Exploration on the Interaction Ability of Antitumor Compound Bis-[2,6-difluoro-N-(hydroxyl-<κ>O)benzamidato-<κ>O]dibutylitin(IV) with Human Peroxisome Proliferator-Activated Receptor hPPARγ

<div>The docking results of DBDF2,6T to hPPARγ protein: (a) the generated pocket of hPPARγ protein; (b) hydrogen bond graph of DBDF2,6T to the interacted residues of the hPPARγ protein. The yellow lines in the picture represent the hydrogen bond.</div>

Bioinorganic Chemistry and Applications

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Figure 8

Figure 8: Exploration on the Interaction Ability of Antitumor Compound Bis-[2,6-difluoro-N-(hydroxyl-<κ>O)benzamidato-<κ>O]dibutylitin(IV) with Human Peroxisome Proliferator-Activated Receptor hPPARγ

Figure 8 | Exploration on the Interaction Ability of Antitumor Compound Bis-[2,6-difluoro-N-(hydroxyl-O)benzamidato-O]dibutylitin(IV) with Human Peroxisome Proliferator-Activated Receptor hPPARγ 