On the public citation graph
The chemistry and biology of cytochalasans
0 signed · 539 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-0029(19991001)47:1<18::aid-jemt3>3.0.co;2-eopenalex-snapshot
New anti-actin drugs in the study of the organization and function of the actin cytoskeleton
inferredcites →https://doi.org/10.1002/1439-7633(20020703)3:7<619::aid-cbic619>3.0.co;2-9openalex-snapshot
Big Effects from Small Changes: Possible Ways to Explore Nature's Chemical Diversity
inferredcites →https://doi.org/10.1002/anie.197303701openalex-snapshot
The Cytochalasans: A New Class of Biologically Active Microbial Metabolites
inferredcites →https://doi.org/10.1002/anie.200200534openalex-snapshot
Chemistry and Biology of Biosynthetic Diels–Alder Reactions
inferredcites →https://doi.org/10.1002/anie.200806121openalex-snapshot
The Biosynthetic Logic of Polyketide Diversity
inferredcites →https://doi.org/10.1002/cbic.200400138openalex-snapshot
Fusarin C Biosynthesis in Fusarium moniliforme and Fusarium venenatum
inferredcites →https://doi.org/10.1002/cbic.200600398openalex-snapshot
Biosynthesis of the 2‐Pyridone Tenellin in the Insect Pathogenic Fungus Beauveria bassiana
inferredcites →https://doi.org/10.1002/cbic.200700390openalex-snapshot
Authentic Heterologous Expression of the Tenellin Iterative Polyketide Synthase Nonribosomal Peptide Synthetase Requires Coexpression with an Enoyl Reductase
inferredcites →https://doi.org/10.1002/ejoc.200801085openalex-snapshot
Spicochalasin A and New Aspochalasins from the Marine‐Derived Fungus Spicaria elegans
inferredcites →https://doi.org/10.1002/hlca.19700530728openalex-snapshot
Zur Biogenese des Antibioticums Phomin. 1. Teil: Die Grundbausteine
inferredcites →https://doi.org/10.1002/hlca.19730560312openalex-snapshot
Desoxaphomin, das erste [13]Cytochalasan, ein möglicher biogenetischer Vorläufer der 24‐Oxa‐[14]cytochalasane
inferredcites →https://doi.org/10.1002/hlca.19730560722openalex-snapshot
Proxiphomin und Protophomin, zwei neue Cytochalasane
inferredcites →https://doi.org/10.1002/hlca.19740570629openalex-snapshot
Biosynthese der Cytochalasane. Teil II Die Grundbausteine von Cytochalasin D
inferredcites →https://doi.org/10.1002/hlca.19740570630openalex-snapshot
Biosynthesis of the Cytochalasans. Part III. 13C‐NMR. of cytochalasin B (phomin) and cytochalasin D. Incorporation of [1‐13C]‐ and [2‐13C]‐sodium acetate
inferredcites →https://doi.org/10.1002/hlca.19750580704openalex-snapshot
Biosynthesis of Cytochalasans. Part 4. The mode of incorporation of common naturally‐occurring carboxylic acids into cytochalasin D
inferredcites →https://doi.org/10.1002/hlca.19750580830openalex-snapshot
Biosynthesis of cytochalasans. Part 5. The Incorporation of Deoxaphomin into Cytochalasin B (Phomin)
inferredcites →https://doi.org/10.1002/hlca.19760590221openalex-snapshot
Biosynthesis of Cytochalasans. Part 6. The Mode of Incorporation of Phenylalanine into Cytochalasin D
inferredcites →https://doi.org/10.1002/hlca.19800630622openalex-snapshot
Differential Hydrogen Exchange During Biosynthesis of Cytochalasins B and D
inferredcites →https://doi.org/10.1002/hlca.19810640711openalex-snapshot
Biosynthesis of the Cytochalasans. Biosynthetic studies on chaetoglobosin A and 19‐O‐acetylchaetoglobosin A
inferredcites →https://doi.org/10.1002/hlca.19830660206openalex-snapshot
Approaches to the Synthesis of Cytochalasans. Part 4. Improved Synthesis of the Tetrahydroisoindoline Subunits Related to the Cytochalasins and Aspochalasins
inferredcites →https://doi.org/10.1002/hlca.200800455openalex-snapshot
Bioactive Cytochalasins from Aspergillus flavipes, an Endophytic Fungus Associated with the Mangrove Plant Acanthus ilicifolius
inferredcites →https://doi.org/10.1006/excr.1997.3798openalex-snapshot
Effects of Multidrug Resistance-Related ATP-Binding-Cassette Transporter Proteins on the Cytoskeletal Activity of Cytochalasins
inferredcites →https://doi.org/10.1007/bf00594629openalex-snapshot
Cytochalasin stops tip growth in plants
inferredcites →https://doi.org/10.1007/bf01138601openalex-snapshot
Penicillium aurantiogriseum Dierckx produces chaetoglobosin A toxic to embryonic chickens
inferredcites →https://doi.org/10.1007/bf02026363openalex-snapshot
Cytotoxicity of new cytochalasans fromChaetomium globosum
inferredcites →https://doi.org/10.1007/s00018-006-6157-9openalex-snapshot
Actin-targeting natural products: structures, properties and mechanisms of action
inferredcites →https://doi.org/10.1007/s00436-004-1106-8openalex-snapshot
Different effects of cytochalasins on the growth and differentiation of Entamoeba invadens
inferredcites →https://doi.org/10.1016/0003-2697(79)90178-7openalex-snapshot
Interaction between rabbit muscle actin and several chaetoglobosins or cytochalasins
inferredcites →https://doi.org/10.1016/0005-2760(91)90219-8openalex-snapshot
Inhibition of phosphatidylcholine and phosphatidylethanolamine biosynthesis by cytochalasin B in cultured glioma cells: Potential regulation of biosynthesis by Ca2+-dependent mechanisms
inferredcites →https://doi.org/10.1016/0006-291x(71)90617-6openalex-snapshot
Cytochalasin B inhibits thyroid secretion
inferredcites →https://doi.org/10.1016/0040-4020(95)00139-yopenalex-snapshot
Phomopsichalasin, a novel antimicrobial agent from an endophytic Phomopsis sp.
inferredcites →https://doi.org/10.1016/0040-4039(91)80032-2openalex-snapshot
New plausible precursors of chaetoglobosin a accumulated by treatment of chaetomium subaffine with cytochrome P-450 inhibitors
inferredcites →https://doi.org/10.1016/0040-4039(96)00778-2openalex-snapshot
New cytochalasins: Synthetic studies of a novel HIV-1 protease inhibitor
inferredcites →https://doi.org/10.1016/0092-8674(80)90619-4openalex-snapshot
Mechanism of action of cytochalasin B on actin
inferredcites →https://doi.org/10.1016/0304-4165(78)90027-2openalex-snapshot
Mechanism of corticotropin action in rat adrenal cells I. The effects of inhibitors of protein synthesis and of microfilament formation on corticosterone synthesis
inferredcites →https://doi.org/10.1016/j.bmc.2007.11.042openalex-snapshot
Alachalasins A–G, new cytochalasins from the fungus Stachybotrys charatum
inferredcites →https://doi.org/10.1016/j.bmc.2007.11.084openalex-snapshot
Corrigendum to “Alachalasins A–G, new cytochalasins from the fungus Stachybotrys charatum” [Bioorg. Med. Chem. 16 (2008) 2627–2634]
inferredcites →https://doi.org/10.1016/j.bmcl.2009.04.073openalex-snapshot
Functional expression of the Aspergillus flavus PKS–NRPS hybrid CpaA involved in the biosynthesis of cyclopiazonic acid
inferredcites →https://doi.org/10.1016/j.femsle.2005.07.038openalex-snapshot
Diversity of type I polyketide synthase genes in the wood-decay fungusXylariasp. BCC 1067
inferredcites →https://doi.org/10.1016/j.fgb.2003.10.010openalex-snapshot
A mutation in the Neurospora crassa actin gene results in multiple defects in tip growth and branching
inferredcites →https://doi.org/10.1016/j.fgb.2008.09.006openalex-snapshot
Identification of a novel polyketide synthase–nonribosomal peptide synthetase (PKS–NRPS) gene required for the biosynthesis of cyclopiazonic acid in Aspergillus oryzae
inferredcites →https://doi.org/10.1016/j.jbiotec.2006.03.046openalex-snapshot
Advances in cloning, functional analysis and heterologous expression of fungal polyketide synthase genes
inferredcites →https://doi.org/10.1016/j.jmb.2008.09.082openalex-snapshot
Crystal Structures of Monomeric Actin Bound to Cytochalasin D
inferredcites →https://doi.org/10.1016/j.pbi.2009.06.004openalex-snapshot
Fungal phytotoxins as mediators of virulence
inferredcites →https://doi.org/10.1016/j.phytochem.2007.11.003openalex-snapshot
Nonenolides and cytochalasins with phytotoxic activity against Cirsium arvense and Sonchus arvensis: A structure–activity relationships study
inferredcites →https://doi.org/10.1016/s0009-2797(02)00164-3openalex-snapshot
Short-chain dehydrogenases/reductases (SDR): the 2002 update
inferredcites →https://doi.org/10.1016/s0021-9258(17)38480-6openalex-snapshot
The involvement of cellular ATP in receptor-mediated internalization of epidermal growth factor and hormone-induced internalization of beta-adrenergic receptors.
