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Scytophycins, cytotoxic and antimycotic agents from the cyanophyte Scytonema pseudohofmanni

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Action of tolytoxin on cell morphology, cytoskeletal organization, and actin polymerization
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Stereochemistry of ulapualides, a new family of tris-oxazole-containing macrolide ionophores from marine nudibranchs. A molecular mechanics study
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Two classes of metabolites fromTheonella swinhoei are localized in distinct populations of bacterial symbionts
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Effects of rhizopodin and latrunculin B on the morphology and on the actin cytoskeleton of mammalian cells
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Analysis and Detection of Scytophycin Variants by HPLC-ESI-MS
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Stereoselective VO(acac)2 catalyzed epoxidation of acyclic homoallylic diols. Complementary preparation of C2-syn-3,4-epoxy alcohols
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Lewis-acid catalyzed formation of dihydropyrans
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Synthesis of cis-2,6-tetrahydropyran-4-one via diastereoselectively intramolecular cyclization of β-hydroxy allyl ketone
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Gold(I) catalysed cycloisomerisation of β-hydroxy propargylic esters to dihydropyrans/2H-pyrans via allene intermediates
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PdII-Catalyzed stereospecific formation of tetrahydro- and 3,6-dihydro[2H]pyran rings: 1,3-chirality transfer by intramolecular oxypalladation reaction
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A simple and efficient synthesis of goniothalesdiol A
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First stereoselective total synthesis of phomonol via oxa-Michael approach
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Catalytic asymmetric synthesis of key intermediate for scytophycin C
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Toward the total synthesis of scytophycins: Synthesis of the C7–C21 fragments of scytophycins A, B, and C
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Three new potent cytotoxic macrolides closely related to sphinxolide from the new caledonian sponge neosiphonia superstes
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Sphinxolides E-G and reidispongiolide C: four new cytotoxic macrolides from the new caledonian lithistida sponges N. superstes and R. coeruleaXXX
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Non-Toxic Peptides from Toxic Cyanobacteria, Oscillatoria agardhii
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Antitumor macrodiolides isolated from a marine sponge sp.: Structure revision of misakinolide A
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Studies in marine macrolide synthesis: A stereocontrolled synthesis of a C17-C32 subunit of scytophycin C.
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Studies in marine macrolide synthesis: Asymmetric synthesis of C1-C15/C16 subunits of swinholide A and scytophycin C.
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Towards the synthesis of swinholide A and scytophycin C. A highly stereocontrolled synthesis of (−)-pre-swinholide A
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Mirabazoles, minor tantazole-related cytotoxins from the terrestrial blue-green alga scytonema mirabile
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)78876-9openalex-snapshot
A stereocontrolled synthesis of a C19-C32 / C17-C30 Segment for swinholide A and misakinolide A, Cytotoxic dimeric macrolides from theonella swinhoei.
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Synthetic studies towards halichondramides, and related novel tris-oxazole containing macrolides from marine organisms. A concise route to the keto-triol formyl enamine moiety.
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Goniodomin a, a novel polyether macrolide from the dinoflagellate goniodoma pseudogoniaulax
inferred← citeshttps://doi.org/10.1016/s0040-4039(00)93962-5openalex-snapshot
The isolation of a monomeric carboxylic acid of swinholide a from the indo-pacific sponge, theonella swinhoei
inferred← citeshttps://doi.org/10.1016/s0040-4039(02)01705-7openalex-snapshot
A stereoconvergent synthesis of the C(19)C(31) fragment of scytophycin C
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Synthesis of the C(19)C(32) fragment of scytophycin C via stereospecific methylation of γ,δ-epoxy acrylates with trimethylaluminum
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Studies directed toward the total synthesis of scytophycin C: Synthesis of the C(1)C(18) fragment of scytophycin C
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Total synthesis of ulapualide A, a novel tris-oxazole containing macrolide from the marine nudibranch Hexabranchus sanguineus
inferred← citeshttps://doi.org/10.1016/s0040-4039(99)00868-0openalex-snapshot
Studies of fragment assembly aldol reactions of chiral aldehydes and chiral methyl ketones: stereoselective synthesis of the C(13)–C(25) segment of scytophycin C
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Biogenetic Diversity of Cyanobacterial Metabolites
inferred← citeshttps://doi.org/10.1016/s0065-2725(08)60070-7openalex-snapshot
Aromatic Biheterocycles: Syntheses, Structures, and Properties
inferred← citeshttps://doi.org/10.1016/s0099-9598(01)57003-0openalex-snapshot
Nitrogen-containing metabolites from marine cyanobacteria
inferred← citeshttps://doi.org/10.1016/s0099-9598(08)60127-3openalex-snapshot
Chapter 6 Oxazole Alkaloids
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Chapter 15 Application of Biotechnology to Coastal Lagoons
inferred← citeshttps://doi.org/10.1016/s0944-5013(99)80043-3openalex-snapshot
Inhibitory metabolites production by the cyanobacterium Fischerella muscicola
inferred← citeshttps://doi.org/10.1016/s0957-4166(03)00372-0openalex-snapshot
Stereochemical assignment of the C23–C35 portion of sphinxolide/reidispongiolide class of natural products by asymmetric synthesis
inferred← citeshttps://doi.org/10.1016/s1572-5995(02)80027-8openalex-snapshot
The chemistry of lithistid sponge: A spectacular source of new metabolites
inferred← citeshttps://doi.org/10.1016/s1572-5995(96)80015-9openalex-snapshot
Bioactive marine macrolides
inferred← citeshttps://doi.org/10.1021/acs.biochem.6c00103openalex-snapshot
Structure, Biosynthesis, and Bioactivity of Nostolysamides
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00896openalex-snapshot
Ulapualides C–E Isolated from a Hawaiian Hexabranchus sanguineus Egg Mass
inferred← citeshttps://doi.org/10.1021/acs.joc.6b01154openalex-snapshot
Stereochemistry of PdII-Catalyzed THF Ring Formation of ε-Hydroxy Allylic Alcohols and Synthesis of 2,3,5-Trisubstituted and 2,3,4,5-Tetrasubstituted Tetrahydrofurans
inferred← citeshttps://doi.org/10.1021/acs.joc.8b00028openalex-snapshot
Samholides, Swinholide-Related Metabolites from a Marine Cyanobacterium cf. Phormidium sp.
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03840openalex-snapshot
Structure–Activity Relationship Studies on Scytophycin B, a Spiro-Epoxide-Containing Cytotoxic Macrolide
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02056openalex-snapshot
Formal Synthesis of Premisakinolide A and C(19)–C(32) of Swinholide A via Site-Selective C–H Allylation and Crotylation of Unprotected Diols
inferred← citeshttps://doi.org/10.1021/ja204570wopenalex-snapshot
Direct Generation of Acyclic Polypropionate Stereopolyads via Double Diastereo- and Enantioselective Iridium-Catalyzed Crotylation of 1,3-Diols: Beyond Stepwise Carbonyl Addition in Polyketide Construction
