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Cytotoxic Pyrroloiminoquinones from Four New Species of South African Latrunculid Sponges
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4615-0747-5_78openalex-snapshot
Family Latrunculiidae Topsent, 1922
inferredcites →https://doi.org/10.1007/bf01958166openalex-snapshot
Purealidin A, a new cytotoxic bromotyrosine-derived alkaloid from the Okinawan marine spongePsammaplysilla purea
inferredcites →https://doi.org/10.1016/0040-4039(96)01560-2openalex-snapshot
New alkaloids from a South African latrunculid sponge
inferredcites →https://doi.org/10.1016/s0040-4020(01)86737-5openalex-snapshot
Cytotoxic pigments from new zealand sponges of the genus latrunculia : discorhabdins a, b and c
inferredcites →https://doi.org/10.1016/s0040-4020(01)96256-8openalex-snapshot
Makaluvamine G, a cytotoxic pigment from an an Indonesian Sponge Histodermella sp.
inferredcites →https://doi.org/10.1016/s0040-4039(01)80439-1openalex-snapshot
Batzellines A, B, and C. Novel pyrroloquinoline alkaloids from the sponge Batzella Sp.
inferredcites →https://doi.org/10.1021/ja00058a003openalex-snapshot
Novel cytotoxic topoisomerase II inhibiting pyrroloiminoquinones from Fijian sponges of the genus Zyzzya
inferredcites →https://doi.org/10.1021/jo00252a052openalex-snapshot
Discorhabdin D, an antitumor alkaloid from the sponges Latrunculia brevis and Prianos sp
inferredcites →https://doi.org/10.1021/jo00252a053openalex-snapshot
Titanium-induced reductive elimination of 2-yne-1,4-diols
inferredcites →https://doi.org/10.1021/jo00303a044openalex-snapshot
Transalkylation reactions of 4,4'-(1-methylethylidene)bisphenol with diphenyl ether
inferredcites →https://doi.org/10.1021/jo00376a096openalex-snapshot
Discorhabdin C, a highly cytotoxic pigment from a sponge of the genus Latrunculia
inferredcites →https://doi.org/10.1021/jo00376a097openalex-snapshot
Dramatic effects of oxygen substituents on 1,3-asymmetric induction in additions of allyltriphenylstannane to .beta.-alkoxy aldehydes: a chemical and spectroscopic investigation
inferredcites →https://doi.org/10.1021/np000220qopenalex-snapshot
Discorhabdin R: A New Antibacterial Pyrroloiminoquinone from Two Latrunculiid Marine Sponges, Latrunculia sp. and Negombata sp.
inferredcites →https://doi.org/10.1021/np030292sopenalex-snapshot
Discorhabdins S, T, and U, New Cytotoxic Pyrroloiminoquinones from a Deep-Water Caribbean Sponge of the Genus Batzella
inferredcites →https://doi.org/10.1021/np50126a008openalex-snapshot
Makaluvamines H-M and Damirone C from the Pohnpeian Sponge Zyzzya fuliginosa
inferredcites →https://doi.org/10.1021/np9607262openalex-snapshot
Makaluvamine N: A New Pyrroloiminoquinone from Zyzzya fuliginosa
inferredcites →https://doi.org/10.1021/np970580mopenalex-snapshot
Dilemmaones A−C, Unusual Indole Alkaloids from a Mixed Collection of South African Sponges
inferredcites →https://doi.org/10.1021/np980465ropenalex-snapshot
A New Discorhabdin from Two Sponge Genera
inferredcites →https://doi.org/10.1097/00001813-199609000-00007openalex-snapshot
Differences in the topoisomerase I cleavage complexes formed by camptothecin and wakayin, a DNA-intercalating marine natural product
inferredcites →https://doi.org/10.1097/00001813-199901000-00006openalex-snapshot
Makaluvamines vary in ability to induce dosedependent DNA cleavage via topoisomerase II interaction
inferredcites →https://doi.org/10.11646/zootaxa.371.1.1openalex-snapshot
South African Latrunculiidae (Porifera: Demospongiae: Poecilosclerida): descriptions of new species of Latrunculia du Bocage, Strongylodesma Lévi, and Tsitsikamma Samaai & Kelly
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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New Latrunculiidae (Demospongiae, Poecilosclerida) from the Agulhas ecoregion of temperate southern Africa
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Nanogram and Nanomolar Active Marine Antiplasmodial Antibiotics
