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Immunomodulatory Constituents from an Ascomycete, Chaetomium s eminudum

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1021/ja00437a074openalex-snapshot
The structure of chetomin
inferredcites →https://doi.org/10.1021/np010152nopenalex-snapshot
Immunomodulatory Constituents from an Ascomycete, Eupenicillium crustaceum, and Revised Absolute Structure of Macrophorin D
inferredcites →https://doi.org/10.1139/m81-119openalex-snapshot
Mycotoxin production by Chaetomium spp. and related fungi
inferredcites →https://doi.org/10.1248/cpb.41.654openalex-snapshot
Identification of Immunosuppressive Components of a Mushroom, Lactarius flavidulus.
inferredcites →https://doi.org/10.1248/cpb.43.547openalex-snapshot
Isolation of Some Immunosuppressive Components from an Ascomycete, Gelasinospora multiforis
inferredcites →https://doi.org/10.1248/cpb.48.1436openalex-snapshot
Immunomodulatory Constituents from an Ascomycete, Emericella aurantio-brunnea.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Chaetomium: Goldmine for Sustainable Agriculture
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Low-nanomolar chetomin in human skin cells: Preserved viability and wound closure, reduced basal IL-6 and IL-1β release, and preliminary tolerability in Galleria mellonella
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Inhibition of VEGF transcription through blockade of the hypoxia inducible factor-1α–p300 interaction by a small molecule
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Cytotoxic indole diketopiperazines from the deep sea-derived fungus Acrostalagmus luteoalbus SCSIO F457
inferred← citeshttps://doi.org/10.1016/j.cclet.2010.05.023openalex-snapshot
Chromones from an ascomycete, Chaetomium aureus
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
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Small molecule blockade of transcriptional coactivation of the hypoxia-inducible factor pathway
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Small-Molecule Reactivation of Mutant p53 to Wild-Type-like p53 through the p53-Hsp40 Regulatory Axis
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Ochrolines A-C, three new indole diketopiperazines from cultures of endophytic fungi Bionectria ochroleuca SLJB-2
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Aspergillus-derived indole diketopiperazines (IDKPs): chemical diversity, biosynthetic logics, and therapeutic potential
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Enantioselective organocatalytic α-sulfenylation of substituted diketopiperazines
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DABCO/AgOAc cooperatively catalyzed α-sulfenylation of isocyanoacetates with N-(sulfanyl)succinimides
inferred← citeshttps://doi.org/10.1021/acs.jafc.6b01772openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c00434openalex-snapshot
Shielding Effects of Aromatic (Indole) Ring for Structural Analysis
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00215openalex-snapshot
UPLC-Q-TOF-MS/MS-Based Targeted Discovery of Chetomin Analogues from Chaetomium cochliodes
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00239openalex-snapshot
Chetocochliodins A‑I, Epipoly(thiodioxopiperazines) from Chaetomium cochliodes
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01283openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00304openalex-snapshot
Highly Photosensitive Poly-Sulfur-Bridged Chetomin Analogues from Chaetomium cochliodes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01770openalex-snapshot
A Modular Construction of Epidithiodiketopiperazines
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Palladium-Catalyzed Synthesis of 3-Acylated Indoles Involving Oxidative Cross-Coupling of Indoles with α-Amino Carbonyl Compounds
inferred← citeshttps://doi.org/10.1021/jo501881yopenalex-snapshot
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Epicoccins A–D, Epipolythiodioxopiperazines from a Cordyceps-Colonizing Isolate of Epicoccum nigrum
inferred← citeshttps://doi.org/10.1021/np3000443openalex-snapshot
Cytotoxic Metabolites from the Antarctic Psychrophilic Fungus Oidiodendron truncatum
inferred← citeshttps://doi.org/10.1021/np300894yopenalex-snapshot
Leporizines A–C: Epithiodiketopiperazines Isolated from an Aspergillus Species
inferred← citeshttps://doi.org/10.1021/np400045zopenalex-snapshot
Roussoellols A and B, Tetracyclic Fusicoccanes from Roussoella hysterioides
inferred← citeshttps://doi.org/10.1021/np5007235openalex-snapshot
Indole Alkaloids from Chaetomium globosum
inferred← citeshttps://doi.org/10.1021/ol400444gopenalex-snapshot
Indoles Synthesized from Amines via Copper Catalysis
inferred← citeshttps://doi.org/10.1021/ol801028eopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/d2ob02220fopenalex-snapshot
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inferred← citeshttps://doi.org/10.1039/np9900700269openalex-snapshot
Marine natural products
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Two new diketopiperazines from the tin mine tailings-derived fungus Schizophyllum commune YIM DT 10058
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Novel indole diketopiperazine stereoisomers from a marine-derived fungus Aspergillus sp.
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Polymorphism and phase transition behavior of 6,6′-bis(chloromethyl)-1,1′,4,4′-tetramethyl-3,3′-(p-phenylenedimethylene)bis(piperazine-2,5-dione)
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Diethyltrans-2,5-bis(4-methoxybenzylsulfanyl)-1,4-dimethyl-3,6-dioxopiperazine-2,5-carboxylate
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Hypoxia‐inducible factor‐1α blocks differentiation of malignant gliomas
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inferred← citeshttps://doi.org/10.1248/cpb.c15-00525openalex-snapshot
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One-pot synthesis of indole-fused diketopiperazine through an Ugi 4-CR condensation and N-annulation under mild conditions
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inferred← citeshttps://doi.org/10.3390/biom13081191openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md17100551openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md18030132openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md18070338openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules22122026openalex-snapshot
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