40617-59-2Relevant academic research and scientific papers
Semi-synthetic analogs of pinitol as potential inhibitors of TNF-α cytokine expression in human neutrophils
Bhat, Khurshid A.,Shah, Bhahwal A.,Gupta, Kuldeep K.,Pandey, Anjali,Bani, Sarang,Taneja, Subhash C.
scheme or table, p. 1939 - 1943 (2009/12/03)
Semi-synthetic analogs of pinitol were subjected to screening by determining TNF-α expression in human neutrophils using flowcytometry. Among the tested compounds, three derivatives displayed more than 50% inhibition of TNF-α cytokine secretion in LPS ind
Enzyme-catalysed synthesis of galactosylated 1D- and 1L-chiro-inositol, 1D-pinitol, myo-inositol and selected derivatives using the β-galactosidase from the thermophile Thermoanaerobacter sp. strain TP6-B1
Hart, Joanne B.,Kroeger, Lars,Falshaw, Andrew,Falshaw, Ruth,Farkas, Erzsebet,Thiem, Joachim,Win, Anna L.
, p. 1857 - 1871 (2007/10/03)
The products from the enzymatic β-D-galactopyranosylation of 1D-chiro-inositol, 1D-pinitol, 1D-3-O-allyl-4-O-methyl-chiro-inositol, 1D-3,4-di-O-methyl-chiro-inositol, 1L-chiro-inositol and myo-inositol in combined yields ranging from 46% to 64% have been
Efficient synthetic routes to fluorinated isosteres of inositol and their effects on cellular growth
Kozikowski, Alan P.,Fauq, Abdul H.,Powis, Garth,Melder, Deborah C.
, p. 4528 - 4531 (2007/10/02)
Efficient synthetic routes to several fluorinated isosteres of inositol have been developed that are based upon the unexpected selectivity observed in the (diethylamido)sulfur trifluoride reaction of polyhydroxylated cyclohexane derivatives. The conversio
