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Cytotoxic Constituents of the Lichen Diploicia canescens
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/chem.200800035openalex-snapshot
New Mono‐ and Dimeric Members of the Secalonic Acid Family: Blennolides A–G Isolated from the Fungus Blennoria sp.
inferredcites →https://doi.org/10.1007/bf02977469openalex-snapshot
Secalonic acid D; A cytotoxic constituent from marine lichen-derived fungusGliocladium sp. T31
inferredcites →https://doi.org/10.1016/0022-1759(83)90303-4openalex-snapshot
Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
inferredcites →https://doi.org/10.1016/0040-4020(70)85006-2openalex-snapshot
The isolation, structure and absolute configuration of secalonic acid D, the toxic metabolite of Penicillium oxalicum
inferredcites →https://doi.org/10.1016/s0031-9422(00)80821-3openalex-snapshot
The isolation of methyl β-orsellinate from Stereocaulon alpinum and comments on the isolation of 4,6-dihydroxy-2- methoxy-3-methylacetophenone from stereocaulon species
inferredcites →https://doi.org/10.1021/jo00422a042openalex-snapshot
Secalonic acids D and F are toxic metabolites of Aspergillus aculeatus
inferredcites →https://doi.org/10.1039/b606983popenalex-snapshot
Metabolic diversity of lichen-forming ascomycetous fungi: culturing, polyketide and shikimatemetabolite production, and PKS genes
inferredcites →https://doi.org/10.1039/p19760000147openalex-snapshot
Depsidone synthesis. Part II. Diploicin and gangaleoidin
inferredcites →https://doi.org/10.1039/p19810000849openalex-snapshot
Depsidone synthesis. Part 15. New metabolites of the lichen Buellia canescens(Dicks.) De Not: novel phthalide catabolites of depsidones
inferredcites →https://doi.org/10.1039/p19810000855openalex-snapshot
Depsidone synthesis. Part 16. Benzophenone–grisa-3′,5′-diene-2′,3-dione–depsidone interconversion: a new theory of depsidone biosynthesis
inferredcites →https://doi.org/10.1039/p19830000413openalex-snapshot
Scensidin, a new depsidone from the lichen Buellia canescens(Dicks.) De Not
inferredcites →https://doi.org/10.1055/s-2004-827240openalex-snapshot
Cytotoxic Activity of Compounds from the Lichen:Cladonia convoluta
inferredcites →https://doi.org/10.1071/ch9900197openalex-snapshot
New Chlorine-Containing Depsidones From Lichens
inferredcites →https://doi.org/10.7164/antibiotics.32.1256openalex-snapshot
Biosynthetic relationships among the secalonic acids. Isolation of emodin, endocrocin and secalonic acids from Pyrenochaeta terrestris and Aspergillus aculeatus.
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.2018.09.011zenodo-depositor-declared
Tissue-specific localization of polyketide synthase and other associated genes in the lichen, Cladonia rangiferina, using laser microdissection
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112535zenodo-depositor-declared
Lichen-associated bacteria transform antibacterial usnic acid to products of lower antibiotic activity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113264zenodo-depositor-declared
Undescribed diphenyl ethers betaethrins A-I from a desert plant endophytic strain of the fungus Phoma betae A.B. Frank (Didymellaceae)
inferred← citeshttps://doi.org/10.1002/cmdc.201200345openalex-snapshot
Discovery of Depsides and Depsidones from Lichen as Potent Inhibitors of Microsomal Prostaglandin E2 Synthase‐1 Using Pharmacophore Models
inferred← citeshttps://doi.org/10.1002/ejoc.201600252openalex-snapshot
Cyaneodimycin, a Bioactive Compound Isolated from the Culture of Streptomyces cyaneofuscatus Associated with Lichina confinis
inferred← citeshttps://doi.org/10.1002/hlca.201300447openalex-snapshot
Biosynthesis of Bromoroquefortines in a High Saline Medium by Penicillium chrysogenum, a Terrestrial Endophyte Collected from Coffea arabica
inferred← citeshttps://doi.org/10.1002/pca.3008openalex-snapshot