inferredcites →https://doi.org/10.1016/s0021-9258(18)52391-7openalex-snapshot
Actin: protein structure and filament dynamics.
inferredcites →https://doi.org/10.1016/s0021-9258(18)67925-6openalex-snapshot
The Biosynthesis of Sphingosine
inferredcites →https://doi.org/10.1016/s0021-9258(18)71199-xopenalex-snapshot
THE BIOSYNTHESIS OF SPHINGOSINE
inferredcites →https://doi.org/10.1016/s0021-9258(19)70620-6openalex-snapshot
Intracellular movement of cholesterol in rat adrenal cells. Kinetics and effects of inhibitors.
inferredcites →https://doi.org/10.1016/s0021-9258(19)86105-7openalex-snapshot
Cytochalasins block actin filament elongation by binding to high affinity sites associated with F-actin.
inferredcites →https://doi.org/10.1016/s0021-9258(19)86107-0openalex-snapshot
The effects of cytochalasins on actin polymerization and actin ATPase provide insights into the mechanism of polymerization.
inferredcites →https://doi.org/10.1016/s0022-1910(97)00066-8openalex-snapshot
Effects of the entomopathogenic fungus Metarhizium anisopliae and its secondary metabolites on morphology and cytoskeleton of plasmatocytes isolated from the greater wax moth, Galleria mellonella
inferredcites →https://doi.org/10.1016/s0022-3565(24)39088-3openalex-snapshot
Cytochalasin E, an Epoxide ContainingAspergillus-Derived Fungal Metabolite, Inhibits Angiogenesis and Tumor Growth
inferredcites →https://doi.org/10.1016/s0040-4020(01)00153-3openalex-snapshot
Cytotoxic cytochalasans from a Penicillium species separated from a marine alga
inferredcites →https://doi.org/10.1016/s0167-4838(98)00040-5openalex-snapshot
Enzymatic activity and partial purification of solanapyrone synthase: first enzyme catalyzing Diels–Alder reaction
inferredcites →https://doi.org/10.1016/s1074-5521(00)00011-9openalex-snapshot
The biosynthetic gene cluster for the antitumor drug bleomycin from Streptomyces verticillus ATCC15003 supporting functional interactions between nonribosomal peptide synthetases and a polyketide synthase
inferredcites →https://doi.org/10.1016/s1074-5521(00)00075-2openalex-snapshot
The biosynthetic gene cluster for the microtubule-stabilizing agents epothilones A and B from Sorangium cellulosum So ce90
inferredcites →https://doi.org/10.1016/s1074-5521(02)00284-3openalex-snapshot
Small Molecules, Big Impact
inferredcites →https://doi.org/10.1021/ar00008a002openalex-snapshot
Cytochalasan synthesis: macrocycle formation via intramolecular Diels-Alder reactions
inferredcites →https://doi.org/10.1021/bi00221a034openalex-snapshot
Effects of cytochalasin, phalloidin and pH on the elongation of actin filaments
inferredcites →https://doi.org/10.1021/bi00545a011openalex-snapshot
Structure of cytochalasins and cytochalasin B binding sites in human erythrocyte membranes
inferredcites →https://doi.org/10.1021/bi00747a036openalex-snapshot
Inhibition of glucose transport in the human erythrocyte by cytochalasin B
inferredcites →https://doi.org/10.1021/cr050001fopenalex-snapshot
Chemistry and Biology of Mycotoxins and Related Fungal Metabolites
inferredcites →https://doi.org/10.1021/cr0503097openalex-snapshot
Assembly-Line Enzymology for Polyketide and Nonribosomal Peptide Antibiotics: Logic, Machinery, and Mechanisms
inferredcites →https://doi.org/10.1021/ja00167a036openalex-snapshot
Synthesis of cytochalasins: the route to sulfur-bridged [11]cytochalasans
inferredcites →https://doi.org/10.1021/ja00167a037openalex-snapshot
The total syntheses of dl-zygosporin E and dl-C18-desmethylcytochalasin D
inferredcites →https://doi.org/10.1021/ja00203a042openalex-snapshot
Palladium-catalyzed synthesis of macrocycles. A total synthesis of (-)-aspochalasin B
inferredcites →https://doi.org/10.1021/ja003216+openalex-snapshot
Lovastatin Nonaketide Synthase Catalyzes an Intramolecular Diels−Alder Reaction of a Substrate Analogue
inferredcites →https://doi.org/10.1021/ja00328a053openalex-snapshot
Total synthesis of carbocyclic cytochalasans
inferredcites →https://doi.org/10.1021/ja00354a072openalex-snapshot
A simplified total synthesis of cytochalasins via an intramolecular Diels-Alder reaction
inferredcites →https://doi.org/10.1021/ja00492a082openalex-snapshot
Total synthesis of cytochalasin B
inferredcites →https://doi.org/10.1021/ja072884topenalex-snapshot
Molecular Basis of Cytochalasan Biosynthesis in Fungi: Gene Cluster Analysis and Evidence for the Involvement of a PKS-NRPS Hybrid Synthase by RNA Silencing
inferredcites →https://doi.org/10.1021/ja803078zopenalex-snapshot
Thioesterase-Like Role for Fungal PKS-NRPS Hybrid Reductive Domains
inferredcites →https://doi.org/10.1021/ja8091054openalex-snapshot
A PLP-Dependent Polyketide Chain Releasing Mechanism in the Biosynthesis of Mycotoxin Fumonisins inFusarium verticillioides
inferredcites →https://doi.org/10.1021/jf035406kopenalex-snapshot
Penicilliumexpansum: Consistent Production of Patulin, Chaetoglobosins, and Other Secondary Metabolites in Culture and Their Natural Occurrence in Fruit Products
inferredcites →https://doi.org/10.1021/jf061405ropenalex-snapshot
Production of Mutagenic Metabolites by Metarhizium anisopliae
inferredcites →https://doi.org/10.1021/jf8004178openalex-snapshot
Production of Phytotoxins by Phoma exigua var. exigua, a Potential Mycoherbicide against Perennial Thistles
inferredcites →https://doi.org/10.1021/jm00348a011openalex-snapshot
Structure-activity correlations of cytochalasins. Novel halogenated and related cytochalasin C and D derivatives
inferredcites →https://doi.org/10.1021/jo01333a052openalex-snapshot
An approach to enolonium equivalents. Application to a total synthesis of (.+-.)-pyrenophorin
inferredcites →https://doi.org/10.1021/jo962321sopenalex-snapshot
Phomacins: Three Novel Antitumor Cytochalasan Constituents Produced by a Phoma sp.
