ORIGINAL ARTICLEPharmacognosy MagazineVol. 13 | Issue 50s | 2017 | pp. S289–93Open access
Antiproliferative Activity of Haematoxylum brasiletto H. Karst
- 1,
- 2,
- 3,
- 4,
- 5,
- 5,
- 5,
- 5*
- 1 Laboratory of Chemistry of Natural Products, School of Chemical and Biological Sciences, Guerrero State University, Chilpancingo, Guerrero, Mexico.
- 2 Department of Natural Products, Institute of Chemistry, Mexico National Autonomous University (UNAM), Ciudad de México, Mexico.
- 3 School of Regional Development Sciences, Guerrero State University, Acapulco, Guerrero, Mexico.
- 4 Department of Chemical and Biological Sciences, Sonora State University, Blvd. Luis Donaldo Colosio esq. Rosales s/n Col. Centro, Hermosillo, Sonora, Mexico.
- 5 National Institute of Cancerology, Tlalpan, Ciudad de México, Mexico.
Published in Pharmacognosy Magazine
Correspondence: RE RE
National Institute of Cancerology, Tlalpan, Ciudad de México, Mexico.
Email: rrobles@guayacan.uson.mx
Copyright: © 2017 Manuscript Technomedia. This is an open access article.
- Published:
- Jul 11, 2017
- Received:
- Oct 19, 2016
- Accepted:
- Nov 17, 2016
- DOI:
- 10.4103/pm.pm_466_16
How to cite
J, J., M, M., JL, J., LP, L., M, M., C, C., E, E., & RE, R. (2017). Antiproliferative Activity of Haematoxylum brasiletto H. Karst. Pharmacognosy Magazine, 13(50s), S289–93. https://doi.org/10.4103/pm.pm_466_16
Abstract
Background: Haematoxylum brasiletto is a tree that grows in Central America, commonly known as “Palo de Brasil,” which is used in the traditional medicine for the treatment of cancer and gastric ulcers. Objective: The aim of this study was to isolate the compounds responsible for antiproliferative activity of H. brasiletto. Materials and Methods: A bioassay‑guided fractionation of ethanol extract of H. brasiletto was performed using 3‑(4, 5‑dimethylthiazol‑2‑yl)‑2, 5‑diphenyltetrazolium bromide cell proliferation assay to measure the antiproliferative activity on six human cancer cell lines (A549, LS180, HeLa, SiHa, MDA‑MB‑231, and NCI‑H1299) and one human noncancer cell line (ARPE‑19). The ethanol extract was partitioned with hexane, dichloromethane, and ethyl acetate. The active dichloromethane fraction was fractioned by silica‑column chromatography, and active subfractions were separated using preparative‑thin layer chromatography. The chemical structure of an isolated compound was elucidated with different chemical and spectroscopic methods. Results: The flavonoid brazilin (1) was isolated from the heartwood of H. brasiletto. The measurement of antiproliferative activity showed that brazilin can inhibit the growth of SiHa, MDA‑MB‑231, A549, and NCI‑H1299 cell lines by 50% at doses of 44.3, 48.7, 45.4, and 48.7 µM, respectively. Furthermore, the flavonoid showed a high antiproliferative activity on LS 180 and HeLa with IC50 values of 62.2 and 71.9 µM, respectively. Brazilin also exhibited a high antiproliferative activity on the human noncancer cell line ARPE‑19 with an IC50 value of 37.9 µM. Conclusions: Brazilin: (6aS,11bR)‑7,11b‑Dihidro‑6H‑indeno[2, 1‑c] cromeno‑3,6a, 9,10‑tetrol was isolated; this compound demonstrated antiproliferative activity against several human cancer cell lines. This work demonstrated that brazilin, a flavonoid isolated and characterized of H. brasiletto, has antiproliferative activity against cancer cell lines. Brazilin is able to inhibit the growth of SiHa, MDA-MB-231, A549 and NCI-H1299 cancerous cell lines Brazilin exhibited a moderate antiproliferative activity on the human non-cancer cell line ARPE-19 Brazilin demonstrated to have antiproliferative activity against human cancer cell lines and could be a potential source of anticancer agents.
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Article metadata
| Title | Antiproliferative Activity of Haematoxylum brasiletto H. Karst |
|---|---|
| Authors | J J; M M; JL JL; LP LP; M M; C C; E E; RE RE |
| Affiliations | Laboratory of Chemistry of Natural Products, School of Chemical and Biological Sciences, Guerrero State University, Chilpancingo, Guerrero, Mexico.; Department of Natural Products, Institute of Chemistry, Mexico National Autonomous University (UNAM), Ciudad de México, Mexico.; School of Regional Development Sciences, Guerrero State University, Acapulco, Guerrero, Mexico.; Department of Chemical and Biological Sciences, Sonora State University, Blvd. Luis Donaldo Colosio esq. Rosales s/n Col. Centro, Hermosillo, Sonora, Mexico.; National Institute of Cancerology, Tlalpan, Ciudad de México, Mexico. |
| Corresponding author | rrobles@guayacan.uson.mx |
| Journal | Pharmacognosy Magazine |
| Volume / Issue | Vol. 13, Issue 50s (2017) |
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