Effects of chemical modification of ursodeoxycholic acid on TGR5 activation

Y Iguchi, T Nishimaki-Mogami… - Biological and …, 2011 - jstage.jst.go.jp
Y Iguchi, T Nishimaki-Mogami, M Yamaguchi, F Teraoka, T Kaneko, M Une
Biological and Pharmaceutical Bulletin, 2011jstage.jst.go.jp
MATERIALS AND METHODS General TLC was performed on silica gel precoated TLC
aluminum sheets (0.2 mm thickness, Merck, Germany). NMR spectra were measured at
600MHz on a JEOL ECA-600 spectrometer using chloroform-d5 as a solvent and
tetramethylsilane as internal standard. GC-MS was carried out on GCMS-QP2010
(Shimadzu, Kyoto, Japan) under the following conditions: column, DB-1MS (0.25 mm15. 0
m); column oven temperature, 70—250 C at a rate of 20 C/min with initial time of 1 min …
MATERIALS AND METHODS
General TLC was performed on silica gel precoated TLC aluminum sheets (0.2 mm thickness, Merck, Germany). NMR spectra were measured at 600MHz on a JEOL ECA-600 spectrometer using chloroform-d5 as a solvent and tetramethylsilane as internal standard. GC-MS was carried out on GCMS-QP2010 (Shimadzu, Kyoto, Japan) under the following conditions: column, DB-1MS (0.25 mm15. 0 m); column oven temperature, 70—250 C at a rate of 20 C/min with initial time of 1 min, followed by 250—290 C at a rate of 2 C/min with final time of 2 min; injection port temperature, 300 C; ion source temperature, 200 C; pressure of helium carrier gas, 150 kPa; ionizing voltage, 70 V. Bile acid samples were treated with freshly prepared ethereal diazomethane solution at room temperature for 1 h, and the resulting methyl esters were chromatographed as their trimethylsilyl (TMS) ether derivatives.
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