about
Bromopyrrole alkaloids as lead compounds against protozoan parasitesMumijo traditional medicine: fossil deposits from antarctica (chemical composition and beneficial bioactivity)Potent antioxidant and genoprotective effects of boeravinone G, a rotenoid isolated from Boerhaavia diffusaPalytoxin and an Ostreopsis toxin extract increase the levels of mRNAs encoding inflammation-related proteins in human macrophages via p38 MAPK and NF-κBNew insights on cytological and metabolic features of Ostreopsis cf. ovata Fukuyo (Dinophyceae): a multidisciplinary approach.Skin lipid structure controls water permeability in snake molts.Artarborol, a nor-caryophyllane sesquiterpene alcohol from Artemisia arborescens. stereostructure assignment through concurrence of NMR data and computational analysis.Spirolide toxin profile of Adriatic Alexandrium ostenfeldii cultures and structure elucidation of 27-hydroxy-13,19-didesmethyl spirolide C.Cold stress defense in the freshwater sponge Lubomirskia baicalensis. Role of okadaic acid produced by symbiotic dinoflagellates.LC-MS of palytoxin and its analogues: State of the art and future perspectives.ADP-ribosyl cyclases generate two unusual adenine homodinucleotides with cytotoxic activity on mammalian cellsNonprenylated rotenoids, a new class of potent breast cancer resistance protein inhibitors.Polyhydroxylated sterols from the Indonesian soft coral Sinularia sp. and their effect on farnesoid X-activated receptor.Manadoperoxides, a new class of potent antitrypanosomal agents of marine origin.Okadaic acid, an apoptogenic toxin for symbiotic/parasitic annelids in the demosponge Suberites domunculaCytotoxic Activity of Crude Extracts as well as of Pure Components from Jatropha Species, Plants Used Extensively in African Traditional MedicineToxin levels and profiles in microalgae from the north-Western Adriatic Sea--15 years of studies on cultured speciesChemical diversity of bioactive marine natural products: an illustrative case study.Marine antimalarials.The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism.A 4-decade-long (and still ongoing) hunt for palytoxins chemical architecture.Putative palytoxin and its new analogue, ovatoxin-a, in Ostreopsis ovata collected along the Ligurian coasts during the 2006 toxic outbreak.A new class of antimalarial dioxanes obtained through a simple two-step synthetic approach: rational design and structure-activity relationship studies.Zorrimidazolone, a bioactive alkaloid from the non-indigenous mediterranean stolidobranch Polyandrocarpa zorritensis.Spirocurcasone, a diterpenoid with a novel carbon skeleton from Jatropha curcas.Terpioside B, a difucosyl GSL from the marine sponge Terpios sp. is a potent inhibitor of NO release.Iodocionin, a cytotoxic iodinated metabolite from the Mediterranean ascidian Ciona edwardsii.Synthesis of structurally simplified analogues of aplidinone A, a pro-apoptotic marine thiazinoquinone.Clotrimazole scaffold as an innovative pharmacophore towards potent antimalarial agents: design, synthesis, and biological and structure-activity relationship studies.Clavaminols A-F, novel cytotoxic 2-amino-3-alkanols from the ascidian Clavelina phlegraea.Design and synthesis of potent antimalarial agents based on clotrimazole scaffold: exploring an innovative pharmacophore.Discovery and biological evaluation of the novel naturally occurring diterpene pepluanone as antiinflammatory agent.Novel bioactive bromopyrrole alkaloids from the Mediterranean sponge Axinella verrucosa.Cytotoxic germacrane sesquiterpenes from the aerial parts of Santolina insularis.Antitumor effects of two novel naturally occurring terpene quinones isolated from the Mediterranean ascidian Aplidium conicum.Structure-activity relationships for euphocharacins A-L, a new series of jatrophane diterpenes, as inhibitors of cancer cell P-glycoprotein.Yessotoxin, a shellfish biotoxin, is a potent inducer of the permeability transition in isolated mitochondria and intact cells.Jatrophane diterpenes as modulators of multidrug resistance. Advances of structure-activity relationships and discovery of the potent lead pepluanin A.Aplidiasterols A and B, two new cytotoxic 9,11-secosterols from the Mediterranean ascidian Aplidium conicum.Modified jatrophane diterpenes as modulators of multidrug resistance from Euphorbia dendroides L.
