Table 2.
Drug class | Compound/organisma | Chemistry | Pharmacological activity | IC50b | MMOAc | Countryd | References |
---|---|---|---|---|---|---|---|
Anti-inflammatory | Ascidiathiazones A (75) and B (76)/ascidian | Alkaloidg | Human neutrophil free radical inhibition in vitro and in vivo | 0.44–1.55 μM | Superoxide anion inhibition | NZL | (Pearce et al., 2007a) |
Anti-inflammatory | Crassumolides A and C (77, 78)/soft coral | Terpenoide | Modulation of LPS-activated murine macrophage cell line | < 10 μM | Inducible NOS and COX-2 inhibition | TAIW | (Chao et al., 2008) |
Anti-inflammatory | Durumolides A-C (79, 80, 81)/soft coral | Terpenoide | Modulation of LPS-activated murine macrophage cell line | < 10 μM | Inducible NOS and COX-2 inhibition | TAIW | (Cheng et al., 2008) |
Anti-inflammatory | Frajunolides B and C (82, 83)/coral | Terpenoide | Human neutrophil free radical inhibition in vitro | > 10 μg/mL⁎ | Superoxide anion and elastase inhibition | TAIW | (Shen et al., 2007) |
Anti-inflammatory | Gracilaria verrucosa fatty acids (84, 85)/alga | Polyketided | Modulation of LPS-activated murine macrophages in vitro | < 20 μg/mL⁎ | NO, IL-6 and TNF-α inhibition | S. KOR | (Dang et al., 2008) |
Anti-inflammatory | Hypnea cervicornis lectin (86)/alga | Peptideg | Antinociception and anti-inflammatory effects in vivo | 0.1–1 mg/kg⁎ | Carbohydrate-binding site interaction | BRA | (Bittencourt Fda S. et al., 2008) |
Anti-inflammatory | Manzamine (MZA) (87), (–)-8-hydroxy MZA (88), hexahydro-8-hydroxy MZA (89)/sponge | Alkaloidg | Modulation of LPS-activated brain microglia in vitro | 0.25–1.97 μM | TXB2 inhibition | USA | (El Sayed et al., 2008) |
Anti-inflammatory | ω-3 PUFA (90, 91, 92, 93)/mussel | Polyketided | Human neutrophil lipoxygenase inhibition in vitro | ND | LTB4 and 5-HETE inhibition | AUS | (Treschow et al., 2007) |
Anti-inflammatory | Perithalia capillaris quinone (94)/alga | Shikimate | Human neutrophil free radical release inhibition in vitro | 2.1 μM | Superoxide anion inhibition | NZL | (Sansom et al., 2007) |
Anti-inflammatory | PFF-B (95)/alga | Polyketided | Rat basophilic leukemia cell histamine release inhibition | 7.8 μM | Inhibition of β-hexosaminidase release | JPN | (Sugiura et al., 2007) |
Anti-inflammatory | Plakortide P (54)/sponge | Polyketidee | Modulation of LPS-activated brain microglia in vitro | 0.93 μM | TXB2 inhibition | BRA | (Kossuga et al., 2008) |
Anti-inflammatory | Rubrolide O (96)/ascidian | Polyketided | Human neutrophil free radical release inhibition in vitro | 35 μM | Superoxide anion inhibition | NZL | (Pearce et al., 2007b) |
Anti-inflammatory | Stearidonic (97)/alga | Polyketided | Inhibition of mouse ear inflammation | 160–314 μg/ear | Inhibition of edema, erythema and blood flow | S. KOR, JPN | (Khan et al., 2007) |
Anti-inflammatory | Carteramine A (98)/sponge | Alkaloidg | Neutrophil chemotaxis inhibition | 5 μM | Undetermined | JPN | (Kobayashi et al., 2007a) |
Anti-inflammatory | Lyngbyastatins 5–7 (99, 100, 101)/bacterium | Peptideg | Elastase inhibition | 3–10 nM | Undetermined | USA | (Taori et al., 2007) |
Anti-inflammatory | Salinipyrone A (102)/bacterium | Polyketidee | Mouse splenocyte interleukin-5 inhibition | 10 μg/mL | Undetermined | USA | (Oh et al., 2008) |
Immune system | Cycloprodigiosin hydrochloride (103)/bacterium | Alkaloidg | Interleukin-8 inhibition | 1 μM | AP-1 transcription factor inhibition | JPN | (Kawauchi et al., 2007) |
Immune system | Floridoside (104)/alga | Sugarh | Activation of classical complement pathway | 5.9–9.3 μg/mL⁎ | IgM mediated-effect | FRA | (Courtois et al., 2008) |
