Trichodermamide A and Aspergillazine A, Two Cytotoxic Modified Dipeptides from a Marine-Derived Fungus Spicaria elegans |
Liu Rui
(Key laboratory of Marine Drugs, Chinese Ministry of Education, Institute of Marine Drugs and Food, Ocean University of China)
Gu Qian-Qun (Key laboratory of Marine Drugs, Chinese Ministry of Education, Institute of Marine Drugs and Food, Ocean University of China) Zhu Wei-Ming (Key laboratory of Marine Drugs, Chinese Ministry of Education, Institute of Marine Drugs and Food, Ocean University of China) Cui Cheng-Bin (Beijing Institute of Pharmacology and Toxicology, AMMS) Fan Guo-Tao (Key laboratory of Marine Drugs, Chinese Ministry of Education, Institute of Marine Drugs and Food, Ocean University of China) |
1 | Caro, E., Starks, C. M., Jensen, P. R., Fenical, W., Lobkovsky, E., and Clardy, J., Trichodermamides A and B, cytotoxic modified dipeptides from the marine-derived fungus trichoderma virens. J. Nat. Prod., 66, 423-426 (2003) DOI ScienceOn |
2 | Cui, C. B., Wang, H., Han, B., Cai, B., Luo, A. Q., Song, Y. X., and Zhou, P. J., Elaiophylins, new cell cycle inhibitors and apoptosis inducers, produced by streptomyces pseudoverticillus II structures and biological properties. Chin. J. Antbiot., 26, 165-170 (2001a) |
3 | Bugni, T. B. and Ireland, C. M., Marine-derived fungi: a chemically and biologically diverse group of microorganisms. Nat. Prod. Rep., 21, 143-163 (2004) DOI ScienceOn |
4 | Lin, Y. C., Shao, Z. Y., Jiang, G., Zhou, S., Cai, J., Vrijmoed, L. L. P., and Jones, E. B. G., Penicillazine, a unique quinolone derivative with 4H-5,6-dihydro-1,2-oxazine ring system from the marine fungus penicillium sp. (strain #386) from the South China Sea. Tetrahedron Lett., 56, 9607-9609 (2000) DOI ScienceOn |
5 | Liu, R., Gu, Q. Q., Zhu, W. M., Cui, C. B., Fang, Y. C., Zhu,T. J., and Liu, H. B., Three new 10-phenyl-[12]cytochalasins , and from marine-derived fungus Spicaria elegans. J. Nat. Prod., (2005, submitted) |
6 | Mosmann, T. J., Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. Immunol. Methods, 65, 55-63 (1983) DOI PUBMED ScienceOn |
7 | Capon, R. J., Ratnayake, R., Stewart, M., Lacey, E., Tennant, S., and Gill, J. H., Aspergillazines A–E: novel heterocyclic dipeptides from an Australian strain of Aspergillus unilateralis. Org. Biomol. Chem., 3, 123-129 (2005) DOI ScienceOn |
8 | Cui, C. B., Wang, H., Han, B., and Song, Y. X., Elaiophylins, new cell cycle inhibitors and apoptosis inducers, produced by streptomyces pseudoverticillus (III) structural and NMR studies. Chin. J. Med. Chem., 39, 25-31 (2001b) |