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Antiviral Alkaloids Produced by the Mangrove-Derived Fungus Cladosporium sp. PJX-41
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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/ejoc.201201220openalex-snapshot
Alkaloids from the Sponge‐Associated Fungus Aspergillus sp.
inferredcites →https://doi.org/10.1016/j.antiviral.2008.10.006openalex-snapshot
Aurintricarboxylic acid inhibits influenza virus neuraminidase
inferredcites →https://doi.org/10.1016/j.bmcl.2012.03.044openalex-snapshot
Pyronepolyene C-glucosides with NF-κB inhibitory and anti-influenza A viral (H1N1) activities from the sponge-associated fungus Epicoccum sp. JJY40
inferredcites →https://doi.org/10.1016/j.bmcl.2013.01.051openalex-snapshot
Aspulvinones from a mangrove rhizosphere soil-derived fungus Aspergillus terreus Gwq-48 with anti-influenza A viral (H1N1) activity
inferredcites →https://doi.org/10.1016/j.phytochem.2011.04.014openalex-snapshot
Antiviral isoindolone derivatives from an endophytic fungus Emericella sp. associated with Aegiceras corniculatum
inferredcites →https://doi.org/10.1016/j.tet.2006.11.074openalex-snapshot
Aspergiolide A, a novel anthraquinone derivative with naphtho[1,2,3-de]chromene-2,7-dione skeleton isolated from a marine-derived fungus Aspergillus glaucus
inferredcites →https://doi.org/10.1016/j.tet.2008.06.013openalex-snapshot
Seven new prenylated indole diketopiperazine alkaloids from holothurian-derived fungus Aspergillus fumigatus
inferredcites →https://doi.org/10.1016/j.tet.2012.02.024openalex-snapshot
Sartorymensin, a new indole alkaloid, and new analogues of tryptoquivaline and fiscalins produced by Neosartorya siamensis (KUFC 6349)
inferredcites →https://doi.org/10.1016/j.tetlet.2007.06.089openalex-snapshot
Synthesis of (−)-lapatin B
inferredcites →https://doi.org/10.1016/s0040-4039(01)85965-7openalex-snapshot
The absolute configuration of nortryptoquivaline
inferredcites →https://doi.org/10.1016/s0040-4039(01)90633-1openalex-snapshot
σ-carbon participation in the solvolysis of organomercurials
inferredcites →https://doi.org/10.1016/s0040-4039(01)91189-xopenalex-snapshot
Total synthesis of (+)-tryptoquivaline
inferredcites →https://doi.org/10.1021/bi2004922openalex-snapshot
Unraveling Terminal C-Domain-Mediated Condensation in Fungal Biosynthesis of Imidazoindolone Metabolites
inferredcites →https://doi.org/10.1021/ja00836a045openalex-snapshot
Tryptoquivaline and tryptoquivalone, two tremorgenic metabolites of Aspergillus clavatus
inferredcites →https://doi.org/10.1021/ja1101085openalex-snapshot
Fungal Indole Alkaloid Biosynthesis: Genetic and Biochemical Investigation of the Tryptoquialanine Pathway inPenicillium aethiopicum
inferredcites →https://doi.org/10.1021/jf020398dopenalex-snapshot
Penicillium digitatum Metabolites on Synthetic Media and Citrus Fruits
inferredcites →https://doi.org/10.1021/jo00422a015openalex-snapshot
Four new mycotoxins of Aspergillus clavatus related to tryptoquivaline
inferredcites →https://doi.org/10.1021/jo0508043openalex-snapshot
Three-Component One-Pot Total Syntheses of Glyantrypine, Fumiquinazoline F, and Fiscalin B Promoted by Microwave Irradiation
inferredcites →https://doi.org/10.1021/jo9914364openalex-snapshot
Total Synthesis of the Fumiquinazoline Alkaloids: Solution-Phase Studies1
inferredcites →https://doi.org/10.1021/np980056vopenalex-snapshot
UV-Guided Isolation of Alantrypinone, a Novel Penicillium Alkaloid
inferredcites →https://doi.org/10.1021/ol802089popenalex-snapshot
Relative and Absolute Stereochemistry of Quinadoline B, an Inhibitor of Lipid Droplet Synthesis in Macrophages
inferredcites →https://doi.org/10.1021/ol901304yopenalex-snapshot
Brevianamide J, A New Indole Alkaloid Dimer from Fungus Aspergillus versicolor
inferredcites →https://doi.org/10.1039/b301926hopenalex-snapshot
Marine-derived fungi: a chemically and biologically diverse group of microorganisms
inferredcites →https://doi.org/10.1039/b607254mopenalex-snapshot