inferredcites →https://doi.org/10.1021/np030252oopenalex-snapshot
Cytochalasins Z4, Z5, and Z6, Three New 24-Oxa[14]cytochalasans Produced by Phoma exigua var. heteromorpha
inferredcites →https://doi.org/10.1021/np030353mopenalex-snapshot
Aspochalasins I, J, and K: Three New Cytotoxic Cytochalasans of Aspergillus flavipes from the Rhizosphere of Ericameria laricifolia of the Sonoran Desert
inferredcites →https://doi.org/10.1021/np030460gopenalex-snapshot
Chaetoglobosins Q, R, and T, Three Further New Metabolites from Chaetomium globosum
inferredcites →https://doi.org/10.1021/np0498206openalex-snapshot
Botryane Metabolites from the Fungus Geniculosporium sp. Isolated from the Marine Red Alga Polysiphonia
inferredcites →https://doi.org/10.1021/np049974lopenalex-snapshot
Isolation and Structure of Antagonists of Chemokine Receptor (CCR5)
inferredcites →https://doi.org/10.1021/np050515+openalex-snapshot
Chaetoglobosin U, a Cytochalasan Alkaloid from Endophytic Chaetomium globosum IFB-E019
inferredcites →https://doi.org/10.1021/np0600649openalex-snapshot
Pimarane Diterpene and Cytochalasin Derivatives from the Endophytic Fungus Eutypella scoparia PSU-D44
inferredcites →https://doi.org/10.1021/np070539bopenalex-snapshot
Novel Open-Chain Cytochalsins from the Marine-Derived Fungus Spicaria elegans
inferredcites →https://doi.org/10.1021/np50095a013openalex-snapshot
Microbial Transformation of L-696, 474, a Novel Cytochalasin as an Inhibitor of HIV-1 Protease
inferredcites →https://doi.org/10.1021/np9802670openalex-snapshot
Geniculol, a New Biologically Active Diterpene from the Endophytic Fungus Geniculosporium sp.
inferredcites →https://doi.org/10.1021/np990331topenalex-snapshot
Zygosporin D and Two New Cytochalasins Produced by the Fungus Metarrhizium anisopliae
inferredcites →https://doi.org/10.1023/a:1011921031564openalex-snapshot
Antiproliferative and Cytotoxic Effects of Geldanamycin, Cytochalasin E, Suramin and Thiacetazone in Human Prostate Xenograft Tumor Histocultures
inferredcites →https://doi.org/10.1038/213261a0openalex-snapshot
Effects of Cytochalasins on Mammalian Cells
inferredcites →https://doi.org/10.1038/2161134a0openalex-snapshot
Action of Cytochalasin B on Cultured Human Lymphocytes
inferredcites →https://doi.org/10.1038/234215a0openalex-snapshot
Complete Fusion induced by Krypton Ions: Indications for Synthesis of Superheavy Nuclei
inferredcites →https://doi.org/10.1038/ja.2005.34openalex-snapshot
A Novel Aspochalasin with HIV-1 Integrase Inhibitory Activity from Aspergillus flavipes
inferredcites →https://doi.org/10.1038/nchembio869openalex-snapshot
Genomics-driven discovery of PKS-NRPS hybrid metabolites from Aspergillus nidulans
inferredcites →https://doi.org/10.1038/newbio234215a0openalex-snapshot
Cytochalasin B and Release of Growth Hormone
inferredcites →https://doi.org/10.1039/a906412eopenalex-snapshot
Total synthesis of cytochalasin D: total synthesis and full structural assignment of cytochalasin O
inferredcites →https://doi.org/10.1039/a909079gopenalex-snapshot
Polyketide biosynthesis: a millennium review
inferredcites →https://doi.org/10.1039/b100918oopenalex-snapshot
Endophytes: a rich source of functional metabolites (1987 to 2000)
inferredcites →https://doi.org/10.1039/b305068hopenalex-snapshot
Enzymatic catalysis of the Diels–Alder reaction in the biosynthesis of natural products
inferredcites →https://doi.org/10.1039/b413523gopenalex-snapshot
Equisetin biosynthesis in Fusarium heterosporum
inferredcites →https://doi.org/10.1039/b514050copenalex-snapshot
Polyketide synthases and nonribosomal peptide synthetases: the emerging view from bacterial genomics
inferredcites →https://doi.org/10.1039/b704420hopenalex-snapshot
Polyketides, proteins and genes in fungi: programmed nano-machines begin to reveal their secrets
inferredcites →https://doi.org/10.1039/b713084hopenalex-snapshot
Determination of mycotoxins in human foods
inferredcites →https://doi.org/10.1039/b814552kopenalex-snapshot
Intramolecular cyclizations of polyketide biosynthesis: mining for a “Diels–Alderase”?
inferredcites →https://doi.org/10.1039/b821578bopenalex-snapshot
Triggering cryptic natural product biosynthesis in microorganisms
inferredcites →https://doi.org/10.1039/b904543kopenalex-snapshot
Structural insights into nonribosomal peptide enzymatic assembly lines
inferredcites →https://doi.org/10.1039/c19670000026openalex-snapshot
The cytochalasins, a new class of biologically active mould metabolites
inferredcites →https://doi.org/10.1039/c39860000727openalex-snapshot
Cytochalasan synthesis: total synthesis of cytochalasin H
inferredcites →https://doi.org/10.1039/c39860001447openalex-snapshot
Cytochalasan synthesis: total synthesis of cytochalasin G
inferredcites →https://doi.org/10.1039/c39900000464openalex-snapshot
Cytochalasan synthesis: total synthesis of cytochalasin D
inferredcites →https://doi.org/10.1039/p19730001146openalex-snapshot
Nomenclature of a class of biologically active mould metabolites: the cytochalasins, phomins, and zygosporins
inferredcites →https://doi.org/10.1039/p19890000507openalex-snapshot
Cytochalasan synthesis: total synthesis of cytochalasin H
inferredcites →https://doi.org/10.1039/p19920002955openalex-snapshot
Biosynthetic study of chaetoglobosin A: origins of the oxygen and hydrogen atoms, and indirect evidence for biological Diels–Alder reaction
inferredcites →https://doi.org/10.1039/p19960000239openalex-snapshot
Penochalasins, a novel class of cytotoxic cytochalasans from a Penicillium species separated from a marine alga: structure determination and solution conformation
inferredcites →https://doi.org/10.1073/pnas.0402111101openalex-snapshot
An enantioselective, modular, and general route to the cytochalasins: Synthesis of L-696,474 and cytochalasin B
inferredcites →https://doi.org/10.1073/pnas.69.2.442openalex-snapshot
Cytochalasin B, Its Interaction with Actin and Actomyosin from Muscle
inferredcites →https://doi.org/10.1073/pnas.69.6.1430openalex-snapshot
Cytochalasin B: Inhibition of Glucose and Glucosamine Transport
inferredcites →https://doi.org/10.1073/pnas.72.3.869openalex-snapshot
Cell cycle studies of mononucleate and cytochalasin-B--nduced binucleate fibroblasts.
inferredcites →https://doi.org/10.1073/pnas.79.12.3759openalex-snapshot
Inhibition of glucose transport in human erythrocytes by cytochalasins: A model based on diffraction studies.
inferredcites →https://doi.org/10.1083/jcb.102.1.282openalex-snapshot
Cytochalasin B slows but does not prevent monomer addition at the barbed end of the actin filament.
inferredcites →https://doi.org/10.1083/jcb.105.4.1473openalex-snapshot
Effects of cytochalasin and phalloidin on actin.
inferredcites →https://doi.org/10.1083/jcb.116.4.933openalex-snapshot
Direct proof that the primary site of action of cytochalasin on cell motility processes is actin.
inferredcites →https://doi.org/10.1083/jcb.88.3.487openalex-snapshot
Mechanism of action of cytochalasin: evidence that it binds to actin filament ends.
