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Review
. 2015 Mar 16;16(3):6018-56.
doi: 10.3390/ijms16036018.

The effects of marine carbohydrates and glycosylated compounds on human health

Affiliations
Review

The effects of marine carbohydrates and glycosylated compounds on human health

Hee-Kyoung Kang et al. Int J Mol Sci. .

Abstract

Marine organisms have been recognized as a valuable source of bioactive compounds with industrial and nutraceutical potential. Recently, marine-derived carbohydrates, including polysaccharides and low molecular weight glycosylated oligosaccharides, have attracted much attention because of their numerous health benefits. Moreover, several studies have reported that marine carbohydrates exhibit various biological activities, including antioxidant, anti-infection, anticoagulant, anti-inflammatory, and anti-diabetic effects. The present review discusses the potential industrial applications of bioactive marine carbohydrates for health maintenance and disease prevention. Furthermore, the use of marine carbohydrates in food, cosmetics, agriculture, and environmental protection is discussed.

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Figures

Figure 1
Figure 1
Predicted structure of MP-I (3), isolated from Mytilus coruscus [36].
Figure 2
Figure 2
Floridoside (10) and d-isofloridoside (11), isolated from the marine alga Laurencia undulata [42].
Figure 3
Figure 3
The structure of fucoidan (12) [46].
Figure 4
Figure 4
Aquastatin A (13), isolated from marine-derived fungus Cosmospora sp. SF-5060 [50].
Figure 5
Figure 5
The caminosides A–D (1619), isolated from the Caribbean marine sponge Chaetomorpha sphaeoroconia [54].
Figure 6
Figure 6
The novel triterpene glycoside (21), holothurin B (22) and holothurin A (23) isolated from sea cucumber Actinopyga lecanora [60].
Figure 7
Figure 7
Marmoratoside A (24), 17α-hydroxy impatienside A (25), marmoratoside B (26), and 25-acetoxy bivittoside D (27), isolated from sea cucumber Bohadschia marmorata [61].
Figure 8
Figure 8
Scabraside A (28), echinoidea A (29), and holothurin A1 (30), isolated from Holothuria scabra [62].
Figure 9
Figure 9
Sokodosides A (31) and B (32) isolated from marine sponge Erylus placenta [64].
Figure 10
Figure 10
Pandaroside G (48) and pandaroside G methyl ester (49), isolated from the sponge, Pandaros acanthifolium [78].
Figure 11
Figure 11
Acanthifoliosides A–F (5052) isolated from the sponge, Pandaros acanthifolium [79].
Figure 12
Figure 12
Glycosides 5663, isolated from octocoral, Muricea austere [82].
Figure 13
Figure 13
The d,l-galactan hybrid C2S-3 (69), isolated from the red seaweed Cryptonemia crenulata [88].
Figure 14
Figure 14
Sulfated polymannuroguluronate (SPMG, 73) isolated from brown algae Laminaria japonica [92].
Figure 15
Figure 15
Dermatan sulfate (79), isolated from ascidian Styela plicata [102].
Figure 16
Figure 16
Carijoside A (80), isolated from Carijoa sp. [103].
Figure 17
Figure 17
ASLP (83) isolated from Lischke Arca subcrenata [107].
Figure 18
Figure 18
HCLPS-1 (84) isolated from clam of Hyriopsis cumingii [108].
Figure 19
Figure 19
Frondoside A (85) isolated from sea cucumber Cucumaria frondosa [110].
Figure 20
Figure 20
Cucumariosides (especially most active glycoside cucumarioside A2-2, 86) isolated from sea cucumber Cucumaria japonica [116].

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