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Porifera (Sponges)–2
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Porifera (Sponges)–5
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Structure and Biosynthesis of Halogenated Alkaloids
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Total Synthesis of (+)‐Discorhabdin V**
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Total Synthesis of (+)‐Discorhabdin V**
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Total Synthesis of Pyrroloiminoquinone Alkaloids
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Ten Years of Marine Natural Products Research at Rhodes University
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α‐Bromoacrylamido N‐Substituted Isatin Derivatives as Potent Inducers of Apoptosis in Human Myeloid Leukemia Cells
inferred← citeshttps://doi.org/10.1002/mbo3.417openalex-snapshot
Keeping it in the family: Coevolution of latrunculid sponges and their dominant bacterial symbionts
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Biosynthesis of Bioactive Metabolites of Marine Organisms
inferred← citeshttps://doi.org/10.1007/128_2011_134openalex-snapshot
Marine Pyrroloiminoquinone Alkaloids
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Marine Pyrroloiminoquinone Alkaloids, Makaluvamines and Discorhabdins, and Marine Pyrrole-Imidazole Alkaloids
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Targeting Conserved Pathways as a Strategy for Novel Drug Development: Disabling the Cellular Stress Response
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Natural Products from Sponges
inferred← citeshttps://doi.org/10.1007/978-981-97-1619-7_5openalex-snapshot
The Asymmetric Total Synthesis of Discorhabdin B, H, K, and Aleutianamine
inferred← citeshttps://doi.org/10.1007/s10126-012-9430-yopenalex-snapshot
Diversity of Bacterial Communities Associated with the Indian Ocean Sponge Tsitsikamma favus That Contains the Bioactive Pyrroloiminoquinones, Tsitsikammamine A and B
inferred← citeshttps://doi.org/10.1007/s10600-010-9553-1openalex-snapshot
STRONG ETHANOL SOLVATE OF DISCORHABDIN A ISOLATED FROM THE FAR-EAST SPONGE Latruculia oparinae
inferred← citeshttps://doi.org/10.1016/b978-0-12-398282-7.00001-1openalex-snapshot
Occurrence of Halogenated Alkaloids
inferred← citeshttps://doi.org/10.1016/bs.amb.2026.07.001openalex-snapshot
Marine benthic invertebrate biodiversity in South Africa: Advances and gaps in taxonomic and genetic knowledge
inferred← citeshttps://doi.org/10.1016/j.arabjc.2023.105011openalex-snapshot
Chemical diversity and biological activities of marine-derived sulphur containing alkaloids: A comprehensive update
inferred← citeshttps://doi.org/10.1016/j.bmcl.2005.09.063openalex-snapshot
Aza-analogues of the marine pyrroloquinoline alkaloids wakayin and tsitsikammamines: Synthesis and topoisomerase inhibition
inferred← citeshttps://doi.org/10.1016/j.bmcl.2007.02.048openalex-snapshot
Hybrid molecules containing benzo[4,5]imidazo[1,2-d][1,2,4]thiadiazole and α-bromoacryloyl moieties as potent apoptosis inducers on human myeloid leukaemia cells
inferred← citeshttps://doi.org/10.1016/j.bmcl.2009.02.038openalex-snapshot
Hybrid α-bromoacryloylamido chalcones. Design, synthesis and biological evaluation
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.11.036openalex-snapshot
Indoleamine 2,3-dioxygenase inhibitory activity of derivatives of marine alkaloid tsitsikammamine A
inferred← citeshttps://doi.org/10.1016/j.ejca.2006.05.019openalex-snapshot
Marine pharmacology in 2003–2004: Anti-tumour and cytotoxic compounds
inferred← citeshttps://doi.org/10.1016/j.ejmcr.2024.100158openalex-snapshot
Studies of chemical distribution and pharmacological activities of porifera-derived alkaloids: A review (2000–2023)
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.03.018openalex-snapshot
Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.11.031openalex-snapshot
Bioactive heterocycles containing endocyclic N-hydroxy groups