inferredcites →https://doi.org/10.1093/pcp/pcm030openalex-snapshot
Wide-Ranging Effects of Eight Cytochalasins and Latrunculin A and B on Intracellular Motility and Actin Filament Reorganization in Characean Internodal Cells
inferredcites →https://doi.org/10.1099/00221287-71-2-343openalex-snapshot
Antimicrobial Properties of Cytochalasins and Their Alteration of Fungal Morphology
inferredcites →https://doi.org/10.1099/00221287-87-1-177openalex-snapshot
Cytochalasins A and B from Strains of Phoma exigua var. exigua and Formation of Cytochalasin B in Potato Gangrene
inferredcites →https://doi.org/10.1126/science.171.3967.135openalex-snapshot
Microfilaments in Cellular and Developmental Processes
inferredcites →https://doi.org/10.1126/science.284.5418.1368openalex-snapshot
Modulation of Polyketide Synthase Activity by Accessory Proteins During Lovastatin Biosynthesis
inferredcites →https://doi.org/10.1128/jb.137.2.925-932.1979openalex-snapshot
Physiological responses of bacteria to cytochalasin A: effects on growth, transport, and enzyme induction
inferredcites →https://doi.org/10.1248/cpb.21.2268openalex-snapshot
Structure-Activity Relationships among Zygosporin Derivatives
inferredcites →https://doi.org/10.1248/cpb.30.1609openalex-snapshot
Chaetoglobosins, cytotoxic 10-(indol-3-yl)-(13)cytochalasans from Chaetomium spp. I. Production, isolation and some cytological effects of chaetoglobosins A-J.
inferredcites →https://doi.org/10.1248/cpb.30.1618openalex-snapshot
Chaetoglobosins, cytotoxic 10-(indo-3-yl)-(13)cytochalasans from Chaetomium spp. II. Structures of chaetoglobosins A, B, and D.
inferredcites →https://doi.org/10.1248/cpb.30.1629openalex-snapshot
Chaetoglobosins, cytotoxic 10-(indol-3-yl)-(13)cytochalasans from Chaetomium spp. III. Structures of chaetoglobosins C, E, F, G, and J.
inferredcites →https://doi.org/10.1248/cpb.38.971openalex-snapshot
The effects of new cytochalasins from Phomopsis sp. and the derivatives on cellular structure and actin polymerization.
inferredcites →https://doi.org/10.1271/bbb1961.51.2625openalex-snapshot
Pyrichalasin H, a new phytotoxic metabolite belonging to the cytochalasans from Pyricularia grisea (Cooke) Saccardo.
inferredcites →https://doi.org/10.2174/156800906776842948openalex-snapshot
Specialisation of the Tropomyosin Composition of Actin Filaments Provides New Potential Targets for Chemotherapy
inferredcites →https://doi.org/10.7164/antibiotics.21.523openalex-snapshot
ZYGOSPORIN A, A NEW ANTIBIOTIC FROM ZYGOSPORIUM MASONII
inferredcites →https://doi.org/10.7164/antibiotics.22.170openalex-snapshot
THE IDENTITY OF ZYGOSPORIN A AND CYTOCHALASIN D
inferredcites →https://doi.org/10.7164/antibiotics.35.1345openalex-snapshot
Structural features of cytochalasins responsible for gram-positive bacterial inhibitions.
inferredcites →https://doi.org/10.7164/antibiotics.45.671openalex-snapshot
L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease. I. The producing organism and its fermentation.
inferredcites →https://doi.org/10.7164/antibiotics.45.679openalex-snapshot
L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease. II. Isolation and structure.
inferredcites →https://doi.org/10.7164/antibiotics.45.686openalex-snapshot
L-696,474, a novel cytochalasin as an inhibitor of HIV-1 protease. III. Biological activity.
inferredcites →https://doi.org/10.7164/antibiotics.57.715openalex-snapshot
Aspochalamins A-D and Aspochalasin Z Produced by the Endosymbiotic Fungus Aspergillus niveus LU 9575: II. Structure Elucidation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.113009zenodo-depositor-declared
Bioactive cytochalasans from the fungus Arthrinium arundinis DJ-13
inferred← citeshttps://doi.org/10.3897/mycokeys.107.127749zenodo-depositor-declared
Novel discoveries of Xylariomycetidae (Ascomycota) taxa from peat swamp forests and other terrestrial habitats in Thailand
inferred← citeshttps://doi.org/10.1002/9781119949138.ch15openalex-snapshot
Fungal Secondary Metabolites: Ancient Toxins and Novel Effectors in Plant–Microbe Interactions
inferred← citeshttps://doi.org/10.1002/ange.201506264openalex-snapshot
Asperchalasine A, a Cytochalasan Dimer with an Unprecedented Decacyclic Ring System, from Aspergillus flavipes
inferred← citeshttps://doi.org/10.1002/ange.201511315openalex-snapshot
Epicochalasines A and B: Two Bioactive Merocytochalasans Bearing Caged Epicoccine Dimer Units from Aspergillus flavipes
inferred← citeshttps://doi.org/10.1002/ange.201602439openalex-snapshot
Total Syntheses of Periconiasins A–E
inferred← citeshttps://doi.org/10.1002/ange.201701125openalex-snapshot
Asperflavipine A: A Cytochalasan Heterotetramer Uniquely Defined by a Highly Complex Tetradecacyclic Ring System from Aspergillus flavipes QCS12
inferred← citeshttps://doi.org/10.1002/ange.201808249openalex-snapshot
Total Syntheses of Asperchalasines A–E
inferred← citeshttps://doi.org/10.1002/ange.201808481openalex-snapshot
Total Synthesis of Asperchalasines A, D, E, and H
inferred← citeshttps://doi.org/10.1002/ange.201809703openalex-snapshot
Biomimetic Synthesis of (+)‐Aspergillin PZ
inferred← citeshttps://doi.org/10.1002/ange.202102831openalex-snapshot
Bioinspired Network Analysis Enabled Divergent Syntheses and Structure Revision of Pentacyclic Cytochalasans
inferred← citeshttps://doi.org/10.1002/ange.202524740openalex-snapshot
Bioinspired Total Synthesis of Curtachalasin B and Biosynthetically Related Cytochalasans
inferred← citeshttps://doi.org/10.1002/anie.201506264openalex-snapshot
Asperchalasine A, a Cytochalasan Dimer with an Unprecedented Decacyclic Ring System, from Aspergillus flavipes
inferred← citeshttps://doi.org/10.1002/anie.201511315openalex-snapshot
Epicochalasines A and B: Two Bioactive Merocytochalasans Bearing Caged Epicoccine Dimer Units from Aspergillus flavipes
inferred← citeshttps://doi.org/10.1002/anie.201602439openalex-snapshot
Total Syntheses of Periconiasins A–E
inferred← citeshttps://doi.org/10.1002/anie.201701125openalex-snapshot
Asperflavipine A: A Cytochalasan Heterotetramer Uniquely Defined by a Highly Complex Tetradecacyclic Ring System from Aspergillus flavipes QCS12
inferred← citeshttps://doi.org/10.1002/anie.201808249openalex-snapshot
Total Syntheses of Asperchalasines A–E
inferred← citeshttps://doi.org/10.1002/anie.201808481openalex-snapshot
Total Synthesis of Asperchalasines A, D, E, and H
inferred← citeshttps://doi.org/10.1002/anie.201809703openalex-snapshot
Biomimetic Synthesis of (+)‐Aspergillin PZ
inferred← citeshttps://doi.org/10.1002/anie.202102831openalex-snapshot
Bioinspired Network Analysis Enabled Divergent Syntheses and Structure Revision of Pentacyclic Cytochalasans
inferred← citeshttps://doi.org/10.1002/anie.202524740openalex-snapshot
Bioinspired Total Synthesis of Curtachalasin B and Biosynthetically Related Cytochalasans
inferred← citeshttps://doi.org/10.1002/cbdv.201300218openalex-snapshot
Bioactive Tyrosine‐Derived Cytochalasins from Fungus Eutypella sp. D‐1
