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Ophiobolins from the Mangrove Fungus Aspergillus ustus
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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.201000283openalex-snapshot
Ophiobolin Sesterterpenoids and Pyrrolidine Alkaloids from the Sponge‐Derived Fungus Aspergillus ustus
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/10.1016/0968-0896(96)00036-3openalex-snapshot
Ophiobolin M and analogues, noncompetitive inhibitors of ivermectin binding with nematocidal activity
inferredcites →https://doi.org/10.1016/j.bmcl.2013.04.034openalex-snapshot
3-Anhydro-6-hydroxy-ophiobolin A, a new sesterterpene inhibiting the growth of methicillin-resistant Staphylococcus aureus and inducing the cell death by apoptosis on K562, from the phytopathogenic fungus Bipolaris oryzae
inferredcites →https://doi.org/10.1016/j.fitote.2013.08.002openalex-snapshot
Ophiobolins P–T, five new cytotoxic and antibacterial sesterterpenes from the endolichenic fungus Ulocladium sp.
inferredcites →https://doi.org/10.1016/j.phytochem.2006.07.016openalex-snapshot
Ophiobolin E and 8-epi-ophiobolin J produced by Drechslera gigantea, a potential mycoherbicide of weedy grasses
inferredcites →https://doi.org/10.1016/j.tet.2004.05.021openalex-snapshot
Cytotoxic sesterterpenes, 6-epi-ophiobolin G and 6-epi-ophiobolin N, from marine derived fungus Emericella variecolor GF10
inferredcites →https://doi.org/10.1016/s0040-4020(01)96148-4openalex-snapshot
Structure and conformation of ophiobolin K and 6- epiophiobolin K from Aspergillus ustus as a nematocidal agent.
inferredcites →https://doi.org/10.1016/s0040-4039(00)72395-1openalex-snapshot
The constitution of cochliobolin
inferredcites →https://doi.org/10.1016/s0040-4039(00)72403-8openalex-snapshot
The structure of zizannin-A and -B, C25-terpenoids isolated from
inferredcites →https://doi.org/10.1016/s0040-4039(01)85110-8openalex-snapshot
A new natural ophiobolin
inferredcites →https://doi.org/10.1016/s0040-4039(01)89701-xopenalex-snapshot
The structure of cephalonic acid, a pentaprenyl terpenoid
inferredcites →https://doi.org/10.1016/s0040-4039(01)99159-2openalex-snapshot
The isolation of an acyclic C25-isoprenoid alcohol, geranylnerolidol, and a new ophiobolin
inferredcites →https://doi.org/10.1016/s0040-4039(01)99717-5openalex-snapshot
Isolation and constitution of cochliobolin b
inferredcites →https://doi.org/10.1021/ja00949a061openalex-snapshot
The Structure of Ophiobolin, a C25 Terpenoid Having a Novel Skeleton
inferredcites →https://doi.org/10.1021/jf00124a019openalex-snapshot
Ophiobolins G and H: new fungal metabolites from a novel source, Aspergillus ustus
inferredcites →https://doi.org/10.1021/jf052843lopenalex-snapshot
Herbicidal Potential of Ophiobolins Produced by Drechslera gigantea
inferredcites →https://doi.org/10.1021/jo00245a008openalex-snapshot
Some new phytotoxic ophiobolins produced by Drechslera oryzae
inferredcites →https://doi.org/10.1021/np400304qopenalex-snapshot
Indole-Diterpenoids with Anti-H1N1 Activity from the Aciduric Fungus Penicillium camemberti OUCMDZ-1492
inferredcites →https://doi.org/10.1021/np400802dopenalex-snapshot
Thiodiketopiperazines from the Marine-Derived Fungus Phoma sp. OUCMDZ-1847
inferredcites →https://doi.org/10.1021/np50115a009openalex-snapshot
Microbial Metabolites of Ophiobolin A and Antimicrobial Evaluation of Ophiobolins
inferredcites →https://doi.org/10.1021/np900268zopenalex-snapshot
Sesquiterpenoids and Benzofuranoids from the Marine-Derived Fungus Aspergillus ustus 094102
inferredcites →https://doi.org/10.1021/np980462eopenalex-snapshot
Characterization of 6-epi-3-Anhydroophiobolin B from Cochliobolus heterostrophus
inferredcites →https://doi.org/10.1021/ol103164nopenalex-snapshot
New Quinazolinone Alkaloids within Rare Amino Acid Residue from Coral-Associated Fungus, Aspergillus versicolor LCJ-5-4
inferredcites →https://doi.org/10.1038/ja.2013.135openalex-snapshot
New rubrolides from the marine-derived fungus Aspergillus terreus OUCMDZ-1925
inferredcites →https://doi.org/10.1038/srep20004openalex-snapshot
