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Cytotoxic Polyketide Derivatives from the South China Sea Sponge Plakortis simplex
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
inferredcites →https://doi.org/10.1016/0040-4020(95)00856-xopenalex-snapshot
The plakortones, novel bicyclic lactones from the sponge Plakortis halichondrioides: Activators of cardiac SR-Ca2+-pumping ATPase
inferredcites →https://doi.org/10.1016/j.tet.2005.09.077openalex-snapshot
New bioactive cyclic peroxides from the Caribbean marine sponge Plakortis zyggompha
inferredcites →https://doi.org/10.1016/j.tet.2012.04.025openalex-snapshot
Simplexolides A–E and plakorfuran A, six butyrate derived polyketides from the marine sponge Plakortis simplex
inferredcites →https://doi.org/10.1016/j.tetlet.2005.09.011openalex-snapshot
Stereocontrolled synthesis of (±)-methyl 3,6-epoxy-4,6,8-triethyl-2,4,9-dodecatrienoate, a major metabolite of Caribbean sponge, Plakortis halichondrioides, using reactions of alkylidenecarbenes in one pot
inferredcites →https://doi.org/10.1021/ja9727225openalex-snapshot
Glycolipids from Sponges. 6.1 Plakoside A and B, Two Unique Prenylated Glycosphingolipids with Immunosuppressive Activity from the Marine Sponge Plakortis simplex
inferredcites →https://doi.org/10.1021/jm060899gopenalex-snapshot
Endoperoxide Derivatives from Marine Organisms: 1,2-Dioxanes of the Plakortin Family as Novel Antimalarial Agents
inferredcites →https://doi.org/10.1021/jm800791fopenalex-snapshot
Directed Discovery of Agents Targeting the Met Tyrosine Kinase Domain by Virtual Screening
inferredcites →https://doi.org/10.1021/jo200637gopenalex-snapshot
Vicinal 1H–1H NMR Coupling Constants from Density Functional Theory as Reliable Tools for Stereochemical Analysis of Highly Flexible Multichiral Center Molecules
inferredcites →https://doi.org/10.1021/np000413dopenalex-snapshot
Three New Furan Derivatives and a New Fatty Acid from a Taiwanese Marine Sponge Plakortis simplex
inferredcites →https://doi.org/10.1021/np020589aopenalex-snapshot
Three New Cyclic Peroxides from the Marine Sponge Plakortis aff simplex
inferredcites →https://doi.org/10.1021/np030358jopenalex-snapshot
New Cytotoxic Metabolites from a Marine Sponge Homaxinella sp.
inferredcites →https://doi.org/10.1021/np049665vopenalex-snapshot
Cyclic Peroxides Derived from the Marine Sponge Plakortis simplex
inferredcites →https://doi.org/10.1021/np100196bopenalex-snapshot
Manadoperoxides A−D from the Indonesian Sponge Plakortis cfr. simplex. Further Insights on the Structure−Activity Relationships of Simple 1,2-Dioxane Antimalarials
inferredcites →https://doi.org/10.1021/np200487kopenalex-snapshot
Cyclic Ether-Containing Macrolactins, Antimicrobial 24-Membered Isomeric Macrolactones from a Marine Bacillus sp.
inferredcites →https://doi.org/10.1021/np200693zopenalex-snapshot
Absolute Structures of Monoterpenoids with a δ-Lactone-Containing Skeleton from Ligularia hodgsonii
inferredcites →https://doi.org/10.1021/np50102a023openalex-snapshot
Four New C16 1,2-Dioxene-polyketides from the Sponge Plakortis aff. simplex
inferredcites →https://doi.org/10.1021/np9705118openalex-snapshot
A Bioactive Secosterol with an Unusual A- and B-Ring Oxygenation Pattern Isolated from an Indonesian Soft Coral Lobophytum sp.
