Abstract |
Nodulisporacid A (1) was isolated from a marine-derived fungus Nodulisporium sp. CRIF1, while vermelhotin (5) was obtained from an unidentified fungus CRI247-01 (a member of the Order Pleosporales). Both 1 and 5 occurred as equilibrium E/Z mixtures. Ester derivatives (2 and 3) and vermelhotin (5) showed cytotoxic activity against eleven cancer cell lines. Nodulisporacid A (1) and vermelhotin (5) exhibited moderate antiplasmodial activity.
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Authors | Chairut Kasettrathat, Nattaya Ngamrojanavanich, Suthep Wiyakrutta, Chulabhorn Mahidol, Somsak Ruchirawat, Prasat Kittakoop |
Journal | Phytochemistry
(Phytochemistry)
Vol. 69
Issue 14
Pg. 2621-6
(Oct 2008)
ISSN: 0031-9422 [Print] England |
PMID | 18804825
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antimalarials
- Antineoplastic Agents, Phytogenic
- Biological Products
- Furans
- Pyrrolidines
- Pyrrolidinones
- nodulisporacid A
- vermelhotin
- tetramic acid
- tetronic acid
- 4-Butyrolactone
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Topics |
- 4-Butyrolactone
(analogs & derivatives, isolation & purification, pharmacology)
- Animals
- Antimalarials
(isolation & purification, pharmacology)
- Antineoplastic Agents, Phytogenic
(isolation & purification, pharmacology)
- Biological Products
(isolation & purification, pharmacology)
- Cell Line, Tumor
- Drug Screening Assays, Antitumor
- Furans
(isolation & purification, pharmacology)
- Humans
- Molecular Structure
- Plasmodium falciparum
(drug effects)
- Pyrrolidines
(isolation & purification, pharmacology)
- Pyrrolidinones
(isolation & purification, pharmacology)
- Xylariales
(chemistry)
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