Michio Murata, Hideo Naoki, Shigeki Matsunaga, Masayuki Satake, Takeshi Yasumoto. Structure and partial stereochemical assignments for maitotoxin, the most toxic and largest natural non-biopolymer. „J. Am. Chem. Soc.”. 116, s. 7098–7107, 1994. DOI: 10.1021/ja00095a013.
A.R. Gallimore, J.B. Spencer. Stereochemical uniformity in marine polyether ladders--implications for the biosynthesis and structure of maitotoxin. „Angew Chem Int Ed Engl”. 45 (27), s. 4406–4413, 2006. DOI: 10.1002/anie.200504284. PMID: 16767782.
K.C. Nicolaou, M.O. Frederick. On the structure of maitotoxin. „Angew Chem Int Ed Engl”. 46 (28), s. 5278–5282, 2007. DOI: 10.1002/anie.200604656. PMID: 17469088.
F. Gusovsky, J.W. Daly. Maitotoxin: a unique pharmacological tool for research on calcium-dependent mechanisms. „Biochem Pharmacol”. 39 (11), s. 1633–1639, 1990. DOI: 10.1016/0006-2952(90)90105-T. PMID: 1971510.
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A.R. Gallimore, J.B. Spencer. Stereochemical uniformity in marine polyether ladders--implications for the biosynthesis and structure of maitotoxin. „Angew Chem Int Ed Engl”. 45 (27), s. 4406–4413, 2006. DOI: 10.1002/anie.200504284. PMID: 16767782.
K.C. Nicolaou, M.O. Frederick. On the structure of maitotoxin. „Angew Chem Int Ed Engl”. 46 (28), s. 5278–5282, 2007. DOI: 10.1002/anie.200604656. PMID: 17469088.
F. Gusovsky, J.W. Daly. Maitotoxin: a unique pharmacological tool for research on calcium-dependent mechanisms. „Biochem Pharmacol”. 39 (11), s. 1633–1639, 1990. DOI: 10.1016/0006-2952(90)90105-T. PMID: 1971510.