Marine natural products of fungal origin
inferredcites →https://doi.org/10.1039/c2ob26757hopenalex-snapshot
Diketopiperazine alkaloids from a mangrove rhizosphere soil derived fungus Aspergillus effuses H1-1
inferredcites →https://doi.org/10.1039/p19810001495openalex-snapshot
Reactions of pyryliums with mono- and asym-di-substituted hydrazines
inferredcites →https://doi.org/10.1039/p19920001495openalex-snapshot
Glyantrypine, a novel anthranilic acid-containing metabolite of Aspergillus clavatus
inferredcites →https://doi.org/10.1039/p19950002345openalex-snapshot
Fumiquinazolines A–G, novel metabolites of a fungus separated from a Pseudolabrus marine fish
inferredcites →https://doi.org/10.1111/j.1574-6968.1992.tb05266.xopenalex-snapshot
Biosynthesis of glyantrypine byAspergillus clavatus
inferredcites →https://doi.org/10.1248/cpb.44.1843openalex-snapshot
Isolation of New Tremorgenic Metabolites from an Ascomycete, Corynascus setosus.
inferredcites →https://doi.org/10.7164/antibiotics.46.545openalex-snapshot
Fiscalins. New substance p inhibitors produced by the fungus Neosartorya fischeri. Taxonomy, fermentation, structures, and biological properties.
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.2021.112817zenodo-depositor-declared
Pyrazinopyrimidine alkaloids from a mangrove-derived fungus Aspergillus versicolor HDN11-84
inferred← citeshttps://doi.org/10.1002/adsc.202001235openalex-snapshot
A Stepwise Synthesis of Spiroindoline Compounds via Ring Opening of Aziridines and C−H Activation/Cyclization
inferred← citeshttps://doi.org/10.1002/adsc.202001535openalex-snapshot
Copper‐Catalyzed Three‐Component Cascade Reaction of Benzaldehyde with Benzylamine and Hydroxylamine or Aniline: Synthesis of 1,2,4‐Oxadiazoles and Quinazolines
inferred← citeshttps://doi.org/10.1002/ajoc.202200188openalex-snapshot
Enantioselective Synthesis of Chiral 3‐Alkynyl‐3‐Hydroxyindolin‐ 2‐Ones by Zn/bis(Sulfonamide)‐Diamine Catalyzed Asymmetric Addition of Alkynes to Isatins
inferred← citeshttps://doi.org/10.1002/cbdv.202200963openalex-snapshot
Chemical Constituents of the Deep‐Sea‐Derived Fungus Cladosporium oxysporum 170103 and Their Antibacterial Effects
inferred← citeshttps://doi.org/10.1002/cbdv.202200998openalex-snapshot
A Pair of Chromone Epimers and an Acetophenone Glucoside from the Mangrove Endophytic Fungus Mycosphaerella sp. L3A1
inferred← citeshttps://doi.org/10.1002/clen.201700238openalex-snapshot
Marine Fungi Against Aquaculture Pathogens and Induction of the Activity via Co‐Culture
inferred← citeshttps://doi.org/10.1002/ejoc.202001544openalex-snapshot
N‐Heterocyclic Carbene Catalyzed [3+2] Annulations of β‐Halocycloenals with Isatins and Mechanism Study
inferred← citeshttps://doi.org/10.1002/jhet.2609openalex-snapshot
One‐Pot Pseudo Five‐Component Synthesis of Some New bis(Quinazolinon‐4(1 H )‐one) Derivatives
inferred← citeshttps://doi.org/10.1002/med.21466openalex-snapshot
Biologically active quinoline and quinazoline alkaloids part I
inferred← citeshttps://doi.org/10.1002/med.21492openalex-snapshot
Biologically active quinoline and quinazoline alkaloids part II
inferred← citeshttps://doi.org/10.1002/ps.6709openalex-snapshot
Discovery of glyantrypine‐family alkaloids as novel antiviral and antiphytopathogenic‐fungus agents
inferred← citeshttps://doi.org/10.1007/978-3-030-85603-8_18openalex-snapshot
Fungal Biopharmaceuticals: Current Research, Production, and Potential Applications
inferred← citeshttps://doi.org/10.1007/978-3-031-63920-3_24-1openalex-snapshot
Chemistry and Biological Activities of Mangrove-Derived Fungi
inferred← citeshttps://doi.org/10.1007/978-3-031-91066-1_24openalex-snapshot
Chemistry and Biological Activities of Mangrove-Derived Fungi
inferred← citeshttps://doi.org/10.1007/978-3-032-23507-7_5openalex-snapshot
Immunomodulatory and Antiviral Fungal Metabolites
inferred← citeshttps://doi.org/10.1007/978-3-319-69075-9_3openalex-snapshot
Anti-infective Compounds from Marine Organisms