inferred← citeshttps://doi.org/10.1002/cbdv.202000957openalex-snapshot
Westalsan: A New Acetylcholine Esterase Inhibitor from the Endophytic FungusWesterdykella nigra
inferred← citeshttps://doi.org/10.1002/cbdv.202200550openalex-snapshot
New Cytochalasin Derivatives from Deep‐Sea Cold Seep‐Derived Endozoic Fungus Curvularia verruculosa CS‐129
inferred← citeshttps://doi.org/10.1002/cbdv.202400567openalex-snapshot
Diaporchalasins A–E, New Cytochalasins from the Endophytic Fungus Diaporthe sp. BMX12 Isolated from Aquilaria sinensis
inferred← citeshttps://doi.org/10.1002/cbdv.202503213openalex-snapshot
Cytochalasinols A and B, Two New Cytochalasins From the Fungus Xylaria necrophora SZSS1‐2‐2
inferred← citeshttps://doi.org/10.1002/cbdv.71594openalex-snapshot
Amiaspochalasins I and J, Undescribed Aspochalasins with Antibacterial Activities From Aspergillus micronesiensis
inferred← citeshttps://doi.org/10.1002/cbic.201100798openalex-snapshot
Establishing a New Methodology for Genome Mining and Biosynthesis of Polyketides and Peptides through Yeast Molecular Genetics
inferred← citeshttps://doi.org/10.1002/cbic.201200449openalex-snapshot
Evolutionary Imprint of Catalytic Domains in Fungal PKS–NRPS Hybrids
inferred← citeshttps://doi.org/10.1002/cbic.201200624openalex-snapshot
Molecular Diversity Sculpted by Fungal PKS–NRPS Hybrids
inferred← citeshttps://doi.org/10.1002/cbic.202500794openalex-snapshot
Exploring the Substitution of the C 21‐OAc Moiety in [11]Cytochalasans: Synthesis and Evaluation of Fluorophore Conjugates
inferred← citeshttps://doi.org/10.1002/chem.201501252openalex-snapshot
Directed Hydrogenations and an Ireland–Claisen Rearrangement Linked to Evans–Tishchenko Chemistry: The Highly Efficient Total Synthesis of the Marine Cyclodepsipeptide Doliculide
inferred← citeshttps://doi.org/10.1002/chem.201603734openalex-snapshot
First Total Synthesis, Structure Revision, and Natural History of the Smallest Cytochalasin: (+)‐Periconiasin G
inferred← citeshttps://doi.org/10.1002/chem.201804023openalex-snapshot
Multifaceted Study on a Cytochalasin Scaffold: Lessons on Reactivity, Multidentate Catalysis, and Anticancer Properties
inferred← citeshttps://doi.org/10.1002/chem.202002241openalex-snapshot
Diversely Functionalised Cytochalasins through Mutasynthesis and Semi‐Synthesis
inferred← citeshttps://doi.org/10.1002/chem.202004444openalex-snapshot
Chemical and Genetic Studies on the Formation of Pyrrolones During the Biosynthesis of Cytochalasans
inferred← citeshttps://doi.org/10.1002/chem.202302590openalex-snapshot
Reductive Release from a Hybrid PKS‐NRPS during the Biosynthesis of Pyrichalasin H
inferred← citeshttps://doi.org/10.1002/chin.201037271openalex-snapshot
ChemInform Abstract: The Chemistry and Biology of Cytochalasans
inferred← citeshttps://doi.org/10.1002/chir.22068openalex-snapshot
Chaetoglobosin Vb from Endophytic Chaetomium Globosum: Absolute Configuration of Chaetoglobosins
inferred← citeshttps://doi.org/10.1002/cjoc.202200215openalex-snapshot
Ergochaeglobosins A—E, Unprecedented Heterodimers of Cytochalasan and Ergosterol fromChaeglobosin globosum P2 ‐2‐2
inferred← citeshttps://doi.org/10.1002/cjoc.202200744openalex-snapshot
Talachalasins A—C, Undescribed Cytochalasans with a 16β‐Methyl or 2‐Oxabicyclo [3.3.1]nonan‐3‐one unit from the Deep‐Sea‐Derived Fungus Talaromyces muroii sp. SCSIO 40439
inferred← citeshttps://doi.org/10.1002/cm.21624openalex-snapshot
Actomyosin‐dependent invasion of endothelial sprouts in collagen
inferred← citeshttps://doi.org/10.1002/ejoc.201403678openalex-snapshot
Armochaetoglobins K–R, Anti‐HIV Pyrrole‐Based Cytochalasans from Chaetomium globosum TW1‐1
inferred← citeshttps://doi.org/10.1002/hlca.201100051openalex-snapshot
New Cytochalasins from the Marine‐Derived Fungus Xylaria sp. SCSIO 156
inferred← citeshttps://doi.org/10.1002/jms.3922openalex-snapshot
Biosynthesis and mass spectral fragmentation pathways of 13C and 15N labeled cytochalasin D produced by Xylaria arbuscula
inferred← citeshttps://doi.org/10.1002/med.21348openalex-snapshot
Toward a Cancer Drug of Fungal Origin
inferred← citeshttps://doi.org/10.1002/rcm.6329openalex-snapshot
Electrospray ionization tandem mass spectrometry of chaetoglobosins
inferred← citeshttps://doi.org/10.1002/rcm.8306openalex-snapshot
Diagnostic fragmentation filtering for the discovery of new chaetoglobosins and cytochalasins
inferred← citeshttps://doi.org/10.1002/smll.202410861openalex-snapshot
NQO1‐Responsive Prodrug for in Cellulo Release of Cytochalasin B as Cancer Cell‐Targeted Migrastatic
inferred← citeshttps://doi.org/10.1007/978-1-0716-1661-1_9openalex-snapshot
Influencing the Actin Dynamics in Plant Cells by Jasplakinolide, Chondramides, Phalloidin, Cytochalasins, and Latrunculins
inferred← citeshttps://doi.org/10.1007/978-1-4939-1191-2_12openalex-snapshot
Lovastatin, Compactin, and Related Anticholesterolemic Agents
inferred← citeshttps://doi.org/10.1007/978-1-4939-3124-8_13openalex-snapshot
Actin-Dynamics in Plant Cells: The Function of Actin-Perturbing Substances: Jasplakinolide, Chondramides, Phalloidin, Cytochalasins, and Latrunculins
inferred← citeshttps://doi.org/10.1007/978-3-030-21110-3_13openalex-snapshot
Frontier in Antifungal Treatments Against Major Human Fungal Opportunistic Pathogen Candida Species and Medically Important Fungi
inferred← citeshttps://doi.org/10.1007/978-3-030-30746-2_9openalex-snapshot
Fungal Polyketides: Chemical Diversity and Their Cytotoxic Effects
inferred← citeshttps://doi.org/10.1007/978-3-030-31612-9_10openalex-snapshot
The Use of Chaetomium Taxa as Biocontrol Agents
inferred← citeshttps://doi.org/10.1007/978-3-030-59444-2_1openalex-snapshot
Progress in the Chemistry of Cytochalasans
inferred← citeshttps://doi.org/10.1007/978-3-030-67561-5_7openalex-snapshot
Exploring Fungal Biodiversity of Genus Epicoccum and Their Biotechnological Potential
inferred← citeshttps://doi.org/10.1007/978-3-319-19456-1_22-1openalex-snapshot
Preclinical and Clinical Perspective on Fungal Metabolites and Their Analogs as Anticancer Agents – From Bench to Bedside
inferred← citeshttps://doi.org/10.1007/978-3-319-25001-4_22openalex-snapshot
Preclinical and Clinical Perspective on Fungal Metabolites and Their Analogs as Anticancer Agents – From Bench to Bedside
inferred← citeshttps://doi.org/10.1007/978-3-319-71740-1_12openalex-snapshot
Polyketide Synthase–Nonribosomal Peptide Synthetase Hybrid Enzymes of Fungi
inferred← citeshttps://doi.org/10.1007/978-3-319-89833-9_16openalex-snapshot
Bioactive Compounds from Tree Endophytes
inferred← citeshttps://doi.org/10.1007/978-94-007-1599-8_17openalex-snapshot
Antimicrobial Compounds from Tree Endophytes
inferred← citeshttps://doi.org/10.1007/978-981-13-5862-3_2openalex-snapshot
Secondary Metabolites of Metarhizium spp. and Verticillium spp. and Their Agricultural Applications
inferred← citeshttps://doi.org/10.1007/s00253-021-11630-2openalex-snapshot
