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Microbial Transformations of Aryltetralone and Aryltetralin Lignans by Cunninghamella echinulata and Beauveria bassiana

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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/biof.5520190105openalex-snapshot

Hepatoprotective action of schisandrin B against carbon tetrachloride toxicity was mediated by both enhancement of mitochondrial glutathione status and induction of heat shock proteins in mice

inferredcites →https://doi.org/10.1016/0031-9422(91)84199-3openalex-snapshot

Biotransformation of Podophyllum lignans in cell suspension cultures of Forsythia intermedia

inferredcites →https://doi.org/10.1016/j.bmc.2008.03.030openalex-snapshot

Microbial metabolism of 1-aminoanthracene by Beauveria bassiana

inferredcites →https://doi.org/10.1016/j.phytochem.2006.02.007openalex-snapshot

Aryltetralol and aryltetralone lignans from Holostylis reniformis

inferredcites →https://doi.org/10.1016/s0031-9422(00)90836-7openalex-snapshot

Biotransformation of lignans: a specific microbial oxidation of (+)-eudesmin and (+)-magnolin by Aspergillus niger

inferredcites →https://doi.org/10.1016/s0141-0229(03)00207-2openalex-snapshot

The synthesis of buprenorphine intermediates by regioselective microbial N- and O-demethylation reactions using Cunninghamella echinulata NRRL 1384

inferredcites →https://doi.org/10.1021/np0302697openalex-snapshot

Tetrahydrofuran Lignans from Nectandra m egapotamica with Trypanocidal Activity

inferredcites →https://doi.org/10.1021/np050283eopenalex-snapshot

Bioactive Tetrahydrofuran Lignans from Peperomia dindygulensis

inferredcites →https://doi.org/10.1021/np050457sopenalex-snapshot

Bioactive Compounds from Peperomia pellucida

inferredcites →https://doi.org/10.1021/np0580309openalex-snapshot

Microbial Transformation of Curvularin

inferredcites →https://doi.org/10.1021/np060339kopenalex-snapshot

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

inferredcites →https://doi.org/10.1021/np50006a010openalex-snapshot

Microbial Transformations of Natural Antitumor Agents. 9. O-Demethylation of 9-Methoxyellipticine

inferredcites →https://doi.org/10.1021/np9003678openalex-snapshot

Oxygenated Lignans from the Fruits of Schisandra arisanensis

inferredcites →https://doi.org/10.1021/np9601667openalex-snapshot

Two New Lignans, Interiotherins A and B, as Anti-HIV Principles from Kadsura interior

inferredcites →https://doi.org/10.1021/np980136zopenalex-snapshot

Antiviral Activity of Lignans

inferredcites →https://doi.org/10.1039/b514045popenalex-snapshot

An update on bioactive plant lignans

inferredcites →https://doi.org/10.1055/s-2006-961473openalex-snapshot

Anti-Oxidant Activity of Dibenzocyclooctene Lignans Isolated from Schisandraceae

inferredcites →https://doi.org/10.1055/s-2007-969461openalex-snapshot

Schisandrone, a New 4-Aryltetralone Lignan fromSchisandra sphenanthera

inferredcites →https://doi.org/10.1080/10242420600792169openalex-snapshot

Selective 4′-O-methylglycosylation of the pentahydroxy-flavonoid quercetin byBeauveria bassianaATCC 7159

inferredcites →https://doi.org/10.1128/aac.01344-06openalex-snapshot

Antiplasmodial Activity of Aryltetralone Lignans from Holostylis reniformis

inferredcites →https://doi.org/10.1139/v87-087openalex-snapshot

Side chain hydroxylation of aromatic compounds by fungi.: 1. Products and stereochemistry

inferredcites →https://doi.org/10.1271/bbb.60429openalex-snapshot

Antibacterial Activity of a Virgatusin-Related Compound

inferredcites →https://doi.org/10.1271/bbb.60696openalex-snapshot

Antifungal Activity of Tetra-Substituted Tetrahydrofuran Lignan, (−)-Virgatