Isolation of antiplasmodial anthraquinones from Kniphofia ensifolia, and synthesis and structure-activity relationships of related compounds

Bioorg Med Chem. 2014 Jan 1;22(1):269-76. doi: 10.1016/j.bmc.2013.11.032. Epub 2013 Nov 26.

Abstract

Bioassay-guided separation of the South African plant Kniphofia ensifolia for antiplasmodial activity led to the isolation of two new anthraquinones, named kniphofiones A and B (3 and 4), together with three known bioactive anthraquinone monomers (1, 2 and 5), and four known bisanthraquinones (6-9). The structures of the two new compounds were elucidated based on analyses of their 1D and 2D NMR spectra and mass spectrometric data. The dimeric compounds 6 and 7 displayed the strongest antiplasmodial activity among all the isolated compounds, with IC₅₀ values of 0.4 ± 0.1 and 0.2 ± 0.1 μM, respectively. The two new compounds displayed modest activities, with IC₅₀ values of 26 ± 4 and 9 ± 1 μM, respectively. Due to the synthetic accessibility of the new compounds and the increased activity shown by the dimeric compounds, a structure-activity relationship study was conducted. As a result, one analogue of kniphofione B (4), the caffeic acid derivative of aloe-emodin, was found to have the highest activity among all the aloe-emodin derivatives, with an IC50 value of 1.3 ± 0.2 μM.

Keywords: Anthraquinone; Antiplasmodial acitivity; BVTJETXSTYXTDR-VOTSOKGWSA-N; BXWGUDGILDGCGB-UHFFFAOYSA-N; CUKVWNAGSQVAJV-UHFFFAOYSA-N; DBAJNFVKBYXSGU-DUXPYHPUSA-N; DDXMLLFCNJDJDZ-FNORWQNLSA-N; DVLGUQIRWOBEAE-UHFFFAOYSA-N; DZIWALDLFXZKAP-VQHVLOKHSA-N; FSQDQCKBPJZGSC-RMKNXTFCSA-N; FUECAILUKAJTBR-UHFFFAOYSA-N; GJDUVVABRMOOQT-UHFFFAOYSA-N; HLOQRMGUBNDJOS-MDZDMXLPSA-N; HOVDZHKFZHIEPB-UHFFFAOYSA-N; IZDBQZFKJYYUGE-MDZDMXLPSA-N; JNAZKJLAUIOKDJ-UHFFFAOYSA-N; KCZMHHVFUMWLAY-RMKNXTFCSA-N; KSTMMFCURGNHNW-UHFFFAOYSA-N; Kniphofia ensifolia; LQGUBLBATBMXHT-UHFFFAOYSA-N; MSPWCCZZOGHZHE-UHFFFAOYSA-N; NRVKYGSWTHZIQC-UHFFFAOYSA-N; PCJVJTNTIXLPGR-UHFFFAOYSA-N; RJHCHYHEHFGDLC-JXMROGBWSA-N; ROHPHZDISZCEMO-UHFFFAOYSA-N; Structure–activity relationship; UMHLRYWUBPIPAY-JXMROGBWSA-N; WPPHHEBOIPHPLG-VQHVLOKHSA-N; YDQWDHRMZQUTBA-UHFFFAOYSA-N; YRUMLFPFVRGJGH-UHFFFAOYSA-N; YXSQXZFTAVZWMO-BQYQJAHWSA-N; ZRRZSYXEHVZHQQ-UHFFFAOYSA-N.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Antimalarials / chemistry*
  • Antimalarials / pharmacology
  • Cell Proliferation
  • Humans
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Structure-Activity Relationship

Substances

  • Antimalarials