inferred← citeshttps://doi.org/10.1016/j.ejmech.2017.05.019openalex-snapshot
Discorhabdin alkaloids from Antarctic Latrunculia spp. sponges as a new class of cholinesterase inhibitors
inferred← citeshttps://doi.org/10.1016/j.ejmech.2024.116287openalex-snapshot
Biological properties of pyrroloquinoline and pyrroloisoquinoline derivatives
inferred← citeshttps://doi.org/10.1016/j.tet.2009.06.012openalex-snapshot
New natural products in the discorhabdin A- and B-series from New Zealand-sourced Latrunculia spp. sponges
inferred← citeshttps://doi.org/10.1016/j.tet.2013.03.052openalex-snapshot
Total synthesis of zyzzyanones A–D
inferred← citeshttps://doi.org/10.1016/j.tet.2017.06.057openalex-snapshot
Exploration of the influence of spiro-dienone moiety on biological activity of the cytotoxic marine alkaloid discorhabdin P
inferred← citeshttps://doi.org/10.1016/j.tetlet.2004.10.106openalex-snapshot
Novel pyrroloquinoline ribosides from the South African latrunculid sponge Strongylodesma aliwaliensis
inferred← citeshttps://doi.org/10.1016/j.tetlet.2008.12.078openalex-snapshot
Total synthesis of the marine pyrroloiminoquinone alkaloid tsitsikammamine A
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.04.021openalex-snapshot
A facile synthesis of bispyrroloquinone and bispyrroloiminoquinone ring system of marine alkaloids
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.06.014openalex-snapshot
Pyrroloquinoline derivatives from a Tongan specimen of the marine sponge Strongylodesma tongaensis
inferred← citeshttps://doi.org/10.1016/s1875-5364(15)30052-2openalex-snapshot
Recent advances in isolation, synthesis, and evaluation of bioactivities of bispyrroloquinone alkaloids of marine origin
inferred← citeshttps://doi.org/10.1017/s0025315409000101openalex-snapshot
A revision of the genus Strongylodesma Lévi (Porifera: Demospongiae: Latrunculiidae) with descriptions of four new species
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00023openalex-snapshot
Tridiscorhabdin and Didiscorhabdin, the First Discorhabdin Oligomers Linked with a Direct C–N Bridge from the Sponge Latrunculia biformis Collected from the Deep Sea in Antarctica
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.2c00987openalex-snapshot
A Quarter Century of Marine Biodiscovery in Algoa Bay, South Africa
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c01036openalex-snapshot
New Discorhabdin D Analogues from Latrunculia spp. Sponges
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b00846openalex-snapshot
Screening and Biological Effects of Marine Pyrroloiminoquinone Alkaloids: Potential Inhibitors of the HIF-1α/p300 Interaction
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02446openalex-snapshot
Entry into C1 Hydroxylated Discorhabdins
inferred← citeshttps://doi.org/10.1021/acselectrochem.5c00081openalex-snapshot
Nitro Substrates in Reductive Electrosynthesis: A Review
inferred← citeshttps://doi.org/10.1021/acsomega.5c11024openalex-snapshot
Fragment-Based Online OzESI-MS, NMR, and Computational DP4+/DFT Approaches to the Characterization of the Putative Biosynthetic Lipid Precursor of Atkamine from Alaskan Latrunculia Sponges
inferred← citeshttps://doi.org/10.1021/cr100435gopenalex-snapshot
Discorhabdins and Pyrroloiminoquinone-Related Alkaloids
inferred← citeshttps://doi.org/10.1021/jacs.3c06578openalex-snapshot
Unified Divergent Total Synthesis of Discorhabdin B, H, K, and Aleutianamine via the Late-Stage Oxidative N,S-Acetal Formation
inferred← citeshttps://doi.org/10.1021/jacs.4c11897openalex-snapshot
A Divergent Synthesis of Numerous Pyrroloiminoquinone Alkaloids Identifies Promising Antiprotozoal Agents
inferred← citeshttps://doi.org/10.1021/jm058012oopenalex-snapshot
Design, Synthesis, and Biological Evaluation of Hybrid Molecules Containing α-Methylene-γ-Butyrolactones and α-Bromoacryloyl Moieties
inferred← citeshttps://doi.org/10.1021/jm3002795openalex-snapshot
Antimalarial Activity of Pyrroloiminoquinones from the Australian Marine SpongeZyzzyasp.