inferred← citeshttps://doi.org/10.1007/978-981-13-6198-2_9openalex-snapshot
Antitumor Activities of Secondary Metabolites from Marine Microbe Stress Responses to Virus Infection
inferred← citeshttps://doi.org/10.1007/978-981-99-9183-9_15openalex-snapshot
Natural Product-Based Anti-Viral Agents Against RNA Viruses: An Important Strategy for Pandemic Preparedness
inferred← citeshttps://doi.org/10.1007/s00253-014-5575-0openalex-snapshot
Antifungal and antiviral products of marine organisms
inferred← citeshttps://doi.org/10.1007/s00343-023-3084-7openalex-snapshot
Bioactive chemical constituents from the marine-derived fungus Cladosporium sp. DLT-5
inferred← citeshttps://doi.org/10.1007/s11030-019-09932-9openalex-snapshot
Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
inferred← citeshttps://doi.org/10.1007/s12272-014-0513-3openalex-snapshot
Penipyrols A–B and peniamidones A–D from the mangrove derived Penicillium solitum GWQ-143
inferred← citeshttps://doi.org/10.1007/s13225-025-00559-wopenalex-snapshot
Species diversity of Cladosporium in Citrus and the genetic mechanisms for C. cladosporioides complex to adapt broad host plants
inferred← citeshttps://doi.org/10.1007/s13659-022-00366-9openalex-snapshot
Alkaloids as potential antivirals. A comprehensive review
inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14960-1openalex-snapshot
Three Heterocyclic Rings Fused (5-5-5)
inferred← citeshttps://doi.org/10.1016/b978-0-12-822405-2.00023-2openalex-snapshot
Bioactive alkaloids
inferred← citeshttps://doi.org/10.1016/b978-0-323-91245-7.00017-1openalex-snapshot
Pathogens control using mangrove endophytic fungi
inferred← citeshttps://doi.org/10.1016/b978-0-443-13263-6.00012-2openalex-snapshot
Alkaloids from mangrove fungi: Applications and market potential
inferred← citeshttps://doi.org/10.1016/b978-0-443-18866-4.00009-2openalex-snapshot
Antiviral history and viral targets for antiviral therapy
inferred← citeshttps://doi.org/10.1016/b978-0-443-18870-1.00017-2openalex-snapshot
Alkaloids of forest fungi: diversity and therapeutic applications
inferred← citeshttps://doi.org/10.1016/b978-0-443-19049-0.00021-9openalex-snapshot
Fungal metabolites and their importance in pharmaceutical industry
inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105375openalex-snapshot
Biotransformations of anthranilic acid and phthalimide to potent antihyperlipidemic alkaloids by the marine-derived fungus Scedosporium apiospermum F41-1
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106482openalex-snapshot
Indoloquinazoline alkaloids with cardiomyocyte protective activity against cold ischemic injury from Aspergillus clavatonanicus
inferred← citeshttps://doi.org/10.1016/j.bioorg.2023.106873openalex-snapshot
Indoloquinazoline alkaloids suppress angiogenesis and inhibit metastasis of melanoma cells
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.06.072openalex-snapshot
Lipid-lowering polyketides from a soft coral-derived fungus Cladosporium sp. TZP29
inferred← citeshttps://doi.org/10.1016/j.bmcl.2018.03.036openalex-snapshot
One-pot, multicomponent synthesis of 2,3-disubstituted quinazolin-ones with potent and selective activity against Toxoplasma gondii
inferred← citeshttps://doi.org/10.1016/j.bse.2023.104741openalex-snapshot
Secondary metabolites from the endophytic fungus Cladosporium sp. ZLM-6
inferred← citeshttps://doi.org/10.1016/j.crbiot.2020.09.001openalex-snapshot
Insights about clinically approved and Preclinically investigated marine natural products
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.02.005openalex-snapshot
Recent advances in the structural library of functionalized quinazoline and quinazolinone scaffolds: Synthetic approaches and multifarious applications
inferred← citeshttps://doi.org/10.1016/j.ejmech.2014.10.065openalex-snapshot
A review on recent developments of indole-containing antiviral agents
inferred← citeshttps://doi.org/10.1016/j.ejmech.2022.114117openalex-snapshot
Natural products from mangrove sediments-derived microbes: Structural diversity, bioactivities, biosynthesis, and total synthesis