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Enantioselective Synthesis of (Z)- and (E)-2-Methyl-1,5-anti-Pentenediols via an Allene Hydroboration–Double-Allylboration Reaction Sequence
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Enantioselective Alcohol C–H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis
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A Convolutional Neural Network-Based Approach for the Rapid Annotation of Molecularly Diverse Natural Products
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Palladium-Catalyzed Stereospecific Synthesis of 2,6-Disubstituted Tetrahydropyrans: 1,3-Chirality Transfer by an Intramolecular Oxypalladation Reaction
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Highly Stereocontrolled Synthesis of trans -2,6-Disubstituted-5-methyl-3,6-dihydropyrans: Stereoselective Synthesis of the Bicyclic Core of Penostatin B
inferred← citeshttps://doi.org/10.1021/jo800704dopenalex-snapshot
Electrophile-Induced Ether Transfer: Stereoselective Synthesis of 2,6-Disubstituted-3,4-Dihydropyrans
inferred← citeshttps://doi.org/10.1021/jo8023494openalex-snapshot
Biomimetic Transannular Oxa-Conjugate Addition Approach to the 2,6-Disubstituted Dihydropyran of Laulimalide Yields an Unprecedented Transannular Oxetane
inferred← citeshttps://doi.org/10.1021/jo962189wopenalex-snapshot
Total Synthesis of Scytophycin C
inferred← citeshttps://doi.org/10.1021/np049912vopenalex-snapshot
Research Achievement AwardD. John Faulkner
inferred← citeshttps://doi.org/10.1021/np100045fopenalex-snapshot
Richard E. Moore (1933−2007)
inferred← citeshttps://doi.org/10.1021/ol035227oopenalex-snapshot
Total Synthesis of Scytophycin C. 1. Stereoselective Syntheses of the C(1)−C(18) Segment and the C(19)−C(31) Segment
inferred← citeshttps://doi.org/10.1021/ol0352299openalex-snapshot
Total Synthesis of Scytophycin C. 2. Coupling Reaction of the C(1)−C(18) Segment and the C(19)−C(31) Segment, a Key Macrolactonization, and the Crucial Terminal Amidation Reaction
inferred← citeshttps://doi.org/10.1021/ol050188xopenalex-snapshot
Isolation of Swinholide A and Related Glycosylated Derivatives from Two Field Collections of Marine Cyanobacteria
inferred← citeshttps://doi.org/10.1021/ol050864vopenalex-snapshot
Stereoselective Synthesis of Premisakinolide A, the Monomeric Counterpart of the Marine 40-Membered Dimeric Macrolide Misakinolide A
inferred← citeshttps://doi.org/10.1021/ol070506nopenalex-snapshot
Highly Stereoselective Prins Cyclization of (Z)- and (E)-γ-Brominated Homoallylic Alcohols to 2,4,5,6-Tetrasubstituted Tetrahydropyrans
inferred← citeshttps://doi.org/10.1038/nchembio.1870openalex-snapshot
Metabolic and evolutionary origin of actin-binding polyketides from diverse organisms
inferred← citeshttps://doi.org/10.1039/a805873copenalex-snapshot
Biosynthesis of marine natural products: microorganisms and macroalgae
inferred← citeshttps://doi.org/10.1039/b000750lopenalex-snapshot
Towards a total synthesis of ulapualide A. Concise synthetic routes to the tris-oxazole ring system and tris-oxazole macrolide core in ulapualides, kabiramides, halichondramides, mycalolides and halishigamides
inferred← citeshttps://doi.org/10.1039/b000751jopenalex-snapshot
A total synthesis of the unique tris-oxazole macrolide ulapualide A produced by the marine nudibranch Hexabranchus sanguineus
inferred← citeshttps://doi.org/10.1039/b003939jopenalex-snapshot
Biosynthesis and attachment of novel bacterial polyketide synthase starter units
inferred← citeshttps://doi.org/10.1039/b301384gopenalex-snapshot
Merging the potential of microbial genetics with biological and chemical diversity: an even brighter future for marine natural product drug discovery
inferred← citeshttps://doi.org/10.1039/b517149kopenalex-snapshot
Possibility of a non-amino acid pathway in the biosynthesis of marine-derived oxazoles