Efficiency and selectivity of ionic liquids in microwave‐assisted extraction of major lichen phenolic compounds: a scalable process with recycling of ionic liquids
inferred← citeshttps://doi.org/10.1007/978-3-031-26629-4_1openalex-snapshot
Naturally Occurring Organohalogen Compounds—A Comprehensive Review
inferred← citeshttps://doi.org/10.1007/978-3-031-30037-0_29-1openalex-snapshot
Isolation and Identification of Lichen Substances for Biological and Ecological Roles
inferred← citeshttps://doi.org/10.1007/978-3-031-51158-5_29openalex-snapshot
Isolation and Identification of Lichen Substances for Biological and Ecological Roles
inferred← citeshttps://doi.org/10.1007/978-3-642-37922-2_80openalex-snapshot
Lichen: A Potential Anticancer Officinal Resource
inferred← citeshttps://doi.org/10.1007/978-981-13-7607-8_7openalex-snapshot
Immunomodulatory and Therapeutic Potential of Marine Flora Products in the Treatment of Cancer
inferred← citeshttps://doi.org/10.1007/s11101-010-9200-2openalex-snapshot
Photosynthetic marine organisms as a source of anticancer compounds
inferred← citeshttps://doi.org/10.1007/s11101-011-9215-3openalex-snapshot
Advanced methods for the study of the chemistry and the metabolism of lichens
inferred← citeshttps://doi.org/10.1007/s11101-020-09701-9openalex-snapshot
Fungal metabolites as anti-diabetic agents: emphasis on PTP1B inhibitors
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104449openalex-snapshot
Eumitrins C-E: Structurally diverse xanthone dimers from the vietnamese lichen Usnea baileyi
inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2012.03.005openalex-snapshot
Photoprotective capacities of lichen metabolites: A joint theoretical and experimental study
inferred← citeshttps://doi.org/10.1016/j.phymed.2016.02.012openalex-snapshot
Secondary metabolites from cetrarioid lichens: Chemotaxonomy, biological activities and pharmaceutical potential
inferred← citeshttps://doi.org/10.1016/j.phytochem.2017.10.005openalex-snapshot
Chemical analysis of the Alphaproteobacterium strain MOLA1416 associated with the marine lichen Lichina pygmaea
inferred← citeshttps://doi.org/10.1016/j.ympev.2018.02.013openalex-snapshot
Evolutionary history of ergot with a new infrageneric classification (Hypocreales: Clavicipitaceae: Claviceps)
inferred← citeshttps://doi.org/10.1021/acs.analchem.5b02531openalex-snapshot
Matrix-Free UV-Laser Desorption Ionization Mass Spectrometry as a Versatile Approach for Accelerating Dereplication Studies on Lichens
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00264openalex-snapshot
Insights into Ergochromes of the Plant Pathogen Claviceps purpurea
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00277openalex-snapshot
CASE-DFT Structure Elucidation of Proton-Deficient Chlorodepsidones from the Indonesian Lichen Teloschistes flavicans and Structure Revision of Flavicansone
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5b01073openalex-snapshot
Minor Pyranonaphthoquinones from the Apothecia of the Lichen Ophioparma ventosa
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00340openalex-snapshot
α-Pyrone and Sterol Constituents of Penicillium aurantiacobrunneum, a Fungal Associate of the Lichen Niebla homalea
inferred← citeshttps://doi.org/10.1021/cr100446hopenalex-snapshot
Xanthones from Fungi, Lichens, and Bacteria: The Natural Products and Their Synthesis
inferred← citeshttps://doi.org/10.1021/jo3018318openalex-snapshot
Copper(I)-Catalyzed Intramolecular O-Arylation for the Synthesis of 2,3,4,9-Tetrahydro-1H-xanthen-1-ones with Low Loads of CuCl
inferred← citeshttps://doi.org/10.1038/ja.2012.110openalex-snapshot
Antifouling and antibacterial polyketides from marine gorgonian coral-associated fungus Penicillium sp. SCSGAF 0023
inferred← citeshttps://doi.org/10.1039/c2md20199bopenalex-snapshot
Diaryl ether derivatives as anticancer agents – a review
inferred← citeshttps://doi.org/10.1039/c3np70064jopenalex-snapshot
