- Palytoxin
Drugbox
IUPAC_name = unable to be assigned
width=300
CAS_number=77734-91-9
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DrugBank=
C=129 | H=223 | N=3 | O=54
molecular_weight = 2680.13 g.mol-1
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routes_of_administration=Palytoxin is an incredibly complex marine natural product containing 71 asymmetric centers. Palytoxin, isolated from soft coral, is considered to be one of the most toxic non-peptide substances known, second only to
maitotoxin . Palytoxin was originally isolated in1971 inHawaii from the seaweed-like coral, "Limu make o hana (Seaweed of Death from Hana)" [Clayden, J., Greeves, N. (2000), pages 19-21] . Later, in 1982 its full chemical structure was published by Prof. Daisuke Uemura and coworkers at Nagoya University [Chemical Society of Japan, et al. (2005). "CSJ Award-2005 Prof. Daisuke Uemura" Retrieved on 24 July, 2007 from [http://www.chemistry.or.jp/csj-en/membership/awards/achieve/2005-uemura.html http://www.chemistry.or.jp/csj-en/membership/awards/achieve/2005-uemura.html] Chemical Soc. of Japan, Prof. D. Uemura] [Chemical Society of Japan, et al. (2005), -- "Its structural determination presented many difficulties. Dr. Uemura elucidated its planar structure in 1981 by repeatedly carrying out site-specific oxidative degradation and determined the structure of the degraded products using a sample that was originally isolated from Palythoa tuberculosa of Okinawa [n] origin."] [Stereochemistry of Palytoxin. 4. Complete Structure, J. K. Cha, W. J. Christ, J. M. Finan, H. Fujioka, Y. Kishi, L. L. Klein, S. S. Ko, J. Leder, W. W. McWhorter, Jr., K. -P. Pfaff, M. Yonaga, D. Uemura, and Y. Hirata, J. Am. Chem. Soc., 104, 7369-7371 (1982)] . Professor Yoshito Kishi's group atHarvard University first synthesized palytoxin in1994 ["Total Synthesis of Palytoxin Carboxylic Acid and Palytoxin Amide," R.W. Armstrong, J.-M. Beau, S.H. Cheon, W.J. Christ, H. Fujioka, W.-H. Ham, L.D. Hawkins, H. Jin, S.H. Kang, Y. Kishi, M.J. Martinelli, W.W. McWhorter, Jr., M. Mizuno, M. Nakata, A.E. Stutz, F.X. Talamas, M. Taniguchi, J.A. Tino, K. Ueda, J. Uenishi, J.B. White, and M. Yonaga, J. Am. Chem. Soc., 111, 7530 (1989)] ["Synthesis of Palytoxin from Palytoxin Carboxylic Acid", E.M. Suh and Y. Kishi, J. Am. Chem. Soc., 116, 11205 (1994).] . This feat is still considered today by many to be the greatest synthetic accomplishment ever, due to its complexity in structure.Palytoxin targets the sodium-potassium pump
protein by binding to the molecule such that the molecule is locked in a position where it allowspassive transport of both thesodium andpotassium ions, thereby destroying the ion gradient that is essential for most cells.Typical symptoms of palytoxin poisoning are angina-like chest pains,
asthma -like breathing difficulties,tachycardia , unstableblood pressure ,hemolysis (destruction of red blood cells), and anelectrocardiogram showing an exaggerated T wave. The onset of symptoms is rapid, and death usually follows just minutes after.Animal studies have shown that
vasodilator s, such as papverine and isosorbide nitrate, can be used asantidotes . The animal experiments only showed benefit if the antidotes were injected into theheart immediately following exposure. [cite journal | author = Wiles J, Vick J, Christensen M | title = Toxicological evaluation of palytoxin in several animal species | journal = Toxicon | volume = 12 | issue = 4 | pages = 427–33 | year = 1974 | pmid = 4155146 | doi = 10.1016/0041-0101(74)90011-7] Treatment in humans is symptomatic and supportive.Footnotes
References
*Nelson, David L. and Cox, Michael M.. "Lehninger Principles of Biochemistry, 4th Edition". Published by Freeman in 2005. p.399 mentions palytoxin.
*Clayden, R., Greeves, N. (2000) "Organic chemistry" Oxford publishing
* [http://www.pnas.org/content/vol100/issue2/images/medium/pq0437775001.gifStructure of palytoxin] (molecule labelled "B")
* [http://www.cbwinfo.com/Biological/Toxins/Palytoxin.html CBWInfo]
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