New α-glucosidase inhibitors from marine algae-derived Streptomyces sp. OUCMDZ-3434
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/b515476fopenalex-snapshot
Application of electronic circular dichroism in configurational and conformational analysis of organic compounds
inferredcites →https://doi.org/10.1039/b607254mopenalex-snapshot
Marine natural products of fungal origin
inferredcites →https://doi.org/10.1039/c2ra22701kopenalex-snapshot
Terretonin, ophiobolin, and drimaneterpenes with absolute configurations from an algicolous Aspergillus ustus
inferredcites →https://doi.org/10.1073/pnas.84.10.3081openalex-snapshot
Phytotoxins from the pathogenic fungi Drechslera maydis and Drechslera sorghicola
inferredcites →https://doi.org/10.1111/j.1745-4565.1988.tb00511.xopenalex-snapshot
SPICES AND HERBS: THEIR ANTIMICROBIAL ACTIVITY AND ITS DETERMINATION1
inferredcites →https://doi.org/10.1177/1934578x1200701102openalex-snapshot
Ophiobolin O and 6-Epi - Ophiobolin O, Two New Cytotoxic Sesterterpenes from the Marine Derived Fungus Aspergillus Sp
inferredcites →https://doi.org/10.1271/bbb1961.48.803openalex-snapshot
Isolation of ophiobolin A and its analogs as inhibitors to photosynthesis.
inferredcites →https://doi.org/10.1271/nogeikagaku1924.32.10_739openalex-snapshot
On the New Antibiotics “Ophiobolin”, produced by Ophiobolus Mi0yabeanus
inferredcites →https://doi.org/10.3390/molecules181214629openalex-snapshot
Bio-Activity and Dereplication-Based Discovery of Ophiobolins and Other Fungal Secondary Metabolites Targeting Leukemia Cells
inferredcites →https://doi.org/10.6023/cjoc201304039openalex-snapshot
New Marine Natural Products of Microbial Origin from 2010 to 2013
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4086887openalex-extracted
Cytotoxic Terpenoids from a Soil-Derived Fungus Aspergillus Calidoustus
inferred← citeshttps://doi.org/10.2139/ssrn.4818930openalex-extracted
Uplc-Q-Tof-Ms/Ms Analysis of Ophiobolins Sesterterpenoids to Mine New and Bioactive Analogues from Bipolaris Eleusines
inferred← citeshttps://doi.org/10.1002/cbdv.202100976openalex-snapshot
Exploration of Potent Cytotoxic Molecules from Fungi in Recent Past to Discover Plausible Anticancer Scaffolds
inferred← citeshttps://doi.org/10.1002/ejoc.202401020openalex-snapshot
Assembly of Thiazino[3,4‐ a ]Isoquinoline and Thiazepino[5,4‐ a ]Isoquinoline Frameworks from Isoquinolinium 1,4‐Zwitterionic Thiolates Through [5+1] and [5+2] Cycloaddition Reactions
inferred← citeshttps://doi.org/10.1002/slct.202507511openalex-snapshot
Synthesis of Functionalized 3,4‐Dihydro‐2 H ‐1,4‐Thiazines Through (3 + 3) Cyclization of Pyridinium 1,4‐Zwitterionic Thiolates With 2‐Bromoacetoanilides
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/10.1007/978-981-99-5696-8_5openalex-snapshot
Endolichenic Fungi, an Emerging Source of Bioactive Compounds: A Pharmaceutical Perspective
inferred← citeshttps://doi.org/10.1007/s00203-026-04752-6openalex-snapshot
Fungi as a source of anticancer agents: metabolic products and their functional implications
inferred← citeshttps://doi.org/10.1007/s00253-019-10103-xopenalex-snapshot
Production of sesterterpene ophiobolin by a bifunctional terpene synthase in Escherichia coli
inferred← citeshttps://doi.org/10.1007/s10600-026-05070-5openalex-snapshot
Secondary Metabolites from the Grape Endophytic Aspergillus pseudodeflectus
inferred← citeshttps://doi.org/10.1007/s11101-019-09624-0openalex-snapshot
Phytotoxins produced by pathogenic fungi of agrarian plants
inferred← citeshttps://doi.org/10.1016/j.bioorg.2022.105988openalex-snapshot
Structurally diverse metabolites from a soil-derived fungus Aspergillus calidoustus
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107772openalex-snapshot
Development of natural product-based targeted protein degraders as anticancer agents
inferred← citeshttps://doi.org/10.1016/j.bmcl.2019.02.007openalex-snapshot
Chemistry and biology of ophiobolin A and its congeners
inferred← citeshttps://doi.org/10.1016/j.cclet.2019.01.034openalex-snapshot
Pafuranones A and B, two dimeric polyketides from a rare marine algae-derived fungus Paraconiothyrium sp.
