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Overview Bioactive Compounds from Sponges (Phylum Porifera) Diversity of Sponge-Derived Compounds Manoalide: A Phospholipase A2 Inhibitor Bioactive Compounds from Cnidarians Introduction to the Cnidaria Pseudoptersin: An Inhibitor of Eicosanoid Release Drugs from the Sea: Sponges Inhibits cell-division by stabilizing microtubules (i.e. inhibiting depolymerization) Anticancer drug Discodermia dissolute (Clinical Phase II) HO O O OH O NH2 O OH Discodermolide Drugs from the Sea: Sponges Halichondrin B Okadaic Acid Halichondria okadai H O H O O O O O H CH3 O O OH O H H O O O H O H O H3C O H HO H3C OH O OH O O CH3 O HO O O H H OH CH3 H H HO HO OA inhibits PP1 and PP2A sub-type of Ser/Thr Protein Phosphatases Biomedical Research Tool O O O Other Bioactive Compounds from Marine Sponges More than 5,300 sponge derived compounds (2000) …hundreds more discovered each year. Other Bioactive Compounds from Marine Sponges O R HN Arabinose HO O N R = CH3, Spongothymidine R = H, Spongouracil (from Cryptotethya crypta) O OH O CH 3 NH2 HN OH N HO HO O O N O N Retrovir® O OH OH Cytosine Arabinoside (Ara-C) N N+ N- Azothymidine (AZT), or Zidovudine Other Bioactive Compounds from Marine Sponges: Antiviral Antiviral Compounds from Sponges Compound Dragmacidin F Papuamides C, D Mololipids Haplosamates A, B Hamigeran B Weinbersterols A, B Variolin B Avarol “2’, 5’-A” Hennoxazole A Class Indole Alkaloid Cyclic Peptides Tyramine Lipids Sulfamated Steroid Phenolic Macrolide Sulfated Sterols Alkaloid Hydroquinone/ Sesquiterpene 2’,5’-Nucleotide Bisoxazole Activity Antiviral HIV-1 HIV-1 HIV-1 Integrase Inhibitor Antiviral - Herpes, Polio Antiviral - Feline Leukemia Antiviral UAG Suppressor Gln tRNA Inhibitor Interferon Mediator Antiviral Other Bioactive Compounds from Marine Sponges: Antimicrobial Compound Discodermins B, C, D TopsentiasterolSulfates Arenosclerins A, B , C Axinellamines B-D Acanthosterol I and J Oceanapiside Spongistatin Leucascandrolide A Class Cyclic Peptide Sulfated Sterol Alkylpiperidine Imidazo-azolo-imidazole alkaloid Sulfated Sterol Biasminohydroxylipid Glycoside Polyether Macrolide Lactone Oxazole-Containing Polyether Macrolide Activity Antibacterial Antibacterial/Antifungal Antibacterial Antibacterial Antifungal Antifungal Antifungal Antifungal Other Bioactive Compounds from Marine Sponges: “Antifouling” Compound Kalihinene X Kalihipyran B 10 b -Formarnidokalihinol Pseudoeratidine 2 Ceratinamide A and B C22 Ceramide Formoside Axynyssimides Class Isocyanoterpenoid Isocyanoterpenoid Isocyanoterpenoid Dibromopyrrole-Containing Spermidine Derivative Bromotyrosine Derivative Ceramide Triterpene Glycoside, Sterol Diperoxide Sesquiterpene Carbonimide Dichlorides Other Bioactive Compounds from Marine Sponges: Anticancer Compound BRS1 Isoaaptamine Debromohymenialdisine Adociasulfates Laulimalide Peloruside A Hemiasterlin Dictyostatin Spongistatin 1 Halichondrin B Arenastatin A Latrunculin A Neoamphimedine Elenic Acid Agelasphin Class Diamino-dihydroxypolyunsaturated lipid Benzonaphthyridine alkaloid Pyrrole-Guanidine Alkaloid Activity Protein Kinase C Inhibitor Triterpenoid Hydroquinone Macrocyclic Lactone Macrocyclic Lactone Tripeptide Macrocyclic Lactone Bis{spiroacetal} Macrolide Polyether Macrolide Macrocyclic