inferredcites →https://doi.org/10.1021/ol201055wopenalex-snapshot
Simplextones A and B, Unusual Polyketides from the Marine Sponge Plakortis simplex
inferredcites →https://doi.org/10.1590/s0103-50532005000800010openalex-snapshot
Polyketides from the marine sponge Plakortis angulospiculatus
inferredcites →https://doi.org/10.3390/md10051027openalex-snapshot
Woodylides A–C, New Cytotoxic Linear Polyketides from the South China Sea Sponge Plakortis simplex
inferredcites →https://doi.org/10.3987/rev-04-sr(p)1openalex-snapshot
Metabolites from Marine Sponges of the Genus Plakortis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4466.1.4zenodo-depositor-declared
New sciaphilic plakinids (Porifera, Homoscleromorpha) from the Central-Western Pacific
inferred← citeshttps://doi.org/10.1002/9781119143802.ch115openalex-snapshot
Cytotoxic and Antitumor Compounds from Marine Invertebrates
inferred← citeshttps://doi.org/10.1002/ange.201913130openalex-snapshot
Nickel(0)‐Catalyzed Enantioselective [3+2] Annulation of Cyclopropenones and α,β‐Unsaturated Ketones/Imines
inferred← citeshttps://doi.org/10.1002/ange.202015232openalex-snapshot
Unified Approach to Furan Natural Products via Phosphine‐Palladium Catalysis
inferred← citeshttps://doi.org/10.1002/ange.202109266openalex-snapshot
Indium‐katalysierte Transferhydrierung zur reduktiven Cyclisierung von 2‐Alkinylenonen zu trisubstituierten Furanen
inferred← citeshttps://doi.org/10.1002/anie.201913130openalex-snapshot
Nickel(0)‐Catalyzed Enantioselective [3+2] Annulation of Cyclopropenones and α,β‐Unsaturated Ketones/Imines
inferred← citeshttps://doi.org/10.1002/anie.202015232openalex-snapshot
Unified Approach to Furan Natural Products via Phosphine‐Palladium Catalysis
inferred← citeshttps://doi.org/10.1002/anie.202109266openalex-snapshot
Indium‐Catalysed Transfer Hydrogenation for the Reductive Cyclisation of 2‐Alkynyl Enones towards Trisubstituted Furans
inferred← citeshttps://doi.org/10.1002/chem.202402688openalex-snapshot
Spirocyclopropanes and Substituted Furans by Controlling Reactivity of 1,3‐Enynoates: γ‐ and δ‐Addition of Phosphines to Conjugate Acceptors
inferred← citeshttps://doi.org/10.1002/ejoc.202501191openalex-snapshot
Bis‐Furans: A Sustainable Source of Diverse Molecular Architectures
inferred← citeshttps://doi.org/10.1007/978-3-319-07145-9_3openalex-snapshot
Marine Sponge Derived Antiangiogenic Compounds
inferred← citeshttps://doi.org/10.1007/s00216-021-03385-6openalex-snapshot
Metabolomic fingerprinting of Brazilian marine sponges: a case study of Plakinidae species from Fernando de Noronha Archipelago
inferred← citeshttps://doi.org/10.1007/s10593-023-03224-9openalex-snapshot
Synthesis of 2-hexyl-5-ethylfuran-3-sulfonic acid (HEFS) – natural antithrombosis agent from Eisenia earthworms
inferred← citeshttps://doi.org/10.1007/s42995-022-00132-3openalex-snapshot
Chemical and biological diversity of new natural products from marine sponges: a review (2009–2018)
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01218openalex-snapshot
Organocatalyzed Synthesis of γ-Alkenyl Butenolides via Asymmetric Direct Vinylogous Conjugate Addition–Elimination of Substituted Furanone Derivatives to β-Phenylsulfonylenones
inferred← citeshttps://doi.org/10.1021/acs.joc.6b00695openalex-snapshot
PPAR Modulating Polyketides from a Chinese Plakortis simplex and Clues on the Origin of Their Chemodiversity
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c01957openalex-snapshot
Rhodium-Catalyzed Sequential Cycloisomerization/Aldol Addition of Cyclopropene Carboxylic Acids with Isatins