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.114081openalex-snapshot
Design and synthesis of marine sesterterpene analogues as novel estrogen receptor α degraders for breast cancer treatment
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.2022.114313openalex-snapshot
Synthesis and structure-activity relationship study of a potent MHO7 analogue as potential anti-triple negative breast cancer agent
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146291openalex-snapshot
Ustusteroids A−L: immunosuppressive and anti-inflammatory steroids from Aspergillus ustus 3.3904 guided by an OSMAC-based strategy
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.113011openalex-snapshot
Recent studies on terpenoids in Aspergillus fungi: Chemical diversity, biosynthesis, and bioactivity
inferred← citeshttps://doi.org/10.1016/j.phytochem.2022.113352openalex-snapshot
Cyophiobiolins A-D, ophiobolin sestertepenoids from Cytospora rhizophorae
inferred← citeshttps://doi.org/10.1016/j.phytochem.2024.114267openalex-snapshot
UPLC-Q-TOF-MS/MS analysis of ophiobolins sesterterpenoids and bioactive analogs from Bipolaris eleusines
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114802openalex-snapshot
1H NMR-guided isolation of ophiobolins from Bipolaris maydis and their bioactivities
inferred← citeshttps://doi.org/10.1016/j.phytochem.2026.114820openalex-snapshot
Soil-associated microorganisms: A natural source of biologically active compounds
inferred← citeshttps://doi.org/10.1016/j.prenap.2025.100334openalex-snapshot
A glance on the anticancer activities of natural products from marine derived fungi, Aspergillus sp.
inferred← citeshttps://doi.org/10.1016/s1875-5364(19)30116-5openalex-snapshot
Bipolarins A–H, eight new ophiobolin-type sesterterpenes with antimicrobial activity from fungus Bipolaris sp. TJ403-B1
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c03352openalex-snapshot
LC–MS/MS-Guided Molecular Networking for Targeted Discovery of Undescribed and Bioactive Ophiobolins from Bipolaris eleusines
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c08134openalex-snapshot
Bipoladien A, a Sesterterpenoid Containing an Undescribed 5/8/5/7 Carbon Skeleton from Bipolaris maydis
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c09030openalex-snapshot
Metabolites, Biotransformation, and Plant-Growth Dual Regulatory Activity from Aspergillus nishimurae Uncovered by the Fermentation Interaction with a Host
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00836openalex-snapshot
Drophiobiolins A and B, Bioactive Ophiobolan Sestertepenoids Produced byDreschslera gigantea
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00910openalex-snapshot
Antibacterial Drimane Sesquiterpenes from Aspergillus ustus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.3c01243openalex-snapshot
Asperustins A–J: Austocystins with Immunosuppressive and Cytotoxic Activities from Aspergillus ustus NRRL 5856
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.4c00385openalex-snapshot
Undobolins A–L, Ophiobolin-Type Sesterterpenoids from Aspergillus undulatus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.5c01414openalex-snapshot
Gigobolins A–C, New Ophiobolins with Anticancer Activity from the Phytopathogenic Fungus Drechslera gigantea
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00462openalex-snapshot
Ophiobolin-Type Sesterterpenoids from the Mangrove Endophytic Fungus Aspergillus sp. ZJ-68
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c03770openalex-snapshot
Direct Reaction of Nitroarenes and Thiols via Photodriven Oxygen Atom Transfer for Access to Sulfonamides
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00849openalex-snapshot
Metal-Free Photoredox Catalyzed Sulfonylation of Phenylhydrazines with Thiols
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b01567openalex-snapshot
Multicomponent Domino Synthesis of Cyclopenta[b]furan-2-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00581openalex-snapshot
Niduterpenoids A and B: Two Sesterterpenoids with a Highly Congested Hexacyclic 5/5/5/5/3/5 Ring System from the Fungus Aspergillus nidulans
inferred← citeshttps://doi.org/10.1038/s41429-020-00372-4openalex-snapshot
New naphthyl derivatives from Aspergillus californicus
inferred← citeshttps://doi.org/10.1039/c8qo00756jopenalex-snapshot