Lactan/Lactone Thiazole Macrolide Pyridoacridine Alkaloid Kinesin Inhibitor Stabilization of Microtubules Stabilization of Microtubules Stabilization of Microtubules Stabilization of Microtubules Tubulin Polymerization Inhib. Tubulin Polymerization Inhib. Tubulin Polymerization Inhib. Actin-Depolymerization Topoisomerase II Inhibitor Alkylphenol a-Galactosylceramide Topoisomerase II Inhibitor NKT Cell Activator Protein Kinase C Inhibitor Protein Kinase C Inhibitor Other Bioactive Compounds from Marine Sponges: Antiinflammatory Compound Manoalide Dysidotronic Acid Ircinin-1 and -2 Petrosaspongiolides Spongidines A-d Topsentin Scalaradial Cacospongionolide B Jaspaquinol Subersic Acid Class Cyclohexane Sesterterpenoid Drimane Sesquiterpenoid Acyclic Sesterterpenoid Cheilantane Pyridinium Alkaloid Bis-Indole Alkaloid Scalarane Sesterterpene Sesterterpene Lactone Diterpene Benzenoid Diterpene Benzenoid Mode of Action Phospholipase A2 Inhibitor Phospholipase A2 Inhibitor Phospholipase A2 Inhbitor Phospholipase A2 Inhibitor Phospholipase A2 Inhibitor Phospholipase A2 Inhibitor Phospholipase A2 Inhibitor Phospholipase A2 Inhibitor Lipoxygenase Inhibitor Lipoxygenase Inhibitor Discovery of Manoalide Luffariella variabilis HO O O Manoalide O HO Antiinflammatory Assays Inflammation Assays (in vivo): e.g. Phorbol Myristate Acetate (PMA)-Induced Mouse Ear Edema PLA2 Assays (in vitro): Exogenous PLA2 - e.g. bee venom, cobra venom Phospholipids in Cell Membrane Phospholipids R2 O H2C O R1 O CH O H2C O O P O X O- R2 O H2C O O CH O Arachidonate O H2C O P O- O X Phospholipase-A2 (PLA2) Hydrolyzes Phospholids at sn-2 Position R2 O H2C O O CH O O H2C O P O X O- PLA2 R2 O H2C O COOH HO CH O H2C O Arachidonic Acid P O X O- Lysophospholipid Catalytic Mechanism of PLA2 Free Arachidonic Acid is Substrate for Eicosanoid Pathway Arachidonic Acid COOH Cyclooxygenases-1 and -2 (COX-1 and -2) Lipoxygenases (LOX) O OH COOH COOH HO OH OH OH Prostagalandin A2 (e.g.) Leukotriene B4 (e.g.) COO- HO O OH Thromboxane B2 (e.g.) Eicosanoid Release Triggers Inflammation Response Inflammation Response in Wound Healing Antiinflammatory Assays Inflammation Assays (in vivo): e.g. Phorbol Myristate Acetate (PMA)-Induced Mouse Ear Edema PLA2 Assays (in vitro): Exogenous PLA2 - e.g. bee venom, cobra venom Bee Venom Assay for PLA2 Activity 3H-Labeled Dipalmitoyl Phosphatidyl Choline O 3 H O 3H CH2 3H 3H 3H O CH CH3 3H O H2 C N+ O O P O O- PLA2 from Bee Venom 3 H 3 H 3 H OH 3H-Labeled Palmitic Acid Radioassay O CH3 CH3 Manoalide Inhibits PLA2 Activity of Bee Venom Reynolds et al. (1991) J. Biol. Chem., 266: 16512-7 Manoalide Irreversibly Inhibits PLA2 R2 O H2C O O CH O O H2C O P O X O- PLA2 R2 O H2C O COOH HO CH O H2C O Arachidonic Acid P O X O- Lysophospholipid Ring-Opening of Manoalide Creates Binding Sites HO O O O HO OH O HO O O CH CH Michael Addition OH O HO OH O CH CH O Schiff’s Base O O O OH Amide Manoalide Binds Lysine Residues in PLA2 HO O O O HO HO O O CH OH N Lys OH O CH CH N N Lys Lys OH Commerical Potential of Manoalide Licensed by Allergan® Pharmaceuticals Phase-I Clinical Trials for Treatment of Psoriasis Commercially Available Probe for PLA2 Drugs from the Sea: Cnidaria Phylum Cnidaria Class Anthozoa “Sea Pens” “Corals” “Sea Fans” Coral Biology Corals are FOUNDATION of reefs Zooxanthellae = Symbiotic algae in coral Planula Coral Diseases “Bleaching” “Tolerant” Susceptible Microbial Infection Bioactive Compounds Bioactive Compounds from Cnidarians: Pseudopterosin PsA PsB PsC PsD Pseudopterogorgia elisabethae (“Purple Sea Whip”) O R1O OH R1=R2=R3=H R1=Ac, R2=R3=H R2=Ac, R1=R3=H R3=Ac, R1=R2=H O OR3 R2O Look, Fenical, Jacobs and Clardy (1986) Proc. Natl. Acad. Sci., 83: 6238-40 Pseudopterosin A Inhibits Inflammation Response in Mouse Model O HO OH O OH HO Pseudopterosin A Look, Fenical, Jacobs and Clardy (1986) Proc. Natl. Acad. Sci., 83: 6238-40 Pseudopterosin A and E (PsA and PsE): Antiinflammatory Mechanism(s) O HO OH OH O OH O HO OH Pseudopterosin A OH O Pseudopterosin E Mayer et al. (1998) Life Sci., 62: 401-407 OH PsA and PsE Inhibit Mouse Ear Edema Mayer et al. (1998) Life Sci., 62: 401-407 PsA and PsE Inhibit PBQ- and ZymosanInduced Writhing Mayer et al. (1998) Life Sci., 62: 401-407 PsE Inhibits Zymosan-Induced Peritoneal Prostaglandin and Leukotriene Exudate Mayer et al. (1998) Life Sci., 62: 401-407 PsA and PsE Inhibit Zymosan-Induced Release of Prostaglandin and Leukotriene from Murine Peritoneal Macrophages Mayer et al. (1998) Life Sci., 62: 401-407 Commerical Potential of Pseudopterosins Licensed to OsteoArthritis Sciences, Inc. Synthetic Derivative (Methopterosin) Completed Pre-Clinical Trials; Expected to Enter Phase-1 Clinical Trials as Topical AntiInflammatory for Dermatitis Cosmetic Ingredient Pseudopterosins PsA PsB PsC PsD O R1O R1=R2=R3=H R1=Ac, R2=R3=H R2=Ac, R1=R3=H R3=Ac, R1=R2=H Seco-PsA Seco-PsB Seco-PsC Seco-PsD O O R1O OR3 R2O OH OH OH PsF R1=R2=R3=H R1=Ac, R2=R3=H R2=Ac, R1=R3=H R3=Ac, R1=R2=H O OR3 R2O OH O PsY OH O Seco-PsJ O O O HO O HO HO HO HO OH HO OH OH Terpenoid Biosynthesis ATP OH ADP ATP ADP O OH O COO- COO- HO -O P Mevalonate O P O- O O- 5-Phosphomevalonate “Isoprene” O -O P O- O O P O + O O- H O P O- P O O- Isopentyl Diphosphate -O -O O O O- Dimethylallyl Diphosphate O O P P O- O Geranyl Diphosphate Terpenoid Biosynthesis O -O P O- O O P O- O Geranyl Diphosphate OH Limonene Menthol Monoterpenoids (C-10) Terpenoid Biosynthesis O -O P O- O O O P O- + O -O P O- H O O P O- Isopentyl Diphosphate (IPP) Farnesyl Diphosphate O -O P O- O O P O- O O Geranyl Diphosphate Terpenoid Biosynthesis O -O P O- O O O P + O O- -O P O O O- H P O- O Geranyl Diphosphate Isopentyl Diphosphate (IPP) Farnesyl Diphosphate O O “Steroids” (C-30) -O P O P O O- O- Triterpenoids (C-30) Zingiberene Squalene Sesquiterpenoids (C-15) HO Lanosterol Terpenoid Biosynthesis O -O P O O O P O- + O O- -O P O- H O O P O- O Geranyl Diphosphate Isopentyl Diphosphate (IPP) Farnesyl Diphosphate O -O P O- O -O P O- O O P O- O O O P O- O + IPP Terpenoid Biosynthesis O -O P O O O P O- + O O- -O P O- H O O P O- O Geranyl Diphosphate Isopentyl Diphosphate (IPP) Farnesyl Diphosphate O -O P O- O -O P O- O O P O- O + IPP O O P O O- Diterpenoids (C-20) (-)-Kaurene Terpenoid Biosynthesis O -O P O O O P O- + O O- -O P O- H O O P O Geranyl Diphosphate O- Isopentyl Diphosphate (IPP) Farnesyl Diphosphate O -O P O- O -O P O- O O P O- O + IPP O O P O O- + IPP O -O P O- O O P O O- Sesterterpenoids (C-25) Manoalide is a Sesterterpene HO O O O HO Biosynthesis of Pseudopterosins Elisabethatriene H Erogorgiaene H H OPP GGPP H H H H OH OH OH HO OH OH O O O HO HO O HO OH OH