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The field of marine medicine has clearly advanced from its early stages of chemical exploration to a new era in which marine-derived drugs are here. Over the next decade,we will see sig nificant numbers of marine drugs being used in the treatment of cancer,other for intense pain and infectious diseases. There will be an expansion of these stud- ies to focus on many therapeutic areas of growing human need.After all,if we are to return to natural products as a source Figure 10.A clo for new drugs,where else might we go? up underwat r photo of the Indonesian sponge Acanthostrongylophora sp.This sponge tains complex molecules of the manzamine cass (manzamine A shown)The manzamines.which ACKNOWLEDGEMENTS I apologize to the many contributors to this field whose workI simply did not have space to describe.I am particularly grateful for the photos provided by sev- 122:12903-12.90 of the national eral colleagues (sce the figures for phote I.Handels .BMy of se c ce 83: .W.LeChemi- credit),which allowed me to adequately Zeiku illustrate their excellent work. Lc31.981-1.984 sts Discri r natu REFERENCES Andersen,RL,and M.Roberge.2005.HTI-286,A Rao.K.V.N. nah s Wah ,DG.L Kingsto nd D.I.N n,eds. R.F.Schinazi,and M.T.Hamann.2004.Three ney CRC Pr nd Fr Boca Raton,FL sponge and their activity against inf ph9 PA 31 5.Einaig stry (I Hay, oy:Whats e Dat 006. pare Copp,M.H.G.Munr North y200(1-2:103-134 kton.C 。 gy.Journal of Che mical Ecology 28(10):1.897 mth 06nmcd php llast accessed Blunt,LW.B.R.Copp.M.H.G.Munro,PT.Northc PR TI Minc and W Eenical cete di 7 Kna P,M.V Risk 5 M Ra Golik.I.C.Ia nd K 1981.1 CPfannkoch,YH.Rogers,and H.O.Smit 1.200 n sequencing of th 415080E 30466-74 1036773-6.776 Look 5.A.,W.Fenical,R.S.Ja and I.Clardy 1986 ONA.bmalgytheAm rican Chemical Society Occanography I Vol 19.No.2.June 2006 119Oceanography Vol. 19, No. 2, June 2006 119 The fi eld of marine medicine has clearly advanced from its early stages of chemical exploration to a new era in which marine-derived drugs are here. Over the next decade, we will see sig￾nifi cant numbers of marine drugs being used in the treatment of cancer, others for intense pain and infectious diseases. There will be an expansion of these stud￾ies to focus on many therapeutic areas of growing human need. After all, if we are to return to natural products as a source for new drugs, where else might we go? ACKNOWLEDGEMENTS I apologize to the many contributors to this fi eld whose work I simply did not have space to describe. I am particularly grateful for the photos provided by sev￾eral colleagues (see the fi gures for photo credit), which allowed me to adequately illustrate their excellent work. REFERENCES Andersen, R.J., and M. Roberge. 2005. HTI-286, A synthetic analog of the antimitotic natural prod￾uct hemiasterlin. Pp. 267–280 in Anticancer Agents from Natural Products, G.M. Cragg, D.G.I. Kings￾ton, and D.J. Newman, eds. CRC Press (Taylor & Francis Group), Philadelphia, PA. Bérdy, J. 2005. Bioactive microbial metabolites. A per￾sonal view. Journal of Antibiotics 58:1–27. Bergmann, W., and R.J. Feeney. 1951. Contributions to the study of marine products XXXII. The nucleo￾sides from sponges. Journal of Organic Chemistry 16:981–987. Blunt, J.W., B.R. Copp, M.H.G. Munro, P.T. Northcote, and M.R. Prinsep. 2003. Marine natural products. Natural Product Reports 20:1–48; doi: 10.1039/ b207130b. Blunt, J.W., B.R. Copp, M.H.G. Munro, P.T. Northcote, and M.R. Prinsep. 2004. Marine natural products. Natural Product Reports 21:1-49; doi: 10.1039/ b305250h. Blunt, J.W., B.R. Copp, M.H.G. Munro, P.T. Northcote, and M.R. Prinsep. 2005. Marine natural products. Natural Product Reports 22:15–61; doi: 10.1039/ b415080p. Brady, S.F., and J. Clardy. 2000. First discovery of a new biologically active molecule from eDNA: Long-chain N-acyl amino acid antibiotics isolated from heterologously expressed environmental DNA. Journal of the American Chemical Society 122:12,903–12,904. Brady, S.F., C.J. Chao, J. Handelsman, and J. Clardy. 2001. First isolation of the genes for a known molecule from eDNA: Cloning and heterologous expression of a natural product biosynthetic gene cluster from eDNA. Organic Letters 3:1,981–1,984. Clardy, J. 2005. A possibly useful review on marine natural products: Using genomics to deliver natu￾ral products from symbiotic bacteria. Genome Biology 6:232–236. Cragg, G.M., D.G.I. Kingston, and D.J. Newman, eds. 2005. Anticancer Agents from Natural Products. CRC Press/Taylor and Francis, Boca Raton, FL. Faulkner, D.J. 2000a. Marine natural products. Natural Products Reports 17:7-55; also see previous reviews beginning in 1984 ibid 1(3):251-280. Faulkner, D.J. 2000b. Highlights of marine natural products chemistry (1972–1999). Natural Products Reports 17:1–6. Hay, M.E. 1996. Marine chemical ecology: What’s known and what’s next? Journal of Experimental Marine Biology and Ecology 200(1–2):103–134. Hay, M.E. 2002. The next wave in aquatic chemical ecology. 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Discrimination between calcium channel subtypes using omega￾conotoxin from Conus magus venom. Biochemistry 26:2,086–2,090. Rao, K.V., N. Kasanah, S. Wahyuono, B.L. Tekwani, R.F. Schinazi, and M.T. Hamann. 2004. Three new manzamine alkaloids from a common Indonesian sponge and their activity against infectious and tropical parasitic diseases. Journal of Natural Prod￾ucts 67(8):1,314–1,318. Stach, J.E.M., and A.T. Bull. 2005. Estimating and comparing the diversity of marine actinobacteria. Antonie van Leeuwenhoek 87:3–9. Therapeutic Research Faculty. 2006. Natural Medicines Comprehensive Database. 2006. Prepared by the editors of Pharmacist’s Letter and Prescriber’s Let￾ter. Therapeutic Research Faculty, Stockton, CA, ISBN 0-9747062-4-8. [Online] Available at: http:// www.accp.com/th_06nmcd.php [last accessed April 6, 2006]. Venter, J.C., K. Remington, J.F. Heidelberg, A.L. Halp￾ern, D.D. Rusch, J.A. Eisen, D.-Y. Wu, I. Paulsen, K.E. Nelson, W. Nelson, D.E. Fouts, S. Levy, A.H. Knap, M.W. Lomas, K. Nealson, O. White, J. Pe￾terson, J. Hoffman, R. Parsons, H. Baden-Tillson, C. Pfannkoch, Y.H. Rogers, and H.O. Smith. 2004. Environmental genome shotgun sequencing of the Sargasso Sea. Science 304:66–74. Wratten, S.J., and D.J. Faulkner. 1977. Carbonimidic dichlorides from the marine sponge Pseudaxinyssa pitys. Journal of the American Chemical Society 99:7,367–7,368. Figure 10. A close-up underwater photo of the Indonesian sponge Acanthostrongylophora sp. Th is sponge contains complex molecules of the manzamine class (manzamine A shown). Th e manzamines, which show potent activity against human parasites, are thought to be produced by a bacterium found within the sponge. Photo courtesy M. Hamann, University of Mississippi, Oxford, Mississippi
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