4.7 Article

Phthalide-derived oxaspiroangelioic acids A-C with an unprecedented carbon skeleton from an aqueous extract of the Angelica sinensis root head

期刊

CHINESE CHEMICAL LETTERS
卷 32, 期 10, 页码 3257-3260

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.cclet.2021.03.004

关键词

Umbelliferae; Angelica sinensis; Phthalide-derived analogues; Oxaspiroangelioic acidsA-C

资金

  1. National Natural Sciences Founda-tion of China [81630094]
  2. CAMS Innovation Fund for Medical Science (China) [2017-I2M-3-010]
  3. Drug Innovation Major Project (China) [2018ZX09711001-004, 2018ZX09711001-001]

向作者/读者索取更多资源

Three phthalide-derived analogues, oxaspiroangelioic acids A-C, were isolated from aqueous extract of Angelica sinensis root heads. Oxaspiroangelioic acids A and B were separated into enantiomers by chiral HPLC. They share similar inhibiting activity and may be biosynthesized through novel pathways.
Three phthalide-derived analogues, oxaspiroangelioic acids A-C (1-3), were isolated as minor components of an aqueous extract of the Angelica sinensis root heads (guitou). Oxaspiroangelioic acids A and B were racemates separated into enantiomers by chiral HPLC. Their structures including absolute configurations were determined by spectroscopic data analysis, single crystal X-ray diffraction, exciton chirality method and electronic circular dichroism (ECD) calculation. These compounds share an undescribed carbon skeleton, for which biosynthetic pathways are proposed. Compound 1 and its enantiomers showed almost identical activity inhibiting Tandem of P domains in a weak inwardly rectifying K+ channel 1 (TREK-1). (C) 2021 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.

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