ライフサイエンスコーパス: marine sponge

1 ivated bacteria that exist as symbionts in a marine sponge.

2 sylceramide (alpha-GalCer), derived from the marine sponge.

3 enome report of a cultivated symbiont from a marine sponge.

4 tor (KAR) ligands originally isolated from a marine sponge.

5 pathway through symbiotic microorganisms of marine sponges.

6 stence of new structural classes of PBDEs in marine sponges.

7 nthetic bacteria associated with beetles and marine sponges.

8 potent anticancer agent originally found in marine sponges.

9 aryl-pyrazin-2-one core was derived from the marine sponge alkaloid family of hamacanthins.

10 The marine sponge alkaloid leucettamine B was recently ident

11 g found in fungi, vascular and lower plants, marine sponges and algae, and insects.

12 ated from terrestrial cyanobacteria and from marine sponges and gastropods.

13 tural products isolated from fungal species, marine sponges, and cactaceous species.

14 Marine sponges are major habitat-forming organisms in co

15 ether Shark Bay bottlenose dolphins that use marine sponges as hunting tools (spongers) are culturall

16 symbiosum found living in association with a marine sponge, Axinella mexicana.

17 These include glycolipids from a marine sponge, bacterial glycolipids, normal endogenous

18 n which lives in specific association with a marine sponge, belongs to a recently recognized nontherm

19 abilizing agent originally isolated from the marine sponge Cacospongia mycofijiensis.

20 66 was identified in a saline extract of the marine sponge, Callyspongia sp.

21 sing the axial cores of silica spicules in a marine sponge chemically and spatially direct the polyme

22 While no sulfated GAGs have been found in marine sponges, chondroitin sulfate (CS) and heparan sul

23 ed from a Papua New Guinea collection of the marine sponge Cinachyrella enigmatica.

24 ccharide fragment of the naturally occurring marine sponge clarhamnoside.

25 B (2) have been isolated from the Philippine marine sponge Clathria (Thalysias) abietina.

26 The marine sponge constituent aaptamine (1) has been convert

27 of such 1H-benzo[de][1,6]-naphthyridine (1) marine sponge constituents at position C-9 has been deve

28 anisms that are sessile or slow moving, some marine sponges contain aversive compounds that defend th

29 ion of NKT cells is greatly augmented by the marine sponge-derived glycolipid alpha-galactosylceramid

30 cells recognize glycolipid Ags, such as the marine sponge-derived glycosphingolipid alpha-galactosyl

31 Although presentation of the marine sponge-derived lipid alphaGalCer to type I NKT ce

32 iNKT cells with glycolipid Ags, such as the marine sponge-derived reagent alpha-galactosylceramide (

33 HLO) assay has been employed to discover new marine-sponge-derived bioactive compounds.

34 (+)-18-epi-latrunculol A, a congener of the marine-sponge-derived latrunculins A and B, is reported.

35 Because alpha-GalCer is a marine-sponge-derived ligand, our study here shows that

36 a pyrrole-imidazole alkaloid obtained from a marine sponge, exhibits potent in vitro activity against

37 sly identified from the silica skeleton of a marine sponge, for enzyme variants capable of synthesizi

38 en) derivatives are bioactive alkaloids from marine sponges found to induce Ca(2+) release from stria

39 The marine sponge glycolipid alpha-galactosylceramide (alpha

40 mpound, adociasulfate-2, was isolated from a marine sponge, Haliclona (also known as Adocia) species,

41 hamigeran diterpenoids from the New Zealand marine sponge Hamigera tarangaensis are described.

42 the glassy skeletal elements (spicules) of a marine sponge, has led to the development of new low-tem

43 e (alpha-GalCer), originally isolated from a marine sponge, has potent immunomodulatory activities in

44 We previously demonstrated that the marine sponge Hymeniacidon heliophila displayed signific

45 The marine sponge Ianthella basta synthesizes at least 25 te

46 adin-5, a brominated macro-dilactam from the marine sponge Ianthella basta, enhances release of Ca2+

47 de analogues from two taxonomically distinct marine sponges including two Auletta spp. and one Jaspis

48 Bacteria isolated from marine sponges, including the Silicibacter-Ruegeria (SR)

49 as cyclosporin A blocks tissue rejection in marine sponges indicates that the cellular mechanisms fo

50 Hemiasterlin, a tripeptide isolated from marine sponges, induces microtubule depolymerization and

51 nalog of a natural steroidal alkaloid from a marine sponge, inhibits Tat-mediated transactivation of

52 The Indo-Pacific marine sponge Ircinia ramosa has been found to contain t

53 a have been reported for the closely related marine sponges Ircinia fasciculata and Ircinia variabili

54 tionation of the crude methanol extract of a marine sponge, Ircinia sp., yielded tedanolide C (1), a

55 dermolide (DDM), a polyketide macrolide from marine sponge, is a potent microtubule assembly promoter

56 Laulimalide, a natural product from marine sponges, is a microtubule-stabilizing agent that

57 s an antimitotic macrolide isolated from the marine sponge Leiodermatium sp. whose potentially novel

58 stigation of a new species of the deep-water marine sponge Leiodermatium, collected by manned submers

59 irst total synthesis of the antiinflammatory marine sponge metabolite (+)-cacospongionolide B has bee

60 tal synthesis of the architecturally complex marine sponge metabolite (-)-enigmazole A has been achie

61 zepines that are structurally related to the marine sponge metabolite hymenialdisine.