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.115726openalex-snapshot
Natural products as potential lead compounds to develop new antiviral drugs over the past decade
inferred← citeshttps://doi.org/10.1016/j.ejmech.2023.116081openalex-snapshot
The potential of marine-derived piperazine alkaloids: Sources, structures and bioactivities
inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104357openalex-snapshot
4-Hydroxy-pyran-2-one and 3-hydroxy-N-methyl-2-oxindole derivatives of Salinispora arenicola from Brazilian marine sediments
inferred← citeshttps://doi.org/10.1016/j.jiac.2024.06.013openalex-snapshot
Sorbicillinoid HSL-2 inhibits the infection of influenza A virus via interaction with the PPAR-γ/NF-κB pathway
inferred← citeshttps://doi.org/10.1016/j.phytochem.2016.09.008openalex-snapshot
Chevalone C analogues and globoscinic acid derivatives from the fungus Neosartorya spinosa KKU-1NK1
inferred← citeshttps://doi.org/10.1016/j.phytochem.2020.112374openalex-snapshot
Structurally diverse and bioactive alkaloids from an insect-derived fungus Neosartorya fischeri
inferred← citeshttps://doi.org/10.1016/j.sajb.2020.01.006openalex-snapshot
Anti-infectives from mangrove endophytic fungi
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2020.143539openalex-snapshot
Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents
inferred← citeshttps://doi.org/10.1016/j.tchem.2024.100062openalex-snapshot
Diversity oriented total synthesis (DOTS) of pyridoquinazolinone alkaloids and their analogues
inferred← citeshttps://doi.org/10.1016/j.tet.2014.11.063openalex-snapshot
New glucosidated pyrazinoquinazoline indole alkaloids from fungus Aspergillus fumigatus derived of a jellyfish
inferred← citeshttps://doi.org/10.1016/j.tet.2014.12.006openalex-snapshot
New efficient synthesis of 1H-pyrimido[2,1-b]quinazoline-2,6-diones via a tandem aza-Wittig/nucleophilic addition/intramolecular cyclization/isomerization reaction starting from the Baylis–Hillman adducts
inferred← citeshttps://doi.org/10.1016/j.tet.2016.07.080openalex-snapshot
Campyridones A–D, pyridone alkaloids from a mangrove endophytic fungus Campylocarpon sp. HDN13-307
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.156289openalex-snapshot
Indole-quinazoline alkaloids with anti-inflammatory activity from fungus Aspergillus clavatonanicus
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c06430openalex-snapshot
Mediterranean Seaweeds: Bridging Chemistry Knowledge, Microbial Community Profiling, Therapeutic, Nutraceutical, and Industrial Applications
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.1c00098openalex-snapshot
17-Hydroxybrevianamide N and Its N1-Methyl Derivative, Quinazolinones from a Soft-Coral-Derived Aspergillus sp. Fungus: 13S Enantiomers as the True Natural Products
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c01157openalex-snapshot
Absolute Configuration of 12S-Deoxynortryptoquivaline from Ascidian-Derived Fungus Aspergillus clavatus Determined by Anisotropic NMR and Chiroptical Spectroscopy
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c01575openalex-snapshot
Discovery of an Indole-Quinazoline Alkaloid as an Anti-kidney Fibrotic Agent from the Marine-Derived Aspergillus clavatonanicus SCSIO 41444
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.7b00644openalex-snapshot
Saroclides A and B, Cyclic Depsipeptides from the Mangrove-Derived Fungus Sarocladium kiliense HDN11-112
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b01096openalex-snapshot
Potential Antidiabetic Fumiquinazoline Alkaloids from the Marine-Derived Fungus Scedosporium apiospermum F41‑1
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00476openalex-snapshot
Catalyst-Free Annulation of Acylethynylpyrroles with 1-Pyrrolines: A Straightforward Access to Tetrahydrodipyrrolo[1,2-a:1′,2′-c]imidazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.2c02638openalex-snapshot
