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Search for "baicalein" in Full Text gives 3 result(s) in Beilstein Journal of Organic Chemistry.

Host–guest interaction and properties of cucurbit[8]uril with chloramphenicol

  • Lin Zhang,
  • Jun Zheng,
  • Guangyan Luo,
  • Xiaoyue Li,
  • Yunqian Zhang,
  • Zhu Tao and
  • Qianjun Zhang

Beilstein J. Org. Chem. 2021, 17, 2832–2839, doi:10.3762/bjoc.17.194

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  • cucurbit[n]urils can be used as non-toxic and safe drug carriers [29][30][31], among which cucurbit[8]uril (Q[8]) [32] has a large cavity. Q[8] interacts with a variety of small drug molecules such as chrysin, oroxin A and B, baicalein, etc., which can enhance the solubility, stability, antioxidant and
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Published 03 Dec 2021

Host–guest interaction of cucurbit[8]uril with oroxin A and its effect on the properties of oroxin A

  • Zhishu Zeng,
  • Jun Xie,
  • Guangyan Luo,
  • Zhu Tao and
  • Qianjun Zhang

Beilstein J. Org. Chem. 2020, 16, 2332–2337, doi:10.3762/bjoc.16.194

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  • [21], can help to reduce the side effects and toxicity of the drug [22]. Oroxin A (OA, baicalein-7-O-glucoside, Figure 1A) is one of the active ingredients isolated from the traditional herbal medicine Oroxylum indicum (L.) Kurz of Asian countries [23][24]. Accumulating studies have shown the
  • properties of OA. Our results provide an approach and theoretical basis for the development and utilization of oroxin A. Compared with the literature [31][32], it is found that although baicalein, oroxin B and oroxin A have the same aglycone, but the complex inclusion modes with Q[8] are different, It shows
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Published 22 Sep 2020

The interaction between cucurbit[8]uril and baicalein and the effect on baicalein properties

  • Xiaodong Zhang,
  • Jun Xie,
  • Zhiling Xu,
  • Zhu Tao and
  • Qianjun Zhang

Beilstein J. Org. Chem. 2020, 16, 71–77, doi:10.3762/bjoc.16.9

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  • Xiaodong Zhang Jun Xie Zhiling Xu Zhu Tao Qianjun Zhang Key Laboratory of Macrocyclic and Supramolecular Chemistry of Guizhou Province, Guizhou University, Guiyang 550025, China 10.3762/bjoc.16.9 Abstract The host–guest interactions between baicalein (BALE) and cucurbit[8]uril (Q[8]) and the
  • corresponding properties of the inclusion complex were studied using 1H NMR, IR and UV–vis spectroscopy and DTA. The results showed that BALE forms an inclusion compound (1:1) with Q[8], and the properties of baicalein are changed by cucurbit[8]uril. Keywords: baicalein; cucurbit[8]uril; host–guest interaction
  • ; inclusion complex; properties; Introduction Baicalein (5,6,7-trihydroxyflavonoid) has a molecular formula of C15H10O5 (BALE, Figure 1) and is a natural flavonoid found in the roots of Scutellaria baicalensis Georgi [1]. The compound displays pharmacological activity such as antimicrobial, anti-inflammatory
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Published 10 Jan 2020
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