62 We identified the marine sponge metabolite latonduine as a corrector.

63 e previously shown that ilimaquinone (IQ), a marine sponge metabolite, causes complete vesiculation o

64 The total syntheses of the antiinflammatory marine sponge metabolites (+)-cacospongionolide B and E

65 thesis and stereochemical elucidation of the marine sponge metabolites (4R,6R)-plakilactone C, (4R,6R

66 short synthesis of the hydantoin-containing marine sponge metabolites axinohydantoins is described.

67 A new asymmetric synthesis of these marine sponge metabolites is described herein, featuring

68 membrane-anchored epitopes derived from the marine sponge Microciona prolifera has been explored by

69 study tissue acceptance and rejection in the marine sponge Microciona prolifera.

70 Ruegeria sp. strain KLH11, isolated from the marine sponge Mycale laxissima, produces a complex profi

71 ide, a cytotoxic macrolide isolated from the marine sponge Neopeltidae.

72 Extracts of the marine sponge Niphates digitalis collected in Dominica s

73 ing potent antifungal activity reported from marine sponges of the genera Microscleroderma and Theone

74 codermolide, a promising anticancer agent of marine sponge origin, has been completed in 11.1% overal

75 , a 14-membered macrolides isolated from the marine sponge Phakellia fusca Thiele, which was collecte

76 oles B-F, were isolated from extracts of the marine sponge Phorbas amaranthus along with the known am

77 15), have been isolated from extracts of the marine sponge Phorbas sp. collected in Howe Sound Britis

78 olated in only 90 microg yield from the same marine sponge, Phorbas sp. that also provided phorboxazo

79 The family of silicatein enzymes from marine sponges (phylum Porifera) is unique in nature for

80 13 oxygenated polyketides isolated from the marine sponge Plakinastrella mamillaris allowed the disc

81 active fractions derived from the Australian marine sponge Plakortis lita .

82 Here, we document marine sponge presenting associated with visual and acou

83 d of using light or heat as a driving force, marine sponges promote cycloaddition with a more versati

84 A screening of marine sponges revealed that crude extracts of Psammocin

85 f the natural product rhizochalin C from the marine sponge Rhizochalina incrustata.

86 ound as a single gene in the horseshoe crab, marine sponge, sea urchin, nematode, and fruit fly, wher

87 Here, we report suvanine, a marine sponge sesterterpene, as an antagonist of the mam

88 opapuamides B-D, have been isolated from the marine sponge Siliquariaspongia mirabilis.

89 rins, mollenynes B-E, were isolated from the marine sponge Spirastrella mollis collected from Hogsty

90 e/2-propanol (1:1) extract of the Indonesian marine sponge Strepsichordaia aliena, twelve new 20, 24-

91 ro5-Tyr6-cis-Pro7]) isolated from the Fijian marine sponge Stylotella aurantium are reported.

92 re isolated from the n-hexane extract of the marine sponge Svenzea flava collected at Great Inagua Is

93 wo cyclic diarylheptanoids isolated from the marine sponge Tedania ignis.

94 ilicatein, an enzymatic biocatalyst from the marine sponge Tethya aurantia, is demonstrated to cataly

95 y connection in the skeletal elements of the marine sponge Tethya aurantia.

96 lectella aspergillum, is a sediment-dwelling marine sponge that is anchored into the sea floor by a f

97 miasterlin is a natural product derived from marine sponges that, like other structurally diverse pep

98 totheonella gemina" live associated with the marine sponge Theonella swinhoei Y, the source of numero

99 -inhabit the chemically and microbially rich marine sponge Theonella swinhoei.

100 w polyhydroxylated steroid isolated from the marine sponge Theonella swinhoei.

101 rization of conicasterol E isolated from the marine sponge Theonella swinhoei.

102 from 11 cultivated archaeal species and one marine sponge tissue sample that contained essentially a

103 Although this marine sponge toxin is known to inhibit protein phosphat

104 We report here that the marine sponge toxin, latrunculin B, which blocks photopo

105 Only adult males presented marine sponges, typically doing so in the presence of se

106 Pateamine A, a natural product isolated from marine sponge, was recently reported to inhibit eukaryot

107 d in the extracellular aggregation factor of marine sponges, which mediates species-specific cell agg

108 OH-XeA, and araguspongin C isolated from the marine sponge Xestospongia species also inhibit IP(3)-me

109 ) and B (7) were also isolated from the same marine sponge (Zyzzya sp.).