Secopaxilline A, an indole-diterpenoid derivative from an aciduric Penicillium fungus, its identification and semisynthesis
inferred← citeshttps://doi.org/10.1039/d0np00070aopenalex-snapshot
Sesterterpenoids: chemistry, biology, and biosynthesis
inferred← citeshttps://doi.org/10.1039/d1np00041aopenalex-snapshot
Secondary metabolites from mangrove-associated fungi: source, chemistry and bioactivities
inferred← citeshttps://doi.org/10.1039/d1ob02006dopenalex-snapshot
(±)-Usphenethylones A–C, three pairs of heterodimeric polyketide enantiomers from Aspergillus ustus 3.3904
inferred← citeshttps://doi.org/10.1039/d1ra01359aopenalex-snapshot
Recent updates on the bioactive compounds of the marine-derived genus Aspergillus
inferred← citeshttps://doi.org/10.1039/d3np00035dopenalex-snapshot
The incredible story of ophiobolin A and sphaeropsidin A: two fungal terpenes from wilt-inducing phytotoxins to promising anticancer compounds
inferred← citeshttps://doi.org/10.1039/d3ob00005bopenalex-snapshot
20- nor -Isopimarane and isopimarane diterpenoids produced by Aspergillus sp. WT03
inferred← citeshttps://doi.org/10.1039/d4np00041bopenalex-snapshot
Sesterterpenoids: sources, structural diversity, biological activity, and data management
inferred← citeshttps://doi.org/10.1080/10286020.2024.2428228openalex-snapshot
Talarindigotin A: a cytotoxic indigotin derivative, from the mangrove endophytic fungus Talaromyces amestolkiae SCNU-F0041
inferred← citeshttps://doi.org/10.1080/14786419.2019.1689496openalex-snapshot
New dihydrobenzofuranoid from the marine-derived fungus Aspergillus ustus KMM 4664
inferred← citeshttps://doi.org/10.1080/14786419.2021.1892673openalex-snapshot
Two new pyrone derivatives from the mangrove-derived endophytic fungus Aspergillus sydowii #2B
inferred← citeshttps://doi.org/10.1080/21501203.2024.2402309openalex-snapshot
Marine-derived fungi from the genus Aspergillus (Ascomycota) and their anticancer properties
inferred← citeshttps://doi.org/10.18926/55980openalex-snapshot
Unique antimicrobial activity of bioactive compound produced by Aspergillus ustus
inferred← citeshttps://doi.org/10.3389/fchem.2018.00344openalex-snapshot
Polyketides From the Endophytic Fungus Cladosporium sp. Isolated From the Mangrove Plant Excoecaria agallocha
inferred← citeshttps://doi.org/10.3389/fmicb.2018.02072openalex-snapshot
Molecular Networking-Based Metabolome and Bioactivity Analyses of Marine-Adapted Fungi Co-cultivated With Phytopathogens
inferred← citeshttps://doi.org/10.3389/fmicb.2020.00856openalex-snapshot
Novel Antimicrobial Compounds as Ophiobolin-Type Sesterterpenes and Pimarane-Type Diterpene From Bipolaris Species TJ403-B1
inferred← citeshttps://doi.org/10.3390/ijms23031903openalex-snapshot
The Biosynthesis and Transport of Ophiobolins in Aspergillus ustus 094102
inferred← citeshttps://doi.org/10.3390/md16050150openalex-snapshot
Two New Terpenoids from Talaromyces purpurogenus
inferred← citeshttps://doi.org/10.3390/md16090319openalex-snapshot
Lead Compounds from Mangrove-Associated Microorganisms
inferred← citeshttps://doi.org/10.3390/md17120667openalex-snapshot
Toxicity, Pharmacokinetics, and Gut Microbiome of Oral Administration of Sesterterpene MHO7 Derived from a Marine Fungus
inferred← citeshttps://doi.org/10.3390/md18060321openalex-snapshot
A Review of Terpenes from Marine-Derived Fungi: 2015–2019
inferred← citeshttps://doi.org/10.3390/md18110575openalex-snapshot
New Ophiobolins from the Deep-Sea Derived Fungus Aspergillus sp. WHU0154 and Their Anti-Inflammatory Effects
inferred← citeshttps://doi.org/10.3390/md20070408openalex-snapshot
Sesquiterpenoids from the Mangrove-Derived Aspergillus ustus 094102
inferred← citeshttps://doi.org/10.3390/md23080296openalex-snapshot
Salt-Adapted Microorganisms: A Promising Resource for Novel Anti-Cancer Drug Discovery
inferred← citeshttps://doi.org/10.3390/molecules28114381openalex-snapshot
Natural Bacterial and Fungal Peptides as a Promising Treatment to Defeat Lung Cancer Cells
inferred← citeshttps://doi.org/10.3390/molecules31020261openalex-snapshot
Advances in Natural Products from Mangrove-Associated Fungi Along the Indian Ocean Coast
inferred← citeshttps://doi.org/10.4018/979-8-3693-6972-2.ch014openalex-snapshot
Marine World of Terpenes Targeting Specific Cancers
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