Cytochalasans and azaphilones: suitable chemotaxonomic markers for the Chaetomium species
inferred← citeshttps://doi.org/10.1007/s00253-023-12501-8openalex-snapshot
Enhanced production of aspochalasin D through genetic engineering of Aspergillus flavipes
inferred← citeshttps://doi.org/10.1007/s10544-017-0222-zopenalex-snapshot
Development of a shear stress-free microfluidic gradient generator capable of quantitatively analyzing single-cell morphology
inferred← citeshttps://doi.org/10.1007/s10600-021-03374-2openalex-snapshot
Chaetoglobosins in Endophytic Chaetomium sp. from Astragalus membranaceus
inferred← citeshttps://doi.org/10.1007/s10637-014-0202-6openalex-snapshot
Chemotherapy in vivo against M109 murine lung carcinoma with cytochalasin B by localized, systemic, and liposomal administration
inferred← citeshttps://doi.org/10.1007/s10637-014-0203-5openalex-snapshot
Chemotherapy with cytochalasin congeners in vitro and in vivo against murine models
inferred← citeshttps://doi.org/10.1007/s11274-017-2274-xopenalex-snapshot
Identification and characterization of the major antifungal substance against Fusarium Sporotrichioides from Chaetomium globosum
inferred← citeshttps://doi.org/10.1007/s11427-012-4409-5openalex-snapshot
A PKS gene, pks-1, is involved in chaetoglobosin biosynthesis, pigmentation and sporulation in Chaetomium globosum
inferred← citeshttps://doi.org/10.1007/s11557-021-01704-wopenalex-snapshot
Biologically active secondary metabolites and biotechnological applications of species of the family Chaetomiaceae (Sordariales): an updated review from 2016 to 2021
inferred← citeshttps://doi.org/10.1007/s11557-021-01739-zopenalex-snapshot
Phylogenetic analysis of Engleromyces sinensis and identification of cytochalasin D from culture
inferred← citeshttps://doi.org/10.1007/s11557-022-01816-xopenalex-snapshot
Studies on the secondary metabolism of Rosellinia and Dematophora strains (Xylariaceae) from Iran
inferred← citeshttps://doi.org/10.1007/s11596-024-2922-yopenalex-snapshot
Michael Acceptor Pyrrolidone Derivatives and Their Activity against Diffuse Large B-cell Lymphoma
inferred← citeshttps://doi.org/10.1007/s12088-013-0362-7openalex-snapshot
Antifungal Metabolites Produced by Chaetomium globosum No.04, an Endophytic Fungus Isolated from Ginkgo biloba
inferred← citeshttps://doi.org/10.1007/s12325-017-0513-zopenalex-snapshot
Targeting Schlemm’s Canal in the Medical Therapy of Glaucoma: Current and Future Considerations
inferred← citeshttps://doi.org/10.1007/s12550-012-0144-9openalex-snapshot
Chaetoglobosins and azaphilones produced by Canadian strains of Chaetomium globosum isolated from the indoor environment
inferred← citeshttps://doi.org/10.1007/s13213-017-1256-4openalex-snapshot
Isolation and characterization of trichalasin-producing endophytic fungus from Taxus baccata
inferred← citeshttps://doi.org/10.1007/s13659-020-00279-5openalex-snapshot
Cytochalasins from Xylaria sp. CFL5, an Endophytic Fungus of Cephalotaxus fortunei
inferred← citeshttps://doi.org/10.1007/s13659-025-00507-wopenalex-snapshot
Xylariaides A and B, novel cytochalasans with a unique 5/6/5/3 ring system from a soil fungus Xylaria sp. Y01
inferred← citeshttps://doi.org/10.1007/s13659-025-00572-1openalex-snapshot
Harziachalasins A–G, polycyclic-fused cytochalasins from the endophytic fungus Trichoderma harzianum MLJ-4 with HIV latency reversal activity
inferred← citeshttps://doi.org/10.1007/s13659-026-00651-xopenalex-snapshot
Cytochalasins are a fascinating class of natural compounds: advances in the chemistry, biological activities, mode of action, and structure-activity relationships of novel cytochalasins isolated in the last decade are described
inferred← citeshttps://doi.org/10.1007/s43393-025-00330-xopenalex-snapshot
Recent advances in the biosynthesis of cytochalasans: a review
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14637-2openalex-snapshot
Oxidative Modification Enzymes in Polyketide Biosynthetic Pathways
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14677-3openalex-snapshot
Fungal Polyketide-Nonribosomal Peptide Synthetases and Their Associated Natural Products
inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.21118-7openalex-snapshot
Antitumor and Immunomodulatory Compounds from Fungi
inferred← citeshttps://doi.org/10.1016/b978-0-12-811790-3.00003-1openalex-snapshot
Bioinspired Adventures in the Total Synthesis of Mixed Polyketide–Nonribosomal Peptide Natural Products
inferred← citeshttps://doi.org/10.1016/b978-0-12-821005-5.00001-6openalex-snapshot
Fungal metabolites: A recent trend and its potential biotechnological applications
inferred← citeshttps://doi.org/10.1016/b978-0-12-821006-2.00008-xopenalex-snapshot
A promising source of anticancer drug from fungal secondary metabolite
inferred← citeshttps://doi.org/10.1016/b978-0-323-95241-5.00019-8openalex-snapshot
Fungal metabolites as anticancer agent and their agricultural applications
inferred← citeshttps://doi.org/10.1016/b978-0-444-53836-9.00025-6openalex-snapshot
Diversity and Ecological Significance of Fungal Endophyte Natural Products
inferred← citeshttps://doi.org/10.1016/b978-0-444-63473-3.00009-5openalex-snapshot
Bioactive Natural Products from Marine-Derived Fungi
inferred← citeshttps://doi.org/10.1016/bs.adgen.2016.01.005openalex-snapshot
Molecular Genetics of Secondary Chemistry in Metarhizium Fungi
inferred← citeshttps://doi.org/10.1016/j.bbamem.2015.11.022openalex-snapshot
Small molecule pinocytosis and clathrin-dependent endocytosis at the intestinal brush border: Two separate pathways into the enterocyte
inferred← citeshttps://doi.org/10.1016/j.bbcan.2014.09.007openalex-snapshot
Exploiting the cytoskeletal filaments of neoplastic cells to potentiate a novel therapeutic approach
inferred← citeshttps://doi.org/10.1016/j.biocontrol.2012.10.005openalex-snapshot
Efficacy assessment of antifungal metabolites from Chaetomium globosum No.05, a new biocontrol agent, against Setosphaeria turcica
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104317openalex-snapshot
Cytochalasins from an endophytic fungus Phoma multirostrata XJ-2-1 with cell cycle arrest and TRAIL-resistance-overcoming activities
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109304openalex-snapshot
Genome analysis-led discovery of antimicrobial and herbicidal cytochalasans from the cold-seep-sourced endozoic Curvularia verruculosa CS-129
inferred← citeshttps://doi.org/10.1016/j.bjp.2015.08.003openalex-snapshot
Antibacterial, antifungal and cytotoxic activities exhibited by endophytic fungi from the Brazilian marine red alga Bostrychia tenella (Ceramiales)
inferred← citeshttps://doi.org/10.1016/j.bmcl.2012.03.058openalex-snapshot
Cytotoxic cytochalasins from the endozoic fungus Phoma sp. of the giant jellyfish Nemopilema nomurai
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.03.080openalex-snapshot
Cytochalasin derivatives from a jellyfish-derived fungus Phoma sp.
