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Cytotoxic and Antibacterial Eremophilane Sesquiterpenes from the Marine-Derived Fungus Cochliobolus lunatus SCSIO41401

https://doi.org/10.1021/acs.jnatprod.8b00015

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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/hlca.19890720304openalex-snapshot

Novel Trinor‐eremophilanes (Dendryphiellin B, C, and D), Eremophilanes (Dendryphiellin E, F, and G), and Branched C9‐Carboxylic Acids (Dendryphiellic Acid A and B) from the Marine Deuteromycete Dendryphiella salina (S UTHERLAND ) P UGH et N ICOT

inferredcites →https://doi.org/10.1002/jcc.540161202openalex-snapshot

Remarks on the use of the apparent surface charges (ASC) methods in solvation problems: Iterative versus matrix‐inversion procedures and the renormalization of the apparent charges

inferredcites →https://doi.org/10.1007/bfb0016643openalex-snapshot

Density functional theory of time-dependent phenomena

inferredcites →https://doi.org/10.1007/s11101-010-9178-9openalex-snapshot

Bioactive natural products from marine sponges and fungal endophytes

inferredcites →https://doi.org/10.1016/j.bmcl.2015.12.005openalex-snapshot

Aspernigrins with anti-HIV-1 activities from the marine-derived fungus Aspergillus niger SCSIO Jcsw6F30

inferredcites →https://doi.org/10.1016/j.phytochem.2016.03.005openalex-snapshot

Eremophilane sesquiterpenes from Hawaiian endophytic fungus Chaetoconis sp. FT087

inferredcites →https://doi.org/10.1016/s0968-0896(98)00088-1openalex-snapshot

KM-01, a brassinolide inhibitor, its production, isolation and structure from two fungi Drechslera avenae and Pycnoporus coccineus

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00810openalex-snapshot

Ochracenes A–I, Humulane-Derived Sesquiterpenoids from the Antarctic Fungus Aspergillus ochraceopetaliformis

inferredcites →https://doi.org/10.1021/acs.jnatprod.6b00953openalex-snapshot

Complementarity of DFT Calculations, NMR Anisotropy, and ECD for the Configurational Analysis of Brevipolides K–O from Hyptis brevipes

inferredcites →https://doi.org/10.1021/acs.jnatprod.7b00698openalex-snapshot

Nitrobenzoyl Sesquiterpenoids with Cytotoxic Activities from a Marine-Derived Aspergillus ochraceus Fungus

inferredcites →https://doi.org/10.1021/np1005345openalex-snapshot

Stachylines A−D from the Sponge-Derived Fungus Stachylidium sp.

inferredcites →https://doi.org/10.1021/np5009224openalex-snapshot

Phytotoxic Eremophilane Sesquiterpenes from the Coprophilous FungusPenicilliumsp. G1-a14

inferredcites →https://doi.org/10.1021/np8004503openalex-snapshot

Phthalides from Pittosporum illicioides var. illicioides with Inhibitory Activity on Superoxide Generation and Elastase Release by Neutrophils

inferredcites →https://doi.org/10.1038/nprot.2008.141openalex-snapshot

A simple and reproducible 96-well plate-based method for the formation of fungal biofilms and its application to antifungal susceptibility testing

inferredcites →https://doi.org/10.1039/c3md00371jopenalex-snapshot

Cytotoxic and antiviral nitrobenzoyl sesquiterpenoids from the marine-derived fungus Aspergillus ochraceus Jcma1F17

inferredcites →https://doi.org/10.1039/p19830002185openalex-snapshot

Metabolites of the higher fungi. Part 21. 3-Methyl-3,4-dihydroisocoumarins and related compounds from the ascomycete family xylariaceae

inferredcites →https://doi.org/10.1080/14786419.2017.1399382openalex-snapshot

Dereplication and targeted isolation of bioactive sulphur compound from bacteria isolated from a hydrothermal field

inferredcites →https://doi.org/10.1515/znb-2016-0128openalex-snapshot

Purpureone, an antileishmanial ergochrome from the endophytic fungus Purpureocillium lilacinum

inferredcites →https://doi.org/10.3390/molecules21040473openalex-snapshot

Eremophilane Sesquiterpenes from a Deep Marine-Derived Fungus, Aspergillus sp. SCSIOW2, Cultivated in the Presence of Epigenetic Modifying Agents

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.2020.112642zenodo-depositor-declared