P50
Q24632744-ABBDE8E9-152C-4414-9784-9E51343EB041Q28300360-74970EBE-F045-4ED2-A15B-A2E47B62EF28Q28478207-2D1AC221-83ED-4B95-82F6-D3C4EDA874FEQ28484073-96442CEB-AD6F-423B-9828-3B69E18B9913Q28487041-8A4C3423-3A34-495B-9C85-35BE6553F87BQ30683749-591EA8EF-78AA-4700-A8FD-36490E03A02EQ31112019-507B936A-5273-447E-A07F-AB179D1DE89DQ31136512-C0E3BF0B-9B99-4F1B-843D-52AEC1EDFE45Q33269172-32D20492-FE78-4454-A321-73BFC378093AQ33744632-B1BE53A1-D86F-41B0-BC8E-88EE1F38D60BQ34000505-51DFA636-89B8-429F-B4FC-A2014520DA0EQ34002798-4769977C-DA0D-43CA-8FE5-AC9B0C174D52Q34129786-8039D46B-EA1D-479C-9D8F-10C6D285FB0AQ34363517-83ABD443-2BF4-4D5E-A515-25EF5CAC2A40Q34719124-83D76300-222B-4360-BCF6-AF7E0E7B64F4Q35094196-EC68CF9E-2612-41C3-AA32-B2515A096357Q35759927-D9B17149-14D4-4279-9007-9A117EEE321EQ35848132-BFCB960A-7D2D-4FD4-8002-0D3A266736F3Q37253569-7E368DA7-B855-4BF0-8FAF-5D233A2505ABQ37739450-66A3EFA0-D91D-4A16-AB92-B7AFF82C89A2Q38947517-0744762B-92EF-4D49-AEF7-FE7A05DE4737Q38947521-2DF6F8E3-09F9-47DA-9B93-7FB83167E052Q39447965-93D50EC6-34ED-4628-9FC1-F191AC414425Q39508549-6CE2BFB9-08FC-41DC-B0FD-B99D668FF3A7Q39622526-798FA87A-820A-44D3-B51D-4A158CF8E332Q39681273-744342B2-EBE0-4268-9FDD-F0544DD60F79Q39715086-6251162A-7692-45A0-B0A5-C90C948FEE8DQ39759700-BA5B7B30-096C-4E50-BCEB-3F9F241A231CQ40012667-C5EBF528-078E-43AD-B94D-70D561742291Q40163544-B37F78EE-2C5E-441B-AD77-7DF9A083A929Q40177378-2A9DB7B5-1118-4F1B-986F-CC39BF65B5D2Q40357834-214D282B-12CC-4915-9875-C33804E110B6Q40372097-160CF178-9BFF-4D49-83FD-405DFF19920AQ40405757-F6B972D8-1E69-4D18-9F08-E29A9CFAFACEQ40430071-8E756675-16A2-4E81-AE47-75F45C516DEFQ40535319-E584117F-564E-4762-9ACF-8160F87ECA4CQ40548988-E2D40949-A5F7-4A41-9180-91DF70AFFEACQ40592854-321B9F74-CC2D-4AAB-848E-D5BC0DA96661Q40615550-5FB74DC9-1E10-457D-891F-DC79A34CE0EFQ40618873-FA314FCD-3A6F-4162-90BD-9E68BE60CB62
P50
name
Ernesto Fattorusso
@en
type
label
Ernesto Fattorusso
@en
prefLabel
Ernesto Fattorusso
@en