t-BuOK-Catalyzed Regio- and Stereoselective Intramolecular Hydroamination Reaction Leading to Phthalazinoquinazolinone Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01349openalex-snapshot
Cobalt-Catalyzed Enantioselective Arylation of Isatin Derivatives with Arylboronic Acids
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02023openalex-snapshot
Synthesis of Spirooxindole-γ-Lactones via Engaging Oxindole-Templated Azaoxyallyl Cation with 2-Naphthols
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02268openalex-snapshot
Nonenzymatic Self-Assembly Access to Diverse ortho-Quinone Methide-Based Pseudonatural Products
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02964openalex-snapshot
Neosartoryadins A and B, Fumiquinazoline Alkaloids from a Mangrove-Derived Fungus Neosartorya udagawae HDN13-313
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01374openalex-snapshot
A Tandem Oxidative Annulation Strategy for the Synthesis of Tetracyclic 3-Spirooxindole Benzofuranones
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02238openalex-snapshot
Amino Acid-Directed Strategy for Inducing the Marine-Derived Fungus Scedosporium apiospermum F41–1 to Maximize Alkaloid Diversity
inferred← citeshttps://doi.org/10.1021/np4005757openalex-snapshot
Meroterpenoids with Diverse Ring Systems from the Sponge-Associated FungusAlternariasp. JJY-32
inferred← citeshttps://doi.org/10.1021/np500458aopenalex-snapshot
Eleganketal A, a Highly Oxygenated Dibenzospiroketal from the Marine-Derived FungusSpicaria elegansKLA03
inferred← citeshttps://doi.org/10.1021/np500586ropenalex-snapshot
Penicitols A–C and Penixanacid A from the Mangrove-Derived Penicillium chrysogenum HDN11-24
inferred← citeshttps://doi.org/10.1038/s41598-025-90304-9openalex-snapshot
Exploring the antitrypanosomal potential of rosemary root endophytic fungi with metabolomic profiling and molecular docking insights
inferred← citeshttps://doi.org/10.1039/c4ra11756eopenalex-snapshot
Bioactive natural products derived from mangrove-associated microbes
inferred← citeshttps://doi.org/10.1039/c5ob01379hopenalex-snapshot
Recent developments in the chemistry of quinazolinone alkaloids
inferred← citeshttps://doi.org/10.1039/c8np00043copenalex-snapshot
Chemistry of the fumiquinazolines and structurally related alkaloids
inferred← citeshttps://doi.org/10.1039/c8qo00670aopenalex-snapshot
Palladium-catalyzed oxidative CC bond cleavage with molecular oxygen: one-pot synthesis of quinazolinones from 2-amino benzamides and alkenes
inferred← citeshttps://doi.org/10.1039/c8ra06854bopenalex-snapshot
Versiquinazolines L–Q, new polycyclic alkaloids from the marine-derived fungus Aspergillus versicolor
inferred← citeshttps://doi.org/10.1039/c9np00013eopenalex-snapshot
Extracting value: mechanistic insights into the formation of natural product artifacts – case studies in marine natural products
inferred← citeshttps://doi.org/10.1039/d0ob01099eopenalex-snapshot
The chemical gymnastics of enterocin: evidence for stereodivergence in Nature
inferred← citeshttps://doi.org/10.1039/d0ra05319hopenalex-snapshot
New marine-derived indolymethyl pyrazinoquinazoline alkaloids with promising antimicrobial profiles
inferred← citeshttps://doi.org/10.1039/d1np00041aopenalex-snapshot
Secondary metabolites from mangrove-associated fungi: source, chemistry and bioactivities
inferred← citeshttps://doi.org/10.1039/d2cc00167eopenalex-snapshot
Synthesis of polycyclic aminal heterocycles via decarboxylative cyclisation of dipeptide derivatives
inferred← citeshttps://doi.org/10.1039/d3nj05049aopenalex-snapshot
Eco-friendly, in-water, and catalyst-free assembly of acylethenylpyrroloimidazoindoles from 3 H -indoles and acylpyrrolylacetylenes
inferred← citeshttps://doi.org/10.1039/d3ra02217jopenalex-snapshot
2-Oxindole and related heterocycles: synthetic methodologies for their natural products and related derivatives
inferred← citeshttps://doi.org/10.1039/d3ra04012gopenalex-snapshot
Cladoxanthones C–G, xanthone derivatives from Cladosporium sp.
