Naraganahalli R Thimmegowda, Chanmi Park, Bettaswamigowda Shwetha, Krisada Sakchaisri, Kangdong Liu, Joonsung Hwang, Sangku Lee, Sook J Jeong, Nak K Soung, Jae H Jang, In-Ja Ryoo, Jong S Ahn, Raymond L Erikson, Bo Y Kim
Index: Chem. Biol. Drug Des. 85(5) , 638-44, (2015)
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In this study, we have synthesized novel water soluble derivatives of natural compound aloe emodin 4(a-j) by coupling with various amino acid esters and substituted aromatic amines, in an attempt to improve the anticancer activity and to explore the structure-activity relationships. The structures of the compounds were determined by (1) H NMR and mass spectroscopy. Cell growth inhibition assays revealed that the aloe emodin derivatives 4d, 4f, and 4i effectively decreased the growth of HepG2 (human liver cancer cells) and NCI-H460 (human lung cancer cells) and some of the derivatives exhibited comparable antitumor activity against HeLa (Human epithelial carcinoma cells) and PC3 (prostate cancer cells) cell lines compared to that of the parent aloe emodin at low micromolar concentrations. © 2014 John Wiley & Sons A/S.
Structure | Name/CAS No. | Molecular Formula | Articles |
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Aloeemodin
CAS:481-72-1 |
C15H10O5 |
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High-affinity, non-nucleotide-derived competitive antagonist...
2009-06-25 [J. Med. Chem. 52 , 3784-93, (2009)] |
Expression profile of genes modulated by Aloe emodin in huma...
2014-01-01 [Asian Pac. J. Cancer Prev. 15(11) , 4499-505, (2014)] |
Hypericins and thioredoxin reductase: Biochemical and dockin...
2011-01-01 [Bioorg. Med. Chem. 19 , 631-41, (2011)] |
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