inferred← citeshttps://doi.org/10.1021/jo801622nopenalex-snapshot
Enantiomeric Discorhabdin Alkaloids and Establishment of Their Absolute Configurations Using Theoretical Calculations of Electronic Circular Dichroism Spectra
inferred← citeshttps://doi.org/10.1021/np049589wopenalex-snapshot
Makaluvic Acids from the South African Latrunculid Sponge Strongylodesma aliwaliensis
inferred← citeshttps://doi.org/10.1021/np050154yopenalex-snapshot
Zyzzyanones B−D, Dipyrroloquinones from the Marine Sponge Zyzzya f uliginosa
inferred← citeshttps://doi.org/10.1021/np050333fopenalex-snapshot
Discorhabdin W, the First Dimeric Discorhabdin
inferred← citeshttps://doi.org/10.1021/np070179sopenalex-snapshot
Sanguinones A and B, Blue Pyrroloquinoline Alkaloids from the Fruiting Bodies of the Mushroom Mycena sanguinolenta
inferred← citeshttps://doi.org/10.1021/np100443copenalex-snapshot
Isolation and Characterization of Diastereomers of Discorhabdins H and K and Assignment of Absolute Configuration to Discorhabdins D, N, Q, S, T, and U
inferred← citeshttps://doi.org/10.1021/np900281ropenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/np9005629openalex-snapshot
Discorhabdins from the Korean Marine Sponge Sceptrella sp.
inferred← citeshttps://doi.org/10.1021/tx100282bopenalex-snapshot
Thiol-Activated DNA Damage by α-Bromo-2-cyclopentenone
inferred← citeshttps://doi.org/10.1039/b407299popenalex-snapshot
Pyrroloiminoquinone and related metabolites from marine sponges
inferred← citeshttps://doi.org/10.1039/b502162fopenalex-snapshot
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/b502166aopenalex-snapshot
Imidazole, oxazole and thiazole alkaloids
inferred← citeshttps://doi.org/10.1039/b516351jopenalex-snapshot
Simple indole alkaloids and those with a nonrearranged monoterpenoid unit
inferred← citeshttps://doi.org/10.1039/c2ob07090aopenalex-snapshot
Investigation of the electrophilic reactivity of the cytotoxic marine alkaloid discorhabdin B
inferred← citeshttps://doi.org/10.1039/c6ob01870jopenalex-snapshot
Short protecting-group-free synthesis of 5-acetylsulfanyl-histidines in water: novel precursors of 5-sulfanyl-histidine and its analogues
inferred← citeshttps://doi.org/10.1039/c9np00010kopenalex-snapshot
Natural cholinesterase inhibitors from marine organisms
inferred← citeshttps://doi.org/10.1039/d3qo01563gopenalex-snapshot
Enantioselective synthesis of pyrroloquinolines via a three-component Povarov reaction with aminoindoles
inferred← citeshttps://doi.org/10.1081/jlc-200052997openalex-snapshot
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inferred← citeshttps://doi.org/10.1128/mbio.01577-21openalex-snapshot
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inferred← citeshttps://doi.org/10.17159/sajs.2019/5534openalex-snapshot
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inferred← citeshttps://doi.org/10.2174/138955709787001640openalex-snapshot
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inferred← citeshttps://doi.org/10.3184/030823405775146915openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/biom11020258openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ma16031319openalex-snapshot
Green Synthesized sAuNPs as a Potential Delivery Platform for Cytotoxic Alkaloids
inferred← citeshttps://doi.org/10.3390/md13031105openalex-snapshot