inferred← citeshttps://doi.org/10.1039/d4ob01795aopenalex-snapshot
Quinazolinone nitriles and related metabolites from the deep-sea-derived fungus Penicillium viridicatum MCCC 3A00265
inferred← citeshttps://doi.org/10.1039/d5ob00672dopenalex-snapshot
Iodine-promoted oxidative cross-coupling for the synthesis of ( E )-2-(3-oxo-3-phenylprop-1-en-1-yl)-3-phenylquinazolin-4(3 H )-one via C–H activation: development of synthetic TLX agonists
inferred← citeshttps://doi.org/10.1039/d6ra05034dopenalex-snapshot
Ultrasonic and mechanochemical strategies for the synthesis of oxindole scaffolds mediated by hypervalent iodine( iii ) reagents
inferred← citeshttps://doi.org/10.1055/a-2376-6463openalex-snapshot
Recent Advances in Asymmetric Addition Reactions to Isatins
inferred← citeshttps://doi.org/10.1080/07391102.2020.1776639openalex-snapshot
Virtual screening-driven drug discovery of SARS-CoV2 enzyme inhibitors targeting viral attachment, replication, post-translational modification and host immunity evasion infection mechanisms
inferred← citeshttps://doi.org/10.1080/10286020.2024.2362384openalex-snapshot
Secondary metabolites from the fungus Cladosporium xylophilum
inferred← citeshttps://doi.org/10.1080/14786419.2018.1431634openalex-snapshot
Two new secondary metabolites from a mangrove-derived fungus Cladosporium sp. JJM22
inferred← citeshttps://doi.org/10.1080/14786419.2018.1556266openalex-snapshot
New citrinin derivatives from the deep-sea-derived fungus Cladosporium sp. SCSIO z015
inferred← citeshttps://doi.org/10.1080/14786419.2019.1641807openalex-snapshot
Cladosporine A, a new indole diterpenoid alkaloid with antimicrobial activities from Cladosporium sp.
inferred← citeshttps://doi.org/10.1080/14786419.2022.2137798openalex-snapshot
Chemical constituents of Aspergillus udagawae isolated from the soil of the Xingren coal areas and their antibacterial activities
inferred← citeshttps://doi.org/10.1080/14786419.2024.2444571openalex-snapshot
Antibacterial compounds from an endophytic fungus Cladosporium colombiae GTJ67
inferred← citeshttps://doi.org/10.1080/26895293.2025.2603824openalex-snapshot
Endophyte-derived metabolites mediate immunomodulation in Brassica rapa subsp rapa L.
inferred← citeshttps://doi.org/10.1111/cbdd.12736openalex-snapshot
Synthesis, Polymorphism, and Insecticidal Activity of Methyl 4‐(4‐chlorophenyl)‐8‐iodo‐2‐methyl‐6‐oxo‐1,6‐dihydro‐4H‐pyrimido[2,1‐b]quinazoline‐3‐Carboxylate Against Anopheles arabiensis Mosquito
inferred← citeshttps://doi.org/10.1155/2014/375423openalex-snapshot
Indole Alkaloids from Marine Sources as Potential Leads against Infectious Diseases
inferred← citeshttps://doi.org/10.1155/2021/3613268openalex-snapshot
Quinoline and Quinazoline Alkaloids against COVID-19: An In Silico Multitarget Approach
inferred← citeshttps://doi.org/10.1177/2040206617705500openalex-snapshot
Potential of small-molecule fungal metabolites in antiviral chemotherapy
inferred← citeshttps://doi.org/10.1371/journal.pone.0144394openalex-snapshot
Exploring the Antibacterial and Antifungal Potential of Jellyfish-Associated Marine Fungi by Cultivation-Dependent Approaches
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2954577/v1openalex-snapshot
Metabolic composition of endophytes contributed to the effect of Brassica rapa L. in improving immunity
inferred← citeshttps://doi.org/10.2147/dddt.s299120openalex-snapshot
Progress of Plant Medicine Derived Extracts and Alkaloids on Modulating Viral Infections and Inflammation
inferred← citeshttps://doi.org/10.2174/0929867327666201026150105openalex-snapshot
Marine Natural Products as a Source of Drug Leads against Respiratory Viruses: Structural and Bioactive Diversity