inferred← citeshttps://doi.org/10.1039/b703499gopenalex-snapshot
Metabolites from symbiotic bacteria
inferred← citeshttps://doi.org/10.1039/b800263kopenalex-snapshot
Aplyronine A, a potent antitumour macrolide of marine origin, and the congeners aplyronines B–H: chemistry and biology
inferred← citeshttps://doi.org/10.1039/b801036fopenalex-snapshot
Total synthesis of (−)-ulapualide A, a novel tris-oxazole macrolide from marine nudibranchs, based on some biosynthesis speculation
inferred← citeshttps://doi.org/10.1039/c5np00125kopenalex-snapshot
Biosynthesis of polyketides by trans-AT polyketide synthases
inferred← citeshttps://doi.org/10.1039/c6sc05246kopenalex-snapshot
Rhodium( i )-catalyzed stereoselective [4+2] cycloaddition of oxetanols with alkynes through C(sp 3 )–C(sp 3 ) bond cleavage
inferred← citeshttps://doi.org/10.1039/c7np00010copenalex-snapshot
Antibiotics from Gram-negative bacteria: a comprehensive overview and selected biosynthetic highlights
inferred← citeshttps://doi.org/10.1039/c7qo00664kopenalex-snapshot
Total synthesis of natural products via iridium catalysis
inferred← citeshttps://doi.org/10.1039/c9ob02689dopenalex-snapshot
CuBr 2 -catalyzed diastereoselective allylation: total synthesis of decytospolides A and B and their C6-epimers
inferred← citeshttps://doi.org/10.1039/np9931000593openalex-snapshot
Biosynthesis of fatty acid and polyketide metabolites
inferred← citeshttps://doi.org/10.1039/p19930001629openalex-snapshot
Naturally occurring linear fused thiazoline-thiazole containing metabolites: total synthesis of (–)-didehydromirabazole A, a cytotoxic alkaloid from blue–green algae
inferred← citeshttps://doi.org/10.1046/j.1440-1835.1998.00117.xopenalex-snapshot
Control of the plant pathogenic fungus Macrophomina phaseolina in mung bean by a microalgal extract
inferred← citeshttps://doi.org/10.1055/s-0035-1546055openalex-snapshot
Anti-infective Natural Products from Cyanobacteria
inferred← citeshttps://doi.org/10.1073/pnas.0401548101openalex-snapshot
Synthesis of antimicrofilament marine macrolides: Synthesis and configurational assignment of a C 5 –C 16 degradation fragment of reidispongiolide A
inferred← citeshttps://doi.org/10.1073/pnas.1131855100openalex-snapshot
Seaweed resistance to microbial attack: A targeted chemical defense against marine fungi
inferred← citeshttps://doi.org/10.1073/pnas.2233339100openalex-snapshot
Biomolecular mimicry in the actin cytoskeleton: Mechanisms underlying the cytotoxicity of kabiramide C and related macrolides
inferred← citeshttps://doi.org/10.1080/08927010600967261openalex-snapshot
Antifouling potential of cyanobacteria: a mini-review
inferred← citeshttps://doi.org/10.1080/10826079308020925openalex-snapshot
Determination of Scytophycins in Cyanophyte Cultures by High Performance Liquid Chromatography
inferred← citeshttps://doi.org/10.1111/j.0022-3646.1991.00530.xopenalex-snapshot
ANTINEOPLASTIC ACTIVITY OF CULTURED BLUE‐GREEN ALGAE (CYANOPHYTA)1
inferred← citeshttps://doi.org/10.1111/j.0022-3646.1997.00054.xopenalex-snapshot
FUNGAL CELLWALL POLYSACCHARIDES ELICIT AN ANTIFUNGAL SECONDARY METABOLITE (PHYTOALEXIN) IN THE CYANOBACTERIUM SCYTONEMA OCELUTUM2
inferred← citeshttps://doi.org/10.1111/j.1440-1681.1996.tb01770.xopenalex-snapshot
A FAMILY OF NOVEL ACTIN‐INHIBITING MARINE TOXINS
inferred← citeshttps://doi.org/10.1111/j.1440-1835.1998.tb00263.xopenalex-snapshot
Control of the plant pathogenic fungus Macrophomina phaseolina in mung bean by a microalgal extract
inferred← citeshttps://doi.org/10.1111/j.1749-6632.1988.tb40395.xopenalex-snapshot
Antifungal Substances from Marine Invertebrates
inferred← citeshttps://doi.org/10.11606/d.11.2022.tde-11082022-145740openalex-snapshot
Terpenoma de cianobactérias isoladas de lagoas salino-alcalinas do Pantanal