Anticancer Properties of Lamellarins
inferred← citeshttps://doi.org/10.3390/md15020047openalex-snapshot
Antibacterial Activities of Bacteria Isolated from the Marine Sponges Isodictya compressa and Higginsia bidentifera Collected from Algoa Bay, South Africa
inferred← citeshttps://doi.org/10.3390/md16070241openalex-snapshot
Preclinical Evaluation of Discorhabdins in Antiangiogenic and Antitumor Models
inferred← citeshttps://doi.org/10.3390/md16080268openalex-snapshot
Targeted Isolation of Tsitsikammamines from the Antarctic Deep-Sea Sponge Latrunculia biformis by Molecular Networking and Anticancer Activity
inferred← citeshttps://doi.org/10.3390/md17010060openalex-snapshot
Molecular Networking Reveals Two Distinct Chemotypes in Pyrroloiminoquinone-Producing Tsitsikamma favus Sponges
inferred← citeshttps://doi.org/10.3390/md17080439openalex-snapshot
New Discorhabdin Alkaloids from the Antarctic Deep-Sea Sponge Latrunculia biformis
inferred← citeshttps://doi.org/10.3390/md18020107openalex-snapshot
New Discorhabdin B Dimers with Anticancer Activity from the Antarctic Deep-Sea Sponge Latrunculia biformis
inferred← citeshttps://doi.org/10.3390/md19010027openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md19020068openalex-snapshot
Unlocking the Diversity of Pyrroloiminoquinones Produced by Latrunculid Sponge Species
inferred← citeshttps://doi.org/10.3390/md20010075openalex-snapshot
Marine Organisms as Alkaloid Biosynthesizers of Potential Anti-Alzheimer Agents
inferred← citeshttps://doi.org/10.3390/md21090474openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md8041394openalex-snapshot
Synthesis of the Marine Pyrroloiminoquinone Alkaloids, Discorhabdins
inferred← citeshttps://doi.org/10.3390/molecules24010188openalex-snapshot
Discorhabdin N, a South African Natural Compound, for Hsp72 and Hsc70 Allosteric Modulation: Combined Study of Molecular Modeling and Dynamic Residue Network Analysis
inferred← citeshttps://doi.org/10.3390/molecules27248724openalex-snapshot
Current Perspectives on Pyrroloiminoquinones: Distribution, Biosynthesis and Drug Discovery Potential
inferred← citeshttps://doi.org/10.3390/toxins16120531openalex-snapshot
Image Analysis and Untargeted Metabolomics Reveal Potential Phytotoxins from Fusarium venenatum Against Major Parasitic Weed Phelipanche ramosa (L.) Pomel
inferred← citeshttps://doi.org/10.3897/zookeys.874.32268openalex-snapshot
New species in the sponge genus Tsitsikamma (Poecilosclerida, Latrunculiidae) from South Africa
inferred← citeshttps://doi.org/10.4236/cc.2018.63005openalex-snapshot
Theoretical Study by Density Functional Theory Method (DFT) of Stability, Tautomerism, Reactivity and Prediction of Acidity of Quinolein-4-One Derivatives
inferred← citeshttps://doi.org/10.52547/ismj.24.4.341openalex-snapshot
Sea God- Sponges: Toxins and Secondary Metabolites
inferred← citeshttps://doi.org/10.6023/a26050154openalex-snapshot
Advances in the Application of Mizoroki-Heck Reaction in Natural Product Synthesis ★
inferred← citeshttps://doi.org/10.70675/94aeb578z2c7bz424dzb9caza4ffeedbe0dcopenalex-snapshot
Synthèse totale d'un alcaloïde marin : Wakayine et étude d'analogues ayant une activité immunothérapeutique potentielle
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