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03751openalex-snapshot
Access to Bromo-γ-butenolides via Zwitterion-Catalyzed Rearrangement of Cyclopropene Carboxylic Acids
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b01503openalex-snapshot
(+)- and (−)-Spiroreticulatine, A Pair of Unusual Spiro Bisheterocyclic Quinoline-imidazole Alkaloids from the South China Sea Sponge Fascaplysinopsis reticulata
inferred← citeshttps://doi.org/10.1021/acscatal.7b00590openalex-snapshot
Highly Efficient Asymmetric Synthesis of Chiral γ-Alkenyl Butenolides Catalyzed by Chiral N,N′-Dioxide–Scandium(III) Complexes
inferred← citeshttps://doi.org/10.1021/ja406356copenalex-snapshot
Enantioselective α-Alkenylation of Aldehydes with Boronic Acids via the Synergistic Combination of Copper(II) and Amine Catalysis
inferred← citeshttps://doi.org/10.1021/np500249vopenalex-snapshot
Cycloartane Triterpenoids and Their Glycosides from the Rhizomes of Cimicifuga foetida
inferred← citeshttps://doi.org/10.1021/ol403625gopenalex-snapshot
Alistonitrine A, a Caged Monoterpene Indole Alkaloid from Alstonia scholaris
inferred← citeshttps://doi.org/10.1039/c4ob00145aopenalex-snapshot
Cooperative N-heterocyclic carbene (NHC)–Lewis acid-mediated regioselective umpolung formal [3 + 2] annulations of alkynyl aldehydes with isatins
inferred← citeshttps://doi.org/10.1039/c5cc05617aopenalex-snapshot
Asymmetric vinylogous Michael reaction of cyclic enones with silyloxy furans
inferred← citeshttps://doi.org/10.1039/c6ra27026copenalex-snapshot
Alkaloids and polyketides from the South China Sea sponge Agelas aff. nemoechinata
inferred← citeshttps://doi.org/10.1039/c9ob01345hopenalex-snapshot
Diastereoselective multi-component tandem condensation: synthesis of 2-amino-4-(2-furanone)-4 H -chromene-3-carbonitriles
inferred← citeshttps://doi.org/10.1039/d4qo02195aopenalex-snapshot
Highly selective visible-light-induced cascade cyclization of vinyl sulfoxonium ylides with azides: a novel synthetic approach towards trisubstituted furans
inferred← citeshttps://doi.org/10.1080/10286020.2014.970535openalex-snapshot
Anticancer agents from marine sponges
inferred← citeshttps://doi.org/10.1080/10286020.2017.1385604openalex-snapshot
Furanone derivative and sesquiterpene from Antarctic marine-derived fungus Penicillium sp. S-1-18
inferred← citeshttps://doi.org/10.1080/14786419.2015.1104674openalex-snapshot
Two new polyketides from Nocardiopsis lucentensis DSM 44048
inferred← citeshttps://doi.org/10.1134/s1070428024110095openalex-snapshot
Synthesis of Polysubstituted Furans from α-Substituted 2-Enals
inferred← citeshttps://doi.org/10.1371/journal.pone.0174816openalex-snapshot
Sponge symbioses between Xestospongia deweerdtae and Plakortis spp. are not motivated by shared chemical defense against predators
inferred← citeshttps://doi.org/10.3390/antibiotics13121229openalex-snapshot
Bioactive Compounds Isolated from a Marine Sponge Selectively Inhibit Neisseria gonorrhoeae
inferred← citeshttps://doi.org/10.3390/md15050129openalex-snapshot
Chemistry and Selective Tumor Cell Growth Inhibitory Activity of Polyketides from the South China Sea Sponge Plakortis sp.
inferred← citeshttps://doi.org/10.3762/bjoc.20.88openalex-snapshot
A Diels–Alder probe for discovery of natural products containing furan moieties
inferred← citeshttps://doi.org/10.5772/intechopen.73529openalex-snapshot
Biological and Medicinal Importance of Sponge
inferred← citeshttps://doi.org/10.6023/a26050154openalex-snapshot
Advances in the Application of Mizoroki-Heck Reaction in Natural Product Synthesis ★
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