inferred← citeshttps://doi.org/10.1201/9781420027976.ch1.19openalex-snapshot
Food Applications of Algae
inferred← citeshttps://doi.org/10.1201/b13868-15openalex-snapshot
Microalgae as Sources of Biomaterials and Pharmaceuticals
inferred← citeshttps://doi.org/10.1201/b13868-35openalex-snapshot
Anticancer Compounds from Marine Microorganisms
inferred← citeshttps://doi.org/10.1242/jcs.112.9.1291openalex-snapshot
Dynein is required for spindle assembly in cytoplasmic extracts of Spisula solidissima oocytes
inferred← citeshttps://doi.org/10.1242/jcs.112.9.1325openalex-snapshot
New actin mutants allow further characterization of the nucleotide binding cleft and drug binding sites
inferred← citeshttps://doi.org/10.1248/yakushi.23-00161-2openalex-snapshot
Up to Date of Cyanobacterial Natural Products
inferred← citeshttps://doi.org/10.1517/13543784.12.8.1367openalex-snapshot
Marine-derived anticancer agents in clinical trials
inferred← citeshttps://doi.org/10.1533/9781845698164.1.24openalex-snapshot
Structural Analysis of Cyanobacterial Toxins
inferred← citeshttps://doi.org/10.18006/2021.9(5).543.571openalex-snapshot
PHARMACEUTICAL POTENTIAL OF LABORATORY GROWN CULTURES OF BLUE-GREEN ALGAE: A COMPREHENSIVE REVIEW AND FUTURE POSSIBILITIES
inferred← citeshttps://doi.org/10.2174/1389201016666150826121124openalex-snapshot
Cyanobacteria as a Source for Novel Anti-Leukemic Compounds
inferred← citeshttps://doi.org/10.2478/abmj-2023-0012openalex-snapshot
A Mini Review on Biotechnological Potentials of Bioactive Compounds and Bioproducts Isolated from Cyanobacteria
inferred← citeshttps://doi.org/10.3389/fmicb.2017.00515openalex-snapshot
Uncovering Potential Applications of Cyanobacteria and Algal Metabolites in Biology, Agriculture and Medicine: Current Status and Future Prospects
inferred← citeshttps://doi.org/10.3390/ijms23052623openalex-snapshot
Microalgal Biorefinery Concepts’ Developments for Biofuel and Bioproducts: Current Perspective and Bottlenecks
inferred← citeshttps://doi.org/10.3390/ijms24076195openalex-snapshot
Epoxide-Based Synthetic Approaches toward Polypropionates and Related Bioactive Natural Products
inferred← citeshttps://doi.org/10.3390/md10040812openalex-snapshot
Marine Bioactives: Pharmacological Properties and Potential Applications against Inflammatory Diseases
inferred← citeshttps://doi.org/10.3390/md13042124openalex-snapshot
Antifungal Compounds from Cyanobacteria
inferred← citeshttps://doi.org/10.3390/md15050126openalex-snapshot
A Review Study on Macrolides Isolated from Cyanobacteria
inferred← citeshttps://doi.org/10.3390/md17040241openalex-snapshot
Marine Macrolides with Antibacterial and/or Antifungal Activity
inferred← citeshttps://doi.org/10.3390/md21060359openalex-snapshot
Cyanobacteria: A Promising Source of Antifungal Metabolites
inferred← citeshttps://doi.org/10.3390/molecules28207127openalex-snapshot
A Review of the Antimicrobial Properties of Cyanobacterial Natural Products
inferred← citeshttps://doi.org/10.3390/org6030029openalex-snapshot
Complementary Synthesis of Anti- and Syn-Hydroxymethyl 1,3-Diols via Regioselective Ring Opening of TIPS-Protected 2,3-Epoxy Alcohols: Toward Polypropionate Fragments
inferred← citeshttps://doi.org/10.3923/jbs.2007.904.910openalex-snapshot
Antifungal and Antibacterial Activity of the Microalgae Collected from Paddy Fields of Iran: Characterization of Antimicrobial Activity of Chroococcus dispersus
inferred← citeshttps://doi.org/10.4014/jmb.2001.01015openalex-snapshot
Effect of the MicroalgaChlorella fuscaCHK0059 on Strawberry PGPR and Biological Control of Fusarium Wilt Disease in Non-Pesticide Hydroponic Strawberry Cultivation
inferred← citeshttps://doi.org/10.5433/2316-5200.2013v2n1p49openalex-snapshot
Cianobactérias: uma revisão sobre potencial nutricional e alguns aspectos biotecnológicos
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