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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
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/bcmd.1997.0155openalex-snapshot
Inhibition of the ABL Kinase Activity Blocks the Proliferation of BCR/ABL+Leukemic Cells and Induces Apoptosis
inferredcites →https://doi.org/10.1016/0031-9422(88)80421-7openalex-snapshot
6-Epiophiobolin A and 3-anhydro-6-epiophiobolin A—host specific phytotoxins of Drechslera maydis (race T)
inferredcites →https://doi.org/10.1016/j.bmcl.2011.10.079openalex-snapshot
The novel agent ophiobolin O induces apoptosis and cell cycle arrest of MCF-7 cells through activation of MAPK signaling pathways
inferredcites →https://doi.org/10.1016/j.fitote.2011.10.013openalex-snapshot
Polyketides with antimicrobial activity from the solid culture of an endolichenic fungus Ulocladium sp.
inferredcites →https://doi.org/10.1016/j.semcancer.2006.07.015openalex-snapshot
The Myc oncoprotein as a therapeutic target for human cancer
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/j.tetlet.2007.05.151openalex-snapshot
Anhydrocochlioquinone A, a new antitumor compound from Bipolaris oryzae
inferredcites →https://doi.org/10.1016/s0024-3205(00)00668-8openalex-snapshot
The biology of ophiobolins
inferredcites →https://doi.org/10.1021/jf052843lopenalex-snapshot
Herbicidal Potential of Ophiobolins Produced by Drechslera gigantea
inferredcites →https://doi.org/10.1021/np200906sopenalex-snapshot
Natural Products As Sources of New Drugs over the 30 Years from 1981 to 2010
inferredcites →https://doi.org/10.1021/np50115a009openalex-snapshot
Microbial Metabolites of Ophiobolin A and Antimicrobial Evaluation of Ophiobolins
inferredcites →https://doi.org/10.1038/nrc2126openalex-snapshot
Second generation inhibitors of BCR-ABL for the treatment of imatinib-resistant chronic myeloid leukaemia
inferredcites →https://doi.org/10.1038/nrmicro2319openalex-snapshot
Antibiotic resistance and its cost: is it possible to reverse resistance?
inferredcites →https://doi.org/10.1107/s0567740868004206openalex-snapshot
X-ray studies of C25 terpenoids. I. The crystal structure of ophiobolin methoxybromide
inferredcites →https://doi.org/10.1158/1541-7786.mcr-10-0356openalex-snapshot
MYC in Chronic Myeloid Leukemia: Induction of Aberrant DNA Synthesis and Association with Poor Response to Imatinib
inferredcites →https://doi.org/10.18388/abp.2005_3421openalex-snapshot
Strategies for overcoming ABC-transporters-mediated multidrug resistance (MDR) of tumor cells.
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.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/ange.201905966openalex-snapshot
Bipolarolides A–G: Ophiobolin‐Derived Sesterterpenes with Three New Carbon Skeletons from Bipolaris sp. TJ403‐B1
inferred← citeshttps://doi.org/10.1002/anie.201905966openalex-snapshot
Bipolarolides A–G: Ophiobolin‐Derived Sesterterpenes with Three New Carbon Skeletons from Bipolaris sp. TJ403‐B1
inferred← citeshttps://doi.org/10.1002/chin.201340201openalex-snapshot
ChemInform Abstract: 3‐Anhydro‐6‐hydroxy‐ophiobolin A (I), a New Sesterterpene Inhibiting the Growth of Methicillin‐Resistant Staphylococcus aureus and Inducing the Cell Death by Apoptopsis on K562, from the Phytopathogenic Fungus Bipolaris oryzae.
