Antiproliferative Effect and the Isolated Compounds of Pouzolzia indica
Previous report showed the high potent antiproliferative effect of the methanolic part extracted from the aerial parts of Pouzolzia indica on NB4 and HT93A acute leukemic cell lines with the IC50 values of 28.5 and 49.8 μg/mL, respectively. The bioassay-guided fractionation of the methanolic part ga...
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doaj-8506dc38648b4133b1fc93b0e78aa4ad2020-11-24T22:28:06ZengHindawi LimitedEvidence-Based Complementary and Alternative Medicine1741-427X1741-42882013-01-01201310.1155/2013/342352342352Antiproliferative Effect and the Isolated Compounds of Pouzolzia indicaChanyapat Sangsuwon0Weena Jiratchariyakul1Yaowalak U-pratya2Tanawan Kummalue3Department of Pharmacognosy, Faculty of Pharmacy, Mahidol University, Bangkok 10400, ThailandDepartment of Pharmacognosy, Faculty of Pharmacy, Mahidol University, Bangkok 10400, ThailandDepartment of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, ThailandDepartment of Clinical Pathology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, ThailandPrevious report showed the high potent antiproliferative effect of the methanolic part extracted from the aerial parts of Pouzolzia indica on NB4 and HT93A acute leukemic cell lines with the IC50 values of 28.5 and 49.8 μg/mL, respectively. The bioassay-guided fractionation of the methanolic part gave 5 fractions, that is, FFI–FFV. FFII, FFIII, and FFIV inhibited the above leukemic cell lines with the IC50 values of 15.1 (FFII), 14.4 (FFIII), 32.1 (FFIV), and 31.0 (FFII), 9.7 (FFIII), 10.5 (FFIV) μg/mL, respectively. The compounds in these fractions were isolated using chromatographic technique. FFII contained friedelin 1, 28-hydroxy-3-friedelanone 2, and 7-methoxy-coumarin 3. FFIII contained 6, 7-dimethoxy-coumarin 4, scopoletin 5, methyl caffeate 6. FFIV contained sitosteryl glucoside 7 and a supposed glycosphingolipid 8. The chemical structures were elucidated by spectroscopic methods.http://dx.doi.org/10.1155/2013/342352 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chanyapat Sangsuwon Weena Jiratchariyakul Yaowalak U-pratya Tanawan Kummalue |
spellingShingle |
Chanyapat Sangsuwon Weena Jiratchariyakul Yaowalak U-pratya Tanawan Kummalue Antiproliferative Effect and the Isolated Compounds of Pouzolzia indica Evidence-Based Complementary and Alternative Medicine |
author_facet |
Chanyapat Sangsuwon Weena Jiratchariyakul Yaowalak U-pratya Tanawan Kummalue |
author_sort |
Chanyapat Sangsuwon |
title |
Antiproliferative Effect and the Isolated Compounds of Pouzolzia indica |
title_short |
Antiproliferative Effect and the Isolated Compounds of Pouzolzia indica |
title_full |
Antiproliferative Effect and the Isolated Compounds of Pouzolzia indica |
title_fullStr |
Antiproliferative Effect and the Isolated Compounds of Pouzolzia indica |
title_full_unstemmed |
Antiproliferative Effect and the Isolated Compounds of Pouzolzia indica |
title_sort |
antiproliferative effect and the isolated compounds of pouzolzia indica |
publisher |
Hindawi Limited |
series |
Evidence-Based Complementary and Alternative Medicine |
issn |
1741-427X 1741-4288 |
publishDate |
2013-01-01 |
description |
Previous report showed the high potent antiproliferative effect of the methanolic part extracted from the aerial parts of Pouzolzia indica on NB4 and HT93A acute leukemic cell lines with the IC50 values of 28.5 and 49.8 μg/mL, respectively. The bioassay-guided fractionation of the methanolic part gave 5 fractions, that is, FFI–FFV. FFII, FFIII, and FFIV inhibited the above leukemic cell lines with the IC50 values of 15.1 (FFII), 14.4 (FFIII), 32.1 (FFIV), and 31.0 (FFII), 9.7 (FFIII), 10.5 (FFIV) μg/mL, respectively. The compounds in these fractions were isolated using chromatographic technique. FFII contained friedelin 1, 28-hydroxy-3-friedelanone 2, and 7-methoxy-coumarin 3. FFIII contained 6, 7-dimethoxy-coumarin 4, scopoletin 5, methyl caffeate 6. FFIV contained sitosteryl glucoside 7 and a supposed glycosphingolipid 8. The chemical structures were elucidated by spectroscopic methods. |
url |
http://dx.doi.org/10.1155/2013/342352 |
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