inferred← citeshttps://doi.org/10.1016/j.bse.2011.06.019openalex-snapshot
Antifungal metabolites from Chaetomium globosum, an endophytic fungus in Ginkgo biloba
inferred← citeshttps://doi.org/10.1016/j.cclet.2022.03.063openalex-snapshot
Thiocytochalasins A−D, four sulfur-containing cytochalasans from an endophytic fungus Phoma multirostrata XJ-2-1
inferred← citeshttps://doi.org/10.1016/j.cclet.2022.05.030openalex-snapshot
Vercytochalasins A and B: Two unprecedented biosynthetically related cytochalasins from the deep-sea-sourced endozoic fungus Curvularia verruculosa
inferred← citeshttps://doi.org/10.1016/j.cclet.2024.110252openalex-snapshot
Discovery and enantioselective total synthesis of antitumor agent asperfilasin A via a regio- and diastereoselective Nazarov cyclization
inferred← citeshttps://doi.org/10.1016/j.cclet.2026.112499openalex-snapshot
Endophytic and soilborne Chaetomium: A promising fungal resource for producing and biosynthesizing structurally and biologically diverse indole alkaloids
inferred← citeshttps://doi.org/10.1016/j.chempr.2020.11.010openalex-snapshot
Biosynthetically Inspired Divergent Syntheses of Merocytochalasans
inferred← citeshttps://doi.org/10.1016/j.cub.2025.08.023openalex-snapshot
Differential interference with actin-binding protein function by acute cytochalasin B
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112502openalex-snapshot
Anticancer fungal natural products: Mechanisms of action and biosynthesis
inferred← citeshttps://doi.org/10.1016/j.ejmech.2025.118502openalex-snapshot
The potential of cytochalasins and other cytochalasans as drugs targeting cancer cell invasiveness and metastasis
inferred← citeshttps://doi.org/10.1016/j.fbr.2026.100471openalex-snapshot
Dematophora necatrix: From taxonomy to molecular advances
inferred← citeshttps://doi.org/10.1016/j.fitote.2013.12.022openalex-snapshot
Chaetoglobosin Y, a new cytochalasan from Chaetomium globosum
inferred← citeshttps://doi.org/10.1016/j.fitote.2014.04.009openalex-snapshot
Stereochemical determination of new cytochalasans from the plant endophytic fungus Trichoderma gamsii
inferred← citeshttps://doi.org/10.1016/j.fitote.2018.11.010openalex-snapshot
Cytotoxic seco-cytochalasins from an endophytic Aspergillus sp. harbored in Pinellia ternata tubers
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104253openalex-snapshot
Cytotoxic 19,20-epoxycytochalasans from endophytic fungus Xylaria cf. curta
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104278openalex-snapshot
Cytotoxic cytochalasans from fungus Xylaria longipes
inferred← citeshttps://doi.org/10.1016/j.fitote.2020.104611openalex-snapshot
Cytochalasans from endophytic fungus Diaporthe sp. SC-J0138
inferred← citeshttps://doi.org/10.1016/j.fitote.2021.104874openalex-snapshot
Salchaetoglobosins A and B: Cytochalasan alkaloids from Chaetomium globosum D38, a fungus derived from Salvia miltiorrhiza
inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105434openalex-snapshot
Unreported Cytochalasins from an Acid-Mediated Transformation of Cytochalasin J Isolated from Diaporthe Cf. Ueckeri
inferred← citeshttps://doi.org/10.1016/j.funbio.2020.10.010openalex-snapshot
Functional analysis of a chaetoglobosin A biosynthetic regulator in Chaetomium globosum
inferred← citeshttps://doi.org/10.1016/j.funbio.2020.11.008openalex-snapshot
Requirement of LaeA for sporulation, pigmentation and secondary metabolism in Chaetomium globosum
inferred← citeshttps://doi.org/10.1016/j.micres.2020.126646openalex-snapshot
An actin depolymerizing agent 19,20-epoxycytochalasin Q of Xylaria sp. BCC 1067 enhanced antifungal action of azole drugs through ROS-mediated cell death in yeast
inferred← citeshttps://doi.org/10.1016/j.microb.2025.100628openalex-snapshot
In silico analysis of entomopathogenic fungal (Metarhizium spp. and Beauveria bassiana) metabolites for Coptotermes spp. (Blattodea: Rhinotermitidae) control
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140274openalex-snapshot
Chemical constituents from a soil fungus Xylaria sp. Y01 and their anticancer potential
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145974openalex-snapshot
Cytotoxic ɑ-pyrone derivatives and cytochalasins from the soil-derived fungus Pleosporales sp. DWS-632
inferred← citeshttps://doi.org/10.1016/j.mrrev.2021.108372openalex-snapshot
Lymphocyte micronuclei frequencies in skin, haematological, prostate, colorectal and esophageal cancer cases: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.phytochem.2018.09.004openalex-snapshot
Armochaetoglasins A–I: Cytochalasan alkaloids from fermentation broth of Chaetomium globosum TW1-1 by feeding L-tyrosine
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112952openalex-snapshot
Asporychalasin, a bioactive cytochalasan with an unprecedented 6/6/11 skeleton from the Red Sea sediment Aspergillus oryzae
inferred← citeshttps://doi.org/10.1016/j.phytochem.2023.113939openalex-snapshot
Chaepseubakerins A–J, ten undescribed cytotoxic [11]-chaetoglobosins from an endophytic fungus Pseudeurotium bakeri
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114103openalex-snapshot
Rosellichalasins A–H, cytotoxic cytochalasans from the endophytic fungus Rosellinia sp. Glinf021
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114340openalex-snapshot
Cytochalasins and orsellinic acid derivatives with cytotoxicity from the soil-derived fungus Trichocladium asperum
inferred← citeshttps://doi.org/10.1016/j.phytochem.2025.114655openalex-snapshot
Cytochalasins from the marine-derived fungus Acremonium implicatum DFFSCS001 and their anti-inflammatory activities
inferred← citeshttps://doi.org/10.1016/j.phytol.2014.06.014openalex-snapshot
An antibacterial cytochalasin derivative from the marine-derived fungus Diaporthaceae sp. PSU-SP2/4
inferred← citeshttps://doi.org/10.1016/j.phytol.2015.06.007openalex-snapshot
Cytotoxic metabolites from Botryotinia fuckeliana A-S-3: An endophytic fungus from Ajuga decumbens
inferred← citeshttps://doi.org/10.1016/j.phytol.2015.09.004openalex-snapshot
Two new cytochalasins from an endophytic fungus, KL-1.1 isolated from Psidium guajava leaves
inferred← citeshttps://doi.org/10.1016/j.phytol.2016.07.027openalex-snapshot
Cytochalasins from mangrove endophytic fungi Phomopsis spp. xy21 and xy22
inferred← citeshttps://doi.org/10.1016/j.phytol.2019.05.002openalex-snapshot
Two new cytochalasans from the marine sediment-derived fungus Westerdykella dispersa and their antibacterial activities
inferred← citeshttps://doi.org/10.1016/j.phytol.2026.104119openalex-snapshot
Structural diversity and cytotoxic secondary metabolites from the endophytic fungus Chaetomium globosum
inferred← citeshttps://doi.org/10.1016/j.simyco.2021.100118openalex-snapshot
Secondary metabolite biosynthetic diversity in the fungal family Hypoxylaceae and Xylaria hypoxylon
inferred← citeshttps://doi.org/10.1016/j.taap.2022.115971openalex-snapshot
Cytochalasin Q exerts anti-melanoma effect by inhibiting creatine kinase B
inferred← citeshttps://doi.org/10.1016/j.tchem.2022.100022openalex-snapshot
Collective total syntheses of cytochalasans and merocytochalasans
inferred← citeshttps://doi.org/10.1016/j.tet.2011.09.079openalex-snapshot
Identification of an unexpected 2-oxonia[3,3]sigmatropic rearrangement/aldol pathway in the formation of oxacyclic rings. Total synthesis of (+)-aspergillin PZ
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131475openalex-snapshot
Phomopsisins A–C: Three new cytochalasans from the plant endophytic fungus Phomopsis sp. sh917
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.11.084openalex-snapshot
New azaphilones from Chaetomium globosum isolated from the built environment
inferred← citeshttps://doi.org/10.1016/j.tetlet.2013.03.120openalex-snapshot
Biosynthetic assembly of cytochalasin backbone
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.01.030openalex-snapshot
Periconiasin G, a new cytochalasan with unprecedented 7/6/5 tricyclic ring system from the endophytic fungus Periconia sp.