Trinor- and tetranor-eremophilane sesquiterpenoids with anti-neuroinflammatory activity from cultures of the fungus Septoria rudbeckiae

inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113294zenodo-depositor-declared

Aureoterrolides B‒M: Eremophilane-type sesquiterpenoids isolated from Aspergillus aureoterreus and their cytotoxicity

inferred← citeshttps://doi.org/10.1002/adsc.201901115openalex-snapshot

Electrochemical Difunctionalization of Olefines: Access to Selenomethyl‐Substituted Cyclic Ethers or Lactones

inferred← citeshttps://doi.org/10.1002/cbdv.202100663openalex-snapshot

Azaphilones and Meroterpenoids from the Soft Coral‐Derived Fungus Penicillium glabrum glmu003

inferred← citeshttps://doi.org/10.1002/cbdv.202200513openalex-snapshot

Marine Based Natural Products: Exploring the Recent Developments in the Identification of Antimicrobial Agents

inferred← citeshttps://doi.org/10.1002/slct.202202004openalex-snapshot

An Overview of Natural and Synthetic Phthalides Involved in Cancer Studies: Past, Present, and Future

inferred← citeshttps://doi.org/10.1007/978-981-97-9634-2_1openalex-snapshot

Natural Products for Antibacterial Infections in Current Scenario

inferred← citeshttps://doi.org/10.1007/s00253-022-11939-6openalex-snapshot

Marine fungal metabolites as a source of drug leads against aquatic pathogens

inferred← citeshttps://doi.org/10.1007/s10600-021-03366-2openalex-snapshot

Chemical Constituents of the Endophytic Fungus Bipolaris maydis Derived from the Kandelia candel

inferred← citeshttps://doi.org/10.1007/s11101-020-09705-5openalex-snapshot

Antimicrobial compounds from marine fungi

inferred← citeshttps://doi.org/10.1007/s12272-024-01500-6openalex-snapshot

Antibacterial properties of natural products from marine fungi reported between 2012 and 2023: a review

inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103922openalex-snapshot

Recent progress of antibacterial natural products: Future antibiotics candidates

inferred← citeshttps://doi.org/10.1016/j.bioorg.2021.105247openalex-snapshot

Eremophilane sesquiterpenoids from the whole plant of Parasenecio albus with immunosuppressive activity

inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112957openalex-snapshot

Chemistry, biosynthesis and biological activity of terpenoids and meroterpenoids in bacteria and fungi isolated from different marine habitats

inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105223openalex-snapshot

Recent advances in natural phthalides: Distribution, chemistry, and biological activities

inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145747openalex-snapshot

Phthalides from Ligusticum chuanxiong Hort. protect PC12 cells against OGD/R-induced injury

inferred← citeshttps://doi.org/10.1016/j.phrs.2022.106391openalex-snapshot

Marine pharmacology in 2018: 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/10.1016/j.phytochem.2025.114677openalex-snapshot

Acroeremophilanes A–I, eremophilane-type sesquiterpenoids from the Sinomenium acutum-derived symbiotic fungus Acrocalymma cycadis

inferred← citeshttps://doi.org/10.1016/j.tet.2023.133297openalex-snapshot

Eremophilane sesquiterpenoids from the endophytic fungus Curvularia lunata BCC76963

inferred← citeshttps://doi.org/10.1016/s1875-5364(19)30017-2openalex-snapshot

Peptides and polyketides isolated from the marine sponge-derived fungus Aspergillus terreus SCSIO 41008

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00050openalex-snapshot

Ene-yne Hydroquinones from a Marine-derived Strain of the Fungus Pestalotiopsis neglecta with Effects on Liver X Receptor Alpha

inferred← citeshttps://doi.org/10.1021/acs.jnatprod.8b00656openalex-snapshot

Spirostaphylotrichin X from a Marine-Derived Fungus as an Anti-influenza Agent Targeting RNA Polymerase PB2

inferred← citeshttps://doi.org/10.1038/s41429-020-00386-yopenalex-snapshot

Structurally diverse polyketides and phenylspirodrimanes from the soft coral-associated fungus Stachybotrys chartarum SCSIO41201

inferred← citeshttps://doi.org/10.1039/c9np00069kopenalex-snapshot

Marine natural products

inferred← citeshttps://doi.org/10.1039/c9ob01595gopenalex-snapshot

Sorbicillfurans A and B, two novel sorbicillinoid adducts from the fungus Penicillium citrinum SCSIO41402

