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Balticolid: A New 12-Membered Macrolide with Antiviral Activity from an Ascomycetous Fungus of Marine Origin
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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/cbdv.200800150openalex-snapshot
Balticols A–F, New Naphthalenone Derivatives with Antiviral Activity, from an Ascomycetous Fungus
inferredcites →https://doi.org/10.1016/0031-9422(95)00414-3openalex-snapshot
Twelve-membered lactones produced by cladosporium tenuissimum and the plant growth retardant activity of cladospolide B
inferredcites →https://doi.org/10.1016/s0040-4039(00)95093-7openalex-snapshot
Structure of patulolide a, a new macrolide from mutants
inferredcites →https://doi.org/10.1021/ja00011a006openalex-snapshot
High-field FT NMR application of Mosher's method. The absolute configurations of marine terpenoids
inferredcites →https://doi.org/10.1021/ja00783a034openalex-snapshot
Nuclear magnetic resonance enantiomer regents. Configurational correlations via nuclear magnetic resonance chemical shifts of diastereomeric mandelate, O-methylmandelate, and .alpha.-methoxy-.alpha.-trifluoromethylphenylacetate (MTPA) esters
inferredcites →https://doi.org/10.1021/np000401sopenalex-snapshot
New Macrolides and Furan Carboxylic Acid Derivative from the Sponge-Derived Fungus Cladosporium herbarum
inferredcites →https://doi.org/10.1021/np0504964openalex-snapshot
Chloriolide, a 12-Membered Macrolide from Chloridium virescens var. chlamydosporum (NRRL 37636)
inferredcites →https://doi.org/10.1038/nprot.2007.354openalex-snapshot
Mosher ester analysis for the determination of absolute configuration of stereogenic (chiral) carbinol carbons
inferredcites →https://doi.org/10.1139/v71-330openalex-snapshot
11-Hydroxy-trans-8-dodecenoic Acid Lactone, a 12-Membered-Ring Compound from a Fungus
inferredcites →https://doi.org/10.1271/bbb1961.49.731openalex-snapshot
New plant growth regulators, cladospolide A and B, macrolides produced by Cladosporium cladosporioides.
inferredcites →https://doi.org/10.7164/antibiotics.39.629openalex-snapshot
New macrolides from Penicillium urticae mutant S11R59.
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.2020.112462zenodo-depositor-declared
Thiocladospolides F-J, antibacterial sulfur containing 12-membered macrolides from the mangrove endophytic fungus Cladosporium oxysporum HDN13-314
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Harnessing the Chemical and Genetic Diversities of Marine Microorganisms for Medical Applications
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Mangrove Microbiome as a Source of Antiviral Drugs
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inferred← citeshttps://doi.org/10.1007/s00606-016-1350-2openalex-snapshot
Biatriospora (Ascomycota: Pleosporales) is an ecologically diverse genus including facultative marine fungi and endophytes with biotechnological potential
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inferred← citeshttps://doi.org/10.1016/b978-0-12-821006-2.00012-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-444-63359-0.00003-3openalex-snapshot
Classical Methodologies for Preparation of Extracts and Fractions
inferred← citeshttps://doi.org/10.1016/b978-0-444-63460-3.00007-9openalex-snapshot
The Chemistry and Bioactivity of Macrolides from Marine Microorganisms
inferred← citeshttps://doi.org/10.1016/j.cbi.2022.110072openalex-snapshot
Therapeutic potential of marine macrolides: An overview from 1990 to 2022
inferred← citeshttps://doi.org/10.1016/j.cdc.2023.101000openalex-snapshot
Total synthesis of the proposed structure of Pandangolide 1
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.112790openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fitote.2019.104246openalex-snapshot
Thiocladospolide E and cladospamide A, novel 12-membered macrolide and macrolide lactam from mangrove endophytic fungus Cladosporium sp. SCNU-F0001
inferred← citeshttps://doi.org/10.1016/j.mencom.2018.09.017openalex-snapshot
Original catalytic synthesis of macrodiolides containing a 1Z,5Z-diene moiety
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136723openalex-snapshot
Asepterpenedol A, a novel indole sesquiterpene with a rare 7/6/5/5/6/6-hexacyclic scaffold from a marine-derived fungus Chloridium sp. NBU3282
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.tet.2018.07.031openalex-snapshot
Targeted synthesis of macrodiolides containing bis-methylene-separated Z-double bonds and their antitumor activity in vitro
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.10.027openalex-snapshot
The first total synthesis of a 12-membered macrolide balticolid
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.09.126openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151027openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.trac.2011.10.014openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cb500284topenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo400861jopenalex-snapshot
Structure, Absolute Configuration, and Conformational Study of 12-Membered Macrolides from the Fungus Dendrodochium sp. Associated with the Sea Cucumber Holothuria nobilis Selenka
inferred← citeshttps://doi.org/10.1038/s41467-024-49587-1openalex-snapshot
Discovering type I cis-AT polyketides through computational mass spectrometry and genome mining with Seq2PKS
inferred← citeshttps://doi.org/10.1039/d1ra04576hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1080/00397911.2023.2220443openalex-snapshot
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inferred← citeshttps://doi.org/10.1177/2040206617705500openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s13071-024-06157-0openalex-snapshot
Anti-Toxoplasma gondii effect of tylosin in vitro and in vivo
inferred← citeshttps://doi.org/10.20944/preprints201805.0214.v1openalex-snapshot
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Bioactive compounds from fungi with antiviral activities: Mechanism of action and biosynthetic pathways
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inferred← citeshttps://doi.org/10.3390/biom10071007openalex-snapshot
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Early Intervention in Herpes Simplex Virus-1 Replication in Vitro with Allenic Macrolide Archangiumide
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Additional file 1 of Anti-Toxoplasma gondii effect of tylosin in vitro and in vivo
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