inferred← citeshttps://doi.org/10.2174/1389557520666200925142514openalex-snapshot
An Updated Review of Secondary Metabolites from Marine Fungi
inferred← citeshttps://doi.org/10.2174/1389557521666210831152511openalex-snapshot
The Effect of Plant Metabolites on Coronaviruses: A Comprehensive Review Focusing on their IC50 Values and Molecular Docking Scores
inferred← citeshttps://doi.org/10.2183/pjab.101.017openalex-snapshot
Mechanism of puberulic acid contamination in red yeast rice tablets that caused a serious food poisoning outbreak in Japan
inferred← citeshttps://doi.org/10.26434/chemrxiv.12170424openalex-snapshot
Not One, But Five: Virtual Screening-Driven Drug Discovery of SARS-CoV2 Enzyme Inhibitors Targeting Viral Attachment, Replication and Post-Translational Infection Mechanisms
inferred← citeshttps://doi.org/10.26434/chemrxiv.12170424.v1openalex-snapshot
Not One, But Five: Virtual Screening-Driven Drug Discovery of SARS-CoV2 Enzyme Inhibitors Targeting Viral Attachment, Replication and Post-Translational Infection Mechanisms
inferred← citeshttps://doi.org/10.29267/mxjb.2021.6.1.165openalex-snapshot
Bioactive compounds from fungi with antiviral activities: Mechanism of action and biosynthetic pathways
inferred← citeshttps://doi.org/10.32604/biocell.2022.019301openalex-snapshot
Secondary antiviral metabolites from fungi with special reference to coronaviruses
inferred← citeshttps://doi.org/10.32604/or.2023.030266openalex-snapshot
Deoxynortryptoquivaline: A unique antiprostate cancer agent
inferred← citeshttps://doi.org/10.3389/fchem.2021.773703openalex-snapshot
Metabolites From the Mangrove-Derived Fungus Cladosporium sp. HNWSW-1
inferred← citeshttps://doi.org/10.3389/fchem.2022.991026openalex-snapshot
Recent advances and prospects in the organocatalytic synthesis of quinazolinones
inferred← citeshttps://doi.org/10.3389/fmicb.2015.01485openalex-snapshot
Extrolites of Aspergillus fumigatus and Other Pathogenic Species in Aspergillus Section Fumigati
inferred← citeshttps://doi.org/10.3389/fmicb.2018.02325openalex-snapshot
Antiviral Agents From Fungi: Diversity, Mechanisms and Potential Applications
inferred← citeshttps://doi.org/10.3389/fmicb.2021.680879openalex-snapshot
Three New Quinazoline-Containing Indole Alkaloids From the Marine-Derived Fungus Aspergillus sp. HNMF114
inferred← citeshttps://doi.org/10.3389/fmolb.2021.732256openalex-snapshot
Microbial Metabolites: The Emerging Hotspot of Antiviral Compounds as Potential Candidates to Avert Viral Pandemic Alike COVID-19
inferred← citeshttps://doi.org/10.3390/agronomy12081840openalex-snapshot
Design, Synthesis, Mode of Action and Herbicidal Evaluation of Quinazolin-4(3H)-one Derivatives Based on Aryloxyphenoxypropionate Motif
inferred← citeshttps://doi.org/10.3390/antibiotics12050922openalex-snapshot
Effect of Indole-Containing Pyrazino[2,1-b]quinazoline-3,6-diones in the Virulence of Resistant Bacteria
inferred← citeshttps://doi.org/10.3390/ijms24043404openalex-snapshot
Contributing to Biochemistry and Optoelectronics: Pyrrolo[1′,2′:2,3]imidazo[1,5-a]indoles and Cyclohepta[4,5]pyrrolo[1,2-c]pyrrolo[1,2-a]imidazoles via [3+2] Annulation of Acylethynylcycloalka[b]pyrroles with Δ1-Pyrrolines
inferred← citeshttps://doi.org/10.3390/ijms25031652openalex-snapshot
The Genus Cladosporium: A Prospective Producer of Natural Products
inferred← citeshttps://doi.org/10.3390/md13074520openalex-snapshot
Potential Antiviral Agents from Marine Fungi: An Overview
inferred← citeshttps://doi.org/10.3390/md13106489openalex-snapshot
Alkaloids with Cardiovascular Effects from the Marine-Derived Fungus Penicillium expansum Y32