inferred← citeshttps://doi.org/10.1039/d0ob00303dopenalex-snapshot

Acid–base-sensitive allylic oxidation of 2-allylbenzoic acids to form phthalides

inferred← citeshttps://doi.org/10.1039/d1ra00788bopenalex-snapshot

New protein tyrosine phosphatase inhibitors from fungus Aspergillus gorakhpurensis F07ZB1707

inferred← citeshttps://doi.org/10.1080/14786419.2019.1636237openalex-snapshot

Two new phthalide derivatives from the endophytic fungus Penicillium vulpinum isolated from Sophora tonkinensis

inferred← citeshttps://doi.org/10.1080/14786419.2020.1765339openalex-snapshot

Maydisone, a novel oxime polyketide from the cultures of Bipolaris maydis

inferred← citeshttps://doi.org/10.1134/s1068162020060023openalex-snapshot

Antibiotics from Extremophilic Micromycetes

inferred← citeshttps://doi.org/10.1177/1934578x221109527openalex-snapshot

Cumulative Data of 1 H and 13 C NMR Signals and Specific Rotations of Eremophilane Sesquiterpenoids. 1. Bicyclic Eremophilanes (1)

inferred← citeshttps://doi.org/10.1177/1934578x221141172openalex-snapshot

Cumulative Data of 1 H and 13 C NMR Signals and Specific Rotations of Eremophilane Sesquiterpenoids. 2. Bicyclic Eremophilanes (2)

inferred← citeshttps://doi.org/10.14692/jfi.18.2.53-65openalex-snapshot

Screening of Marine Fungi as Biological Control Agent of Colletotrichum acutatum on Chili

inferred← citeshttps://doi.org/10.31579/2693-7247/031openalex-snapshot

Cochliobolus, Drechslera, Bipolaris, Curvularia different nomenclature for one potent fungus

inferred← citeshttps://doi.org/10.3390/cimb48090902openalex-snapshot

AI-Powered Marine Drug Discovery: A Putative Dual c-Met/VEGFR2 Lead Candidate for Hepatocellular Carcinoma via Deep Learning and Multiscale Simulation

inferred← citeshttps://doi.org/10.3390/md16080279openalex-snapshot

Current Screening Methodologies in Drug Discovery for Selected Human Diseases

inferred← citeshttps://doi.org/10.3390/md16090335openalex-snapshot

Cytotoxic Tetrahydroxanthone Dimers from the Mangrove-Associated Fungus Aspergillus versicolor HDN1009

inferred← citeshttps://doi.org/10.3390/md17060339openalex-snapshot

Bioactive Compounds Isolated from Marine-Derived Microbes in China: 2009–2018

inferred← citeshttps://doi.org/10.3390/md18060321openalex-snapshot

A Review of Terpenes from Marine-Derived Fungi: 2015–2019

inferred← citeshttps://doi.org/10.3390/md18110547openalex-snapshot

Lipopeptide Epimers and a Phthalide Glycerol Ether with AChE Inhibitory Activities from the Marine-Derived Fungus Cochliobolus Lunatus SCSIO41401

inferred← citeshttps://doi.org/10.3390/md18120597openalex-snapshot

Isolation and Characterization of New Anti-Inflammatory and Antioxidant Components from Deep Marine-Derived Fungus Myrothecium sp. Bzo-l062

inferred← citeshttps://doi.org/10.3390/md20110712openalex-snapshot

Eremophilane-Type Sesquiterpenes from a Marine-Derived Fungus Penicillium Copticola with Antitumor and Neuroprotective Activities

inferred← citeshttps://doi.org/10.3390/md21060327openalex-snapshot

Bioactive Polyketides and Benzene Derivatives from Two Mangrove Sediment-Derived Fungi in the Beibu Gulf

inferred← citeshttps://doi.org/10.3390/md22070288openalex-snapshot

Effects of Marine Natural Products on Liver Diseases

inferred← citeshttps://doi.org/10.3390/molecules25112485openalex-snapshot

Natural Nitrogenous Sesquiterpenoids and Their Bioactivity: A Review

inferred← citeshttps://doi.org/10.3390/molecules30204068openalex-snapshot

Eremophilane-Type Sesquiterpenoids from Fungus Aspergillus aurantiobrunneus

inferred← citeshttps://doi.org/10.4018/979-8-3693-6972-2.ch014openalex-snapshot

Marine World of Terpenes Targeting Specific Cancers

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