1. The efficient synthesis and biological evaluation of justicidin B
- Author
-
Jungyeob Ham, Kyu-Hyuk Jeong, Ha-Neul Ju, Pilju Choi, Hyukjoon Kwon, Young-Tae Park, Taejung Kim, Ji-Yool Kim, Young-Joo Kim, and Cheol Hee Yoon
- Subjects
chemistry.chemical_classification ,Annulation ,Lipopolysaccharide ,Stereochemistry ,Organic Chemistry ,Total synthesis ,Dioxolanes ,Plant Science ,Biochemistry ,Lignans ,Analytical Chemistry ,Phthalide ,Nitric oxide ,Cell Line ,chemistry.chemical_compound ,Mice ,Lactones ,chemistry ,Cell culture ,Animals ,Humans ,Cytotoxicity ,Lactone - Abstract
A facile new synthetic method for the preparation of a Type-A 1-arylnaphthalene lactone skeleton was developed and used to synthesise justicidin B and several derivatives. Key synthesis steps included Hauser-Kraus annulation of a phthalide intermediate and Suzuki-Miyaura cross coupling between a triflated naphthalene lactone intermediate and various potassium organotrifluoroborates. With two exceptions, the derivatives showed significant inhibitory effect on lipopolysaccharide (LPS)-induced nitric oxide (NO) production in mouse macrophages. Moreover, several compounds, including justicidin B, had marked cytotoxicity towards six human tumour cell lines.
- Published
- 2021