-dimethoxy-3-methyl-2-pyridyl)-3,5,7,11-tetramethyl-, (all-E)-(4R,5R)-
- 2-[(2E,5E,7E,9R,10R,11E)-10-Hydroxy-3,7,9,11-tetramethyl-2,5,7,11-tridecatetraen-1-yl]-5,6-dimethoxy-3-methyl-4-pyridinol
- 2-[(2E,5E,7E,9R,10R,11E)-10-hydroxy-3,7,9,11-tetramethyltrideca-2,5,7,11-tetraen-1-yl]-5,6-dimethoxy-3-methylpyridin-4-ol
- 4-Pyridinol, 2-(10-hydroxy-3,7,9,11-tetramethyl-2,5,7,11-tridecatetraenyl)-5,6-dimethoxy-3-methyl-, [R-[R*,R*-(all-E)]]-
- 4-Pyridinol, 2-[(2E,5E,7E,9R,10R,11E)-10-hydroxy-3,7,9,11-tetramethyl-2,5,7,11-tridecatetraenyl]-5,6-dimethoxy-3-methyl-
- 4-pyridinol, 2-[(2E,5E,7E,9R,10R,11E)-10-hydroxy-3,7,9,11-tetramethyl-2,5,7,11-tridecatetraen-1-yl]-5,6-dimethoxy-3-methyl-
- Ar 054
- Piericidin A<sub>1</sub>
- Piericidine A
- Shaoguanmycin B
- See more synonyms
- Sn 198E
Piericidin A is a polymeric compound that inhibits the synthesis of RNA and DNA by binding to the enzyme polymerase chain. It has been shown to be effective in inhibiting the growth of photosynthetic bacteria, with a rate constant of 0.8 x 10^-5 L mol^-1 s. Piericidin A has also been shown to have anti-axonal effects on neurons, as well as inhibit tubulointerstitial injury due to acute toxicities and inhibitor molecules. The biochemical properties of this compound have been studied using preparative high-performance liquid chromatography (HPLC) and enzymatic assays. Experiments with an experimental model have shown that piericidin A has a high affinity for hydrogen bonding interactions, which makes it an active inhibitor.
Chemical properties
Technical inquiry about: 3D-FP172915 Piericidin A
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