Immune system | Iantherans (105, 106)/sponge | Polyketided | Activation of Ca2+-mobilization | 0.48–1.3 μM | Ionotropic P2Y11 receptor activation | DEU, USA | (Greve et al., 2007) |
Immune system | Prodigiosin (107)/bacterium | Alkaloidg | Macrophage iNOS inhibition | 0.1 μg/mL⁎ | NF-κB transcription factor inhibition | S. KOR | (Huh et al., 2007) |
Immune system | ASLP (108)/clam | Polysaccharideh | Splenocyte proliferation increase | < 100 μg/mL⁎ | Undetermined | CHN | (He et al., 2007) |
Immune system | Frondoside A (109)/sea cucumber | Terpenoid glycoside | Lysosomal activity, phagocytosis and ROS activation | 0.1–0.001 μg/mL | Undetermined | RUS, USA | (Aminin et al., 2008) |
Immune system | Hippospongia sp. quinones (110, 111, 112)/sponge | Terpenoidf | Enhancement of IL-8 release | > 1 μg/mL⁎ | Undetermined | JPN | (Oda et al., 2007) |
Immune system | Macrosphelide M (113)/fungus | Polyketided | Cell adhesion inhibition | 33.2 μM | Undetermined | JPN | (Yamada et al., 2007) |
Immune system | Peribysin J (114)/fungus | Terpenoidf | Cell adhesion inhibition | 11.8 μM | Undetermined | JPN | (Yamada et al., 2007) |
Immune system | Querciformolide C (115)/soft coral | Terpenoidf | Macrophage iNOS and COX-2 inhibition | < 10 μM⁎ | Undetermined | TAIW | (Lu et al., 2008) |
Immune system | Spongia sp. diterpenoids (116, 117)/sponge | Terpenoidf | Murine spleen cell lysosome activation | > 100 μg/mL⁎ | Undetermined | RUS | (Ponomarenko et al., 2007) |
Immune system | Thalassospiramide B (118)/bacterium | Peptideg | Interleukin 5 inhibition | 5 μM | Undetermined | USA | (Oh et al., 2007) |
Nervous system | Linckosides L1 and L2 (119, 120)/sea star | Triterpenoid glycosidef | Induction of neurite outgrowth | 0.3 μM⁎ | Undetermined | ITA, RUS | (Kicha et al., 2007b) |
Nervous system | Linckosides M–Q (121, 122, 123, 124, 125)/sea star | Triterpenef | Induction of neurite outgrowth | < 10 μM⁎ | Dependent on xylose on side chain | JPN | (Han et al., 2007) |
Nervous system | Phaeophytin A (126)/alga | Alkaloid/terpenoid | Induction of neurite outgrowth | < 3.9 μM⁎ | MAP kinase activation | JPN | (Ina et al., 2007) |
Nervous system | Conus leopardus conotoxin Lp1.1 (127)/snail | Peptideg | Seizure and paralysis in goldfish | < 10 μM⁎ | Slow block of α6α3β2 and α3β2 nicotinic receptor | CHN, USA | (Peng et al., 2008) |
Nervous system | Damipipecolin (128) and damituricin (129)/sponge | Alkaloidg | Inhibition of serotonin receptor binding | 1 μg/mL⁎ | Ca2+ influx inhibition | ITA, DEU | (Aiello et al., 2007) |
Nervous system | 4-Acetoxy-plakinamine B (130)/sponge | Triterpenoid alkaloidg | Acetylcholinesterase inhibition | 3.75 μM | Mixed-competitive inhibition | THAI | (Langjae et al., 2007) |
Nervous system | Sargaquinoic acid (131) and sargachromenol (132)/alga | Terpenoidf | Butyrylcholinesterase inhibition | 26 nM | Undetermined | S. KOR | (Choi et al., 2007) |
Nervous system | SPMG (74)/alga | Polysaccharideh | Neuronal Ca2+-apoptosis inhibition | Decrease in caspase-3 activity | CHN | (Hui et al., 2008) |
aOrganism: Kingdom Animalia: coral (Phylum Cnidaria); ascidian (Phylum Chordata), sea star, cucumber (Phylum Echinodermata); clam, musse, snail (Phylum Mollusca); sponge (Phylum Porifera); Kingdom Fungi: fungus; Kingdom Plantae: alga; Kingdom Monera: bacterium (Phylum Cyanobacteria); bIC50: concentration of a compound required for 50% inhibition; *: apparent IC50; ND: not determined; cMMOA: molecular mechanism of action, NO: nitric oxide; dCountry: AUS: Australia; BRA: Brazil; CHN: China; DEU: Germany; FRA: France; ITA: Italy; JPN: Japan; NZL: New Zealand; RUS: Russia; S. KOR: South Korea; TAIW: Taiwan; THAI: Thailand; Chemistry: epolyketide; fterpene; gnitrogen-containing compound; hpolysaccharide, modified as in the text.