UV-protectant metabolites from lichens and their symbiotic partners
inferred← citeshttps://doi.org/10.1039/c7cs00431aopenalex-snapshot
Secondary metabolism in the lichen symbiosis
inferred← citeshttps://doi.org/10.1039/c8ob01280fopenalex-snapshot
Tsavoenones A–C: unprecedented polyketides with a 1,7-dioxadispiro[4.0.4.4]tetradecane core from the lichen Parmotrema tsavoense
inferred← citeshttps://doi.org/10.1055/a-1203-0623openalex-snapshot
Salazinic Acid-Derived Depsidones and Diphenylethers with α-Glucosidase Inhibitory Activity from the Lichen Parmotrema dilatatum
inferred← citeshttps://doi.org/10.1080/14786419.2013.879305openalex-snapshot
Four chlorinated depsidones from a seaweed-derived strain of Aspergillus unguis and their new biological activities
inferred← citeshttps://doi.org/10.1080/19443994.2015.1094424openalex-snapshot
Biosorption performance of the lichen biomass (Diploicia canescens) for the removal of nickel from aqueous solutions
inferred← citeshttps://doi.org/10.1099/acmi.0.000536.v4openalex-snapshot
Evidence for some antimicrobial properties of English churchyard lichens
inferred← citeshttps://doi.org/10.1107/s1600536810010718openalex-snapshot
2-(4-Bromophenyl)-6-methyl-4H-1-benzopyran-4-one (4′-bromo-6-methylflavone)
inferred← citeshttps://doi.org/10.1134/s1990750825601201openalex-snapshot
Cytotoxic and Cytostatic Properties of Lichen Depsidones (Review)
inferred← citeshttps://doi.org/10.14712/fb2014060020089openalex-snapshot
Effects of Depsidones from Hypogymnia physodes on HeLa Cell Viability and Growth
inferred← citeshttps://doi.org/10.1639/0007-2745-113.3.690openalex-snapshot
Recent literature on lichens—218
inferred← citeshttps://doi.org/10.2174/1389201021666200504114515openalex-snapshot
Cytotoxic and Antibiotic Potential of Secondary Metabolites from the Lichen Umbilicaria muhlenbergii
inferred← citeshttps://doi.org/10.2174/9789815136807123010007openalex-snapshot
An Introduction to Diabetes Drug Discovery in Biomedical Industry through Artificial Intelligence, Using Lichens' Secondary Metabolites
inferred← citeshttps://doi.org/10.2903/sp.efsa.2017.en-1274openalex-snapshot
Database on the taxonomical characterisation and potential toxigenic capacities of microorganisms used for the industrial production of food enzymes and feed additives, which do not have a recommendation for Qualified Presumption of Safety
inferred← citeshttps://doi.org/10.3390/molecules21030294openalex-snapshot
Xanthones of Lichen Source: A 2016 Update
inferred← citeshttps://doi.org/10.3390/molecules22030371openalex-snapshot
Isolation and Structure Identification of Novel Brominated Diketopiperazines from Nocardia ignorata—A Lichen-Associated Actinobacterium
inferred← citeshttps://doi.org/10.3390/molecules23081951openalex-snapshot
tert-Butylphenolic Derivatives from Paenibacillus odorifer—A Case of Bioconversion
inferred← citeshttps://doi.org/10.3390/molecules27103157openalex-snapshot
Halogenation in Fungi: What Do We Know and What Remains to Be Discovered?
inferred← citeshttps://doi.org/10.3390/plants12040694openalex-snapshot
Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens
inferred← citeshttps://doi.org/10.3390/toxins11080439openalex-snapshot
Ergochromes: Heretofore Neglected Side of Ergot Toxicity
inferred← citeshttps://doi.org/10.70675/7eddce04z77d6z40b3z99d7z803b1c03911dopenalex-snapshot
Recherche de molécules antimicrobiennes d'origine lichénique : Etude phytochimique de trois lichens & approche synthétique de deux composés actifs
inferred← citeshttps://doi.org/10.70675/923a4da5zf9f1z45d9zab8fz5133c84e5aa6openalex-snapshot
Analyses de lichens par spectrométrie de masse : déréplication et histolocalisation
inferred← citeshttps://doi.org/10.70675/c0425229z8b5ez4b1bzb4bazf3ae38a51871openalex-snapshot
Discovery of active secondary metabolites from Paenibacillus odorifer, a lichen-associated bacterium
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