inferred← citeshttps://doi.org/10.3390/md14070132openalex-snapshot
Chamigrane Sesquiterpenes from a Basidiomycetous Endophytic Fungus XG8D Associated with Thai Mangrove Xylocarpus granatum
inferred← citeshttps://doi.org/10.3390/md15090273openalex-snapshot
Marine Pharmacology in 2012–2013: Marine Compounds with Antibacterial, Antidiabetic, Antifungal, Anti-Inflammatory, Antiprotozoal, Antituberculosis, and Antiviral Activities; Affecting the Immune and Nervous Systems, and Other Miscellaneous Mechanisms of Action
inferred← citeshttps://doi.org/10.3390/md16080261openalex-snapshot
Antitumor Activity of Quinazolinone Alkaloids Inspired by Marine Natural Products
inferred← citeshttps://doi.org/10.3390/md17050296openalex-snapshot
Polyketides from the Mangrove-Derived Endophytic Fungus Cladosporium cladosporioides
inferred← citeshttps://doi.org/10.3390/md19090492openalex-snapshot
Secondary Metabolites with α-Glucosidase Inhibitory Activity from Mangrove Endophytic Fungus Talaromyces sp. CY-3
inferred← citeshttps://doi.org/10.3390/md19110645openalex-snapshot
Untapped Potential of Marine-Associated Cladosporium Species: An Overview on Secondary Metabolites, Biotechnological Relevance, and Biological Activities
inferred← citeshttps://doi.org/10.3390/md20050302openalex-snapshot
Discovery of Anti-MRSA Secondary Metabolites from a Marine-Derived Fungus Aspergillus fumigatus
inferred← citeshttps://doi.org/10.3390/md22050214openalex-snapshot
Bioactive Alkaloids from the Mangrove-Derived Fungus Nigrospora oryzae SYSU-MS0024
inferred← citeshttps://doi.org/10.3390/metabo11020107openalex-snapshot
Chemical Elicitors Induce Rare Bioactive Secondary Metabolites in Deep-Sea Bacteria under Laboratory Conditions
inferred← citeshttps://doi.org/10.3390/microorganisms9122481openalex-snapshot
Structure-Function Characteristics of SARS-CoV-2 Proteases and Their Potential Inhibitors from Microbial Sources
inferred← citeshttps://doi.org/10.3390/molecules27134305openalex-snapshot
Microbial Natural Products with Antiviral Activities, Including Anti-SARS-CoV-2: A Review
inferred← citeshttps://doi.org/10.3390/molecules29030649openalex-snapshot
Chemical Constituents and Bioactivities of the Plant-Derived Fungus Aspergillus fumigatus
inferred← citeshttps://doi.org/10.3390/molecules29092112openalex-snapshot
A New Quinazolinone Alkaloid along with Known Compounds with Seed-Germination-Promoting Activity from Rhodiola tibetica Endophytic Fungus Penicillium sp. HJT-A-6
inferred← citeshttps://doi.org/10.3390/toxins11110656openalex-snapshot
The Biological Activity of Natural Alkaloids against Herbivores, Cancerous Cells and Pathogens
inferred← citeshttps://doi.org/10.3390/v14112452openalex-snapshot
Antiviral Potential of Natural Resources against Influenza Virus Infections
inferred← citeshttps://doi.org/10.36348/sjpm.2022.v07i01.002openalex-snapshot
Endophytic, Non-endophytic Fungal Alkaloids and its Applications
inferred← citeshttps://doi.org/10.58257/ijprems32588openalex-snapshot
Alkaloids As Potential Antiviral : A Comprehensive Review
inferred← citeshttps://doi.org/10.70675/bce74b88z823az456cz89dbzb52b95589821openalex-snapshot
Total synthesis of cyclotripeptidic natural products in the aurantiomide series, under oxidative functionnalisation conditions
inferred← citeshttps://doi.org/10.70675/e743d4abz5b6az450cz8a64zb705408734eaopenalex-snapshot
Allylboration énantiosélective et organocatalysée d’alpha-céto-amides : applications à la synthèse d’un produit naturel et de composés spiraniques
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
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