A new derivative of ursolic acid containing dual functionality was synthesized. Molecular docking studies and in vitro analysis indicated promising COX inhibition potential for the molecule. The synthesis, characterization, in silico and in vitro studies of the molecule are described here.

中文翻译：

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熊果酸-2-（2-噻吩亚基）-恶二唑杂化分子的半合成及其对COX抑制作用的评价

合成了具有双重功能的熊果酸的新衍生物。分子对接研究和体外分析表明，该分子具有良好的COX抑制潜力。本文描述了该分子的合成，表征，计算机模拟和体外研究。