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5 results for “Ilex cornuta”
Fig. 2 in Anti-adipogenic 18,19-seco-ursane stereoisomers and oleane-type saponins from Ilex cornuta leaves
Fig. 2. HPLC separation of compounds 1–3 and 6 (A, a mixture of 1–3 and 6; B, compound 1; C, compound 6; D, compound 2; and E, compound 3). HPLC conditions: an Agilent 1100 series system with a Capcell Pak MGII C18 column (4.6 mm × 250 mm, 5 μm); column temperature, 25 °C, the mobile phase: MeCN-H2O (33:67); flow rate: 1.0 mL/min; detection wavelength, 210 nm.
Fig. 5 in Anti-adipogenic 18,19-seco-ursane stereoisomers and oleane-type saponins from Ilex cornuta leaves
Fig. 5. The inhibitory effect of compounds 1–16 on the PPARγ expression in transfected 3T3-L1-Lenti- PPARγ-Luc cells (n = 4, *: comparison of PPARγ expression with the vehicle control group, #: comparison of PPARγ expression with the positive control, ** P ≤ 0.01, *** P ≤ 0.001). Con and PC represented the vehicle control group (cells treated with 0.1% DMSO) and the positive control (T0070907) at 5 μM, respectively. 1–16 represented compounds 1–16 at 5 μM. Vertical bars represented the standard error of means (SEM).
Fig. 1 in Anti-adipogenic 18,19-seco-ursane stereoisomers and oleane-type saponins from Ilex cornuta leaves
Fig. 1. Chemical structures of compounds 1–16.
Fig. 3 in Anti-adipogenic 18,19-seco-ursane stereoisomers and oleane-type saponins from Ilex cornuta leaves
Fig. 3. Key HMBC correlations of 1–6.
Fig. 4 in Anti-adipogenic 18,19-seco-ursane stereoisomers and oleane-type saponins from Ilex cornuta leaves
Fig. 4. ORTEP drawing of compounds 1, 2, 4, and 6 (A different numbering system might be used for the structure in the text).
ScienceDex guides
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