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Microbial Transformation of Amino- and Hydroxyanthraquinones by Beauveria bassiana ATCC 7159

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cber.19761090632openalex-snapshot
Mikrobiologische Umwandlungen nichtsteroider Strukturen, VII. Mikrobielle Glucosidierung einer phenolischen Hydroxylgruppe
inferredcites →https://doi.org/10.1016/0166-3542(92)90091-iopenalex-snapshot
Evaluation of the antiviral activity of anthraquinones, anthrones and anthraquinone derivatives against human cytomegalovirus
inferredcites →https://doi.org/10.1016/s0378-8741(00)00195-1openalex-snapshot
Antifungal activity of anthraquinone derivatives from Rheum emodi
inferredcites →https://doi.org/10.1016/s0968-0896(97)00094-1openalex-snapshot
Microbial biotransformations of a synthetic immunomodulating agent, HR325
inferredcites →https://doi.org/10.1016/s1381-1177(02)00081-4openalex-snapshot
Microbial C-hydroxylation and β-4-O-methylglucosidation of methyl-benzamide 7-azanorbornane ethers with Beauveria bassiana
inferredcites →https://doi.org/10.1021/jm990084qopenalex-snapshot
2,7-Disubstituted Amidofluorenone Derivatives as Inhibitors of Human Telomerase
inferredcites →https://doi.org/10.1021/np0580309openalex-snapshot
Microbial Transformation of Curvularin
inferredcites →https://doi.org/10.1038/sj.bjp.0703427openalex-snapshot
Effect of cytochrome P‐450 inhibitors econazole, bifonazole and clotrimazole on prostanoid formation
inferredcites →https://doi.org/10.1081/ncn-100107200openalex-snapshot
SYNTHESIS AND ANTIVIRAL EVALUATION OF N-GLYCOSIDES DERIVED FROM 6-AMINO-3-ARYL-2-METHYL-4-(3H)-QUINAZOLINONES
inferredcites →https://doi.org/10.1135/cccc19821807openalex-snapshot
Gas chromatographic analysis of metabolites of trees damaged by exhalations
inferredcites →https://doi.org/10.7164/antibiotics.50.18openalex-snapshot
Brasiliquinones A, B and C, New Benz(a)anthraquinone Antibiotics from Nocardia brasiliensis. I. Producing Strain, Isolation and Biological Activities of the Antibiotics.

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.4121265openalex-extracted
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Highly Efficient and Regio‐selective Glucosylation of 25(S) Ruscogenin by Gliocladium deliquescens NRRL1086
inferred← citeshttps://doi.org/10.1007/978-3-642-11458-8_14openalex-snapshot
Fungal Biotransformations in Pharmaceutical Sciences
inferred← citeshttps://doi.org/10.1007/978-3-7091-0140-7_3openalex-snapshot
Combinatorial and Synthetic Biosynthesis in Actinomycetes
inferred← citeshttps://doi.org/10.1007/s00253-021-11716-xopenalex-snapshot
A highly versatile fungal glucosyltransferase for specific production of quercetin-7-O-β-d-glucoside and quercetin-3-O-β-d-glucoside in different hosts
inferred← citeshttps://doi.org/10.1007/s13205-025-04456-6openalex-snapshot
Beauveria bassiana as a versatile biocatalyst: advances in regioselective hydroxylation and applications in biological control
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104300openalex-snapshot
Metabolites with phytopathogenic fungi inhibitory activities from the mangrove endophytic fungus Botryosphaeria ramose
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.03.030openalex-snapshot
Microbial metabolism of 1-aminoanthracene by Beauveria bassiana
inferred← citeshttps://doi.org/10.1016/j.fitote.2022.105247openalex-snapshot
Creating Diverse Glycosides of 2'-Hydroxyflavone Through Microbial Glycosylation
inferred← citeshttps://doi.org/10.1016/j.jbiosc.2024.05.009openalex-snapshot
Enhancing the physicochemical properties and bioactivities of 2′-hydroxyflavanone through fungal biotransformation
inferred← citeshttps://doi.org/10.1016/j.molcatb.2013.10.008openalex-snapshot
Exploring the glycosylation capabilities of Gliocladium deliquescens NRRL 1086 on hydroxyl benzophenones
inferred← citeshttps://doi.org/10.1016/j.phytol.2020.04.011openalex-snapshot
Isolation and selective glycosylation of antisalmonellal anthraquinones from the stem bark of Morinda lucida Benth. (Rubiaceae)
inferred← citeshttps://doi.org/10.1016/s0076-6879(09)04812-5openalex-snapshot
Chapter 12 The Power of Glycosyltransferases to Generate Bioactive Natural Compounds
inferred← citeshttps://doi.org/10.1021/mp7001544openalex-snapshot
In Vivo and In Vitro Production Options for Fungal Secondary Metabolites
inferred← citeshttps://doi.org/10.1021/np070262fopenalex-snapshot
Cytotoxic and Antihaptotactic Beauvericin Analogues from Precursor-Directed Biosynthesis with the Insect Pathogen Beauveria bassiana ATCC 7159
inferred← citeshttps://doi.org/10.1021/np100607sopenalex-snapshot
Microbial Transformations of Aryltetralone and Aryltetralin Lignans by Cunninghamella echinulata and Beauveria bassiana
inferred← citeshttps://doi.org/10.1039/c4np00054dopenalex-snapshot
Discovering the secondary metabolite potential encoded within entomopathogenic fungi
inferred← citeshttps://doi.org/10.1073/pnas.1716046115openalex-snapshot
Methylglucosylation of aromatic amino and phenolic moieties of drug-like biosynthons by combinatorial biosynthesis
inferred← citeshttps://doi.org/10.1128/aem.01652-13openalex-snapshot
Tracking Down Biotransformation to the Genetic Level: Identification of a Highly Flexible Glycosyltransferase from Saccharothrix espanaensis
inferred← citeshttps://doi.org/10.1177/1934578x1000500119openalex-snapshot
4′-O-Methylglycosylation of Curcumin by Beauveria bassiana
inferred← citeshttps://doi.org/10.1177/1934578x1000500524openalex-snapshot
Structure Determination of Two New Monocillin I Derivatives
inferred← citeshttps://doi.org/10.1177/1934578x1100600216openalex-snapshot
Generation of two New Macrolactones through Sequential Biotransformation of Dihydroresorcylide
inferred← citeshttps://doi.org/10.1248/cpb.56.1253openalex-snapshot
Microbial Metabolism of Biologically Active Secondary Metabolites from Nerium oleander L.
inferred← citeshttps://doi.org/10.1271/bbb.120223openalex-snapshot
Specific 5-Hydroxylation of Piperlongumine byBeauveria bassianaATCC 7159
inferred← citeshttps://doi.org/10.13005/bbra/1167openalex-snapshot
Microbial Transformation of Bioactive Anthraquinones ? A Review
inferred← citeshttps://doi.org/10.3109/10242420903497354openalex-snapshot
Glycosylation of (–)-maackiain byBeauveria bassianaandCunninghamella echinulatavar.elegans
inferred← citeshttps://doi.org/10.3390/md9050832openalex-snapshot
Three Bianthraquinone Derivatives from the Mangrove Endophytic Fungus Alternaria sp. ZJ9-6B from the South China Sea
inferred← citeshttps://doi.org/10.3390/molecules22071230openalex-snapshot
The Influence of Glycosylation of Natural and Synthetic Prenylated Flavonoids on Binding to Human Serum Albumin and Inhibition of Cyclooxygenases COX-1 and COX-2
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