Fitoterapia2022,Vol.1597.DOI:10.1016/j.fitote.2022.105194

New cyclopeptide alkaloid of Condalia buxifolia and the absolute stereochemistry of Condaline A

Gehm, Adriana Z. Cunha, Sabrina B. Silva, Bruce W. da Mostardeiro, Marco A. Bastos, Nelci. R. Burrow, Robert A. Caro, Miguel S. B. Dalcol, Ionara I. Morel, Ademir F.
Fitoterapia2022,Vol.1597.DOI:10.1016/j.fitote.2022.105194

New cyclopeptide alkaloid of Condalia buxifolia and the absolute stereochemistry of Condaline A

Gehm, Adriana Z. 1Cunha, Sabrina B. 1Silva, Bruce W. da 1Mostardeiro, Marco A. 1Bastos, Nelci. R. 1Burrow, Robert A. 1Caro, Miguel S. B. 2Dalcol, Ionara I. 1Morel, Ademir F.1
扫码查看

作者信息

  • 1. Univ Fed Santa Maria
  • 2. Univ Fed Santa Catarina
  • 折叠

Abstract

During the course of a study of Condalia buxifolia (Rhamnaceae), one new cyclopeptide alkaloid condaline B (1), together with six known cyclopeptide alkaloids, condaline A (2), and the scutianines B (3), - D (4) and -E (5), frangulanine (6), and 3,4,28-tris-epi-scutianene N (7), were isolated from the rind bark of Condalia buxifolia. Their structures have been confirmed through spectroscopic analyses such as 1D and 2D NMR experiments. The absolute stereochemistry of condaline A (2), was elucidated by X-ray crystal structure determination of its HI salt. In addition, condaline B (1) was obtained synthetically through a structural transformation of condaline A. Meanwhile, the crude methanol extract, the basic ether fraction, and alkaloids 1-7 were tested against various strains of Gram-positive and Gram-negative bacteria and fungus, showing promising antimicrobial activity

Key words

Rhamnaceae/Cyclopeptide alkaloids/Absolute stereochemistry/Condaline B/Antimicrobial activity/Condalia buxifolia/X-RAY CRYSTALLOGRAPHY/PEPTIDE ALKALOIDS/BARK/RHAMNACEAE

引用本文复制引用

出版年

2022
Fitoterapia

Fitoterapia

SCI
ISSN:0367-326X
参考文献量22
段落导航相关论文