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.11.038openalex-snapshot
Periconiasins I and J, two new cytochalasans from an endophytic fungus Periconia sp.
inferred← citeshttps://doi.org/10.1016/j.tetlet.2017.04.071openalex-snapshot
Aspochalazine A, a novel polycyclic aspochalasin from the fungus Aspergillus sp. Z4
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.03.077openalex-snapshot
Cytotoxic cytochalasans from Aspergillus flavipes PJ03-11 by OSMAC method
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.150952openalex-snapshot
Cytochalasins D1 and C1, unique cytochalasans from endophytic fungus Xylaria cf. curta
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151204openalex-snapshot
Features of oxa-bridge cleavage in hexahydro-3a,6-epoxyisoindol-1(4H)-ones: A concise method to access acetylisoindolones possessing anti-viral activity
inferred← citeshttps://doi.org/10.1016/j.tetlet.2020.151838openalex-snapshot
Four cytochalasin alkaloids produced by Chaetomium globosum
inferred← citeshttps://doi.org/10.1016/j.tiv.2017.05.015openalex-snapshot
Inflammation-associated gene expression in RAW 264.7 macrophages induced by toxins from fungi common on damp building materials
inferred← citeshttps://doi.org/10.1016/j.tranon.2015.06.003openalex-snapshot
Preparation, In Vivo Administration, Dose-Limiting Toxicities, and Antineoplastic Activity of Cytochalasin B
inferred← citeshttps://doi.org/10.1016/j.ymben.2011.09.008openalex-snapshot
Identification and engineering of the cytochalasin gene cluster from Aspergillus clavatus NRRL 1
inferred← citeshttps://doi.org/10.1016/s1875-5364(25)60880-6openalex-snapshot
Bioactivity-guided discovery of antiviral templichalasins A‒C from the endophytic fungus Aspergillus templicola
inferred← citeshttps://doi.org/10.1021/acs.accounts.1c00459openalex-snapshot
Biomimetic Synthesis of Natural Products: A Journey To Learn, To Mimic, and To Be Better
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00478openalex-snapshot
Oxidative Cyclization in Natural Product Biosynthesis
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c08868openalex-snapshot
Structural Diversity of Glycosylated Cytochalasins and Congeners from the Endophytic Fungus Trichoderma harzianum MLJ-4 with Anti-NSCLC Activity
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c10857openalex-snapshot
Oat Leaf Diseases: Secondary Metabolites of Pathogenic Fungi and Infected Plants and Their Toxicity
inferred← citeshttps://doi.org/10.1021/acs.jafc.9b00273openalex-snapshot
Cytochalasins and an Abietane-Type Diterpenoid with Allelopathic Activities from the Endophytic Fungus Xylaria Species
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c01202openalex-snapshot
Evolution-Based Discovery of Polyketide Acylated Valine from a Cytochalasin-Like Gene Cluster in Simplicillium lamelliciola HDN13430
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00676openalex-snapshot
Comprehensive Cell Biological Investigation of Cytochalasin B Derivatives with Distinct Activities on the Actin Network
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c01296openalex-snapshot
Derailment of the Biosynthesis via an Acid-Mediated Intramolecular Cyclo-rearrangement Leads to a Novel Cytochalasin Skeleton
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c00180openalex-snapshot
Cytochalasins from the Sponge-Derived Fungus Aspergillus templicola and Their Biological Activities
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6b00333openalex-snapshot
Overexpression of the Global Regulator LaeA in Chaetomium globosum Leads to the Biosynthesis of Chaetoglobosin Z
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.6c00375openalex-snapshot
Polycyclic-Fused Cytochalasins with Anti-Liver Fibrosis Activity Produced by the Endophytic Fungus Trichoderma harzianum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00770openalex-snapshot
Lichen Biosynthetic Gene Clusters Part II: Homology Mapping Suggests a Functional Diversity
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00110openalex-snapshot
Cytochalasans Produced by the Coculture of Aspergillus flavipes and Chaetomium globosum
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00016openalex-snapshot
Cysteine Residue Containing Merocytochalasans and 17,18-seco-Aspochalasins from Aspergillus micronesiensis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00512openalex-snapshot
Flavipesines A and B and Asperchalasines E–H: Cytochalasans and Merocytochalasans from Aspergillus flavipes
inferred← citeshttps://doi.org/10.1021/acs.joc.1c00425openalex-snapshot
Bisaspochalasins D and E: Two Heterocycle-Fused Cytochalasan Homodimers from an Endophytic Aspergillus flavipes
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01757openalex-snapshot
Stereocontrolled Synthesis of Enantiopure cis-Fused Octahydroisoindolones via Chiral Oxazoloisoindolone Lactams
inferred← citeshttps://doi.org/10.1021/acs.joc.3c01515openalex-snapshot
Boerelasins A–D, Four Unprecedented Cytochalasins from the Endophytic Fungus Boeremia Exigua
inferred← citeshttps://doi.org/10.1021/acs.joc.7b01793openalex-snapshot
Cytochalasins from an Australian Marine Sediment-Derived Phomopsis sp. (CMB-M0042F): Acid-Mediated Intramolecular Cycloadditions Enhance Chemical Diversity
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00440openalex-snapshot
Amiaspochalasins A–H, Undescribed Aspochalasins with a C-21 Ester Carbonyl from Aspergillus micronesiensis
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01846openalex-snapshot
Formal Total Synthesis of Pericoannosin A
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02860openalex-snapshot
Bisaspochalasins A–C: Three Cytochalasan Homodimers with Highly Fused Ring System from an Endophytic Aspergillus flavipes
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03623openalex-snapshot
Pchaeglobolactone A, Spiropchaeglobosin A, and Pchaeglobosals A and B: Four Rearranged Cytochalasans from Chaetomium globosum P2-2-2
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01922openalex-snapshot
Synthesis of a Biomimetic Tetracyclic Precursor of Aspochalasins and Formal Synthesis of Trichoderone A
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01039openalex-snapshot
Genome Mining of a Fungal Polyketide Synthase–Nonribosomal Peptide Synthetase Hybrid Megasynthetase Pathway to Synthesize a Phytotoxic N-Acyl Amino Acid
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02123openalex-snapshot
Pericoannosin A, a Polyketide Synthase–Nonribosomal Peptide Synthetase Hybrid Metabolite with New Carbon Skeleton from the Endophytic Fungus Periconia sp.
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00214openalex-snapshot
Phomopchalasins A and B, Two Cytochalasans with Polycyclic-Fused Skeletons from the Endophytic FungusPhomopsissp. shj2
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00352openalex-snapshot
Bioinspired Synthesis of Curtachalasin A and Δ 6,12 -Curtachalasin N Enabled by Tandem Transannular Epoxyalkene Cyclization and α-Ketol Rearrangement
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c03240openalex-snapshot
Boereguasins A–D, Cytochalasins from Boeremia exigua with Differential MAPK/NF-κB Inhibition
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00559openalex-snapshot
Integration of Chemical, Genetic, and Bioinformatic Approaches Delineates Fungal Polyketide–Peptide Hybrid Biosynthesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01534openalex-snapshot
Identification and Heterologous Production of a Benzoyl-Primed Tricarboxylic Acid Polyketide Intermediate from the Zaragozic Acid A Biosynthetic Pathway
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02146openalex-snapshot
Aspergilasines A–D: Four Merocytochalasans with New Carbon Skeletons from Aspergillus flavipes QCS12
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01243openalex-snapshot
Aureochaeglobosins A–C, Three [4 + 2] Adducts of Chaetoglobosin and Aureonitol Derivatives from Chaetomium globosum
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02942openalex-snapshot
Cytochathiazines A–C: Three Merocytochalasans with a 2 H -1,4-Thiazine Functionality from Coculture of Chaetomium globosum and Aspergillus flavipes
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b03110openalex-snapshot
Curtachalasins A and B, Two Cytochalasans with a Tetracyclic Skeleton from the Endophytic Fungus Xylaria curta E10
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b04066openalex-snapshot
Amichalasines A–C: Three Cytochalasan Heterotrimers from Aspergillus micronesiensis PG-1
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b04129openalex-snapshot
Intramolecular Diels–Alder Cycloaddition Approach toward the cis-Fused Δ5,6-Hexahydroisoindol-1-one Core of Cytochalasins
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00015openalex-snapshot
Cytochalasans from the Endophytic Fungus Xylaria cf. curta with Resistance Reversal Activity against Fluconazole-Resistant Candida albicans
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01065openalex-snapshot
Chamiside A, a Cytochalasan with a Tricyclic Core Skeleton from the Endophytic Fungus Chaetomium nigricolor F5
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01344openalex-snapshot
Targeted Gene Inactivations Expose Silent Cytochalasans in Magnaporthe grisea NI980
showing the first 200 of 389 · page through all 389
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.