1,2,3,4,6-Penta-<i>O</i>-galloylglucose within Galla Chinensis Inhibits Human LDH-A and Attenuates Cell Proliferation in MDA-MB-231 Breast Cancer Cells

<div>Molecular docking studies (PGG inhibition of human LDH-A). (a) Structure of 1,2,3,4,6-<i>O</i>-galloy1-<i>β</i>-D-glucose, pentagalloylglucose. (b) Binding mode of compound CID65238, PGG, in the coenzyme active site of<i> h</i>LDH-A (PDB: 1∣10). (c) Simplified binding mode of compound CID65238, PGG, in the coenzyme binding site of<i> h</i>LDH-A (PDB: 1∣10).</div>

Evidence-Based Complementary and Alternative Medicine

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Figure 4

Figure 4: 1,2,3,4,6-Penta-<i>O</i>-galloylglucose within Galla Chinensis Inhibits Human LDH-A and Attenuates Cell Proliferation in MDA-MB-231 Breast Cancer Cells 

Figure 4 | 1,2,3,4,6-Penta-O-galloylglucose within Galla Chinensis Inhibits Human LDH-A and Attenuates Cell Proliferation in MDA-MB-231 Breast Cancer Cells 