inferred← citeshttps://doi.org/10.1002/slct.202002385openalex-snapshot
Bioreduction of Gold Ions from Anisotropic to Isotropic Nanostructures by NADPH‐Dependent Reductase from Bipolaris oryzae
inferred← citeshttps://doi.org/10.1007/s00253-021-11226-wopenalex-snapshot
Antibacterial polyene-polyol macrolides and cyclic peptides from the marine-derived Streptomyces sp. MS110128
inferred← citeshttps://doi.org/10.1007/s13225-017-0386-0openalex-snapshot
Notes for genera: Ascomycota
inferred← citeshttps://doi.org/10.1007/s13238-016-0325-yopenalex-snapshot
3-Anhydro-6-hydroxy-ophiobolin A displays high in vitro and in vivo efficacy against influenza A virus infection
inferred← citeshttps://doi.org/10.1016/b978-0-444-63504-4.00018-9openalex-snapshot
Secondary Metabolites From Endophytic Fungi and Their Biological Activities
inferred← citeshttps://doi.org/10.1016/j.bmcl.2015.02.030openalex-snapshot
3-Anhydro-6-hydroxy-ophiobolin A, a fungal sesterterpene from Bipolaris oryzae induced autophagy and promoted the degradation of α-synuclein in PC12 cells
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.2025.110904openalex-snapshot
Ophiobolin-type sesterterpenoids with unprecedented chemical architectures from Bipolaris oryzae and their inflammatory activity
inferred← citeshttps://doi.org/10.1016/j.fbr.2018.09.002openalex-snapshot
Diversity of natural products of the genera Curvularia and Bipolaris
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/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.jnatprod.4c00658openalex-snapshot
Maydisens, Sesterterpenoids with Anti-MDR Activity from Bipolaris maydis
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.7b00335openalex-snapshot
Ophiobolins from the Mangrove Fungus Aspergillus ustus
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.9b00744openalex-snapshot
Bipolaricins A–I, Ophiobolin-Type Tetracyclic Sesterterpenes from a Phytopathogenic Bipolaris sp. Fungus
inferred← citeshttps://doi.org/10.1021/acs.joc.0c01127openalex-snapshot
Catalyst-free Tandem 1,3-Dipolar Cycloaddition/Aldol Condensation: Diastereoselective Construction of the Azatetraquinane Skeleton
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c02272openalex-snapshot
A Stereoselective Photoinduced Cycloisomerization Inspired by Ophiobolin A
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/10.1039/d0np00070aopenalex-snapshot
Sesterterpenoids: chemistry, biology, and biosynthesis
inferred← citeshttps://doi.org/10.1039/d4np00041bopenalex-snapshot
Sesterterpenoids: sources, structural diversity, biological activity, and data management
inferred← citeshttps://doi.org/10.1039/d4qo02057jopenalex-snapshot
Bipolarsterol A, a steroid with an unprecedented 6/5/6/5 carbon skeleton from the phytopathogenic fungus Bipolaris oryzae
inferred← citeshttps://doi.org/10.1055/a-0593-6030openalex-snapshot
Botryane Sesquiterpenoids, Cyclopentadepsipeptides, Xanthones, and Trichothecenes from Trichoderma oligosporum
inferred← citeshttps://doi.org/10.1111/tpj.13064openalex-snapshot
Arabidopsis thaliana isoprenyl diphosphate synthases produce the C25 intermediate geranylfarnesyl diphosphate
inferred← citeshttps://doi.org/10.14232/phd.3979openalex-snapshot
Fonalas gombák másodlagosmetabolit-termelésének tanulmányozása
inferred← citeshttps://doi.org/10.31296/cmr.8openalex-snapshot
A Brief Review on Structure-Bioactivity Relationship Study of Ophiobolins and Derivatives
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/jof8101080openalex-snapshot
Research Progress on Fungal Sesterterpenoids Biosynthesis
inferred← citeshttps://doi.org/10.3390/jof9020254openalex-snapshot
Diversity, Lifestyle, Genomics, and Their Functional Role of Cochliobolus, Bipolaris, and Curvularia Species in Environmental Remediation and Plant Growth Promotion under Biotic and Abiotic Stressors
inferred← citeshttps://doi.org/10.3390/md15070229openalex-snapshot
The Biological Activities of Sesterterpenoid-Type Ophiobolins
inferred← citeshttps://doi.org/10.3390/molecules180911338openalex-snapshot
Anticancer and Antifungal Compounds from Aspergillus, Penicillium and Other Filamentous Fungi
inferred← citeshttps://doi.org/10.3390/molecules181214629openalex-snapshot
Bio-Activity and Dereplication-Based Discovery of Ophiobolins and Other Fungal Secondary Metabolites Targeting Leukemia Cells
inferred← citeshttps://doi.org/10.3390/molecules26040810openalex-snapshot
Development and Effects of Influenza Antiviral Drugs
inferred← citeshttps://doi.org/10.3390/molecules31071206openalex-snapshot
From Phytotoxin to Cell-Death Probe: Ophiobolin A and Related Sesterterpenoids in Membrane Stress and Non-Apoptotic Cell Death
inferred← citeshttps://doi.org/10.3390/toxins11120683openalex-snapshot
Screening Mold Colonies by Using Two Toxicity Assays Revealed Indoor Strains of Aspergillus calidoustus Producing Ophiobolins G and K
inferred← citeshttps://doi.org/10.3390/toxins6092857openalex-snapshot
Ophiobolin A from Bipolaris oryzae Perturbs Motility and Membrane Integrities of Porcine Sperm and Induces Cell Death on Mammalian Somatic Cell Lines
inferred← citeshttps://doi.org/10.3390/v14112452openalex-snapshot
Antiviral Potential of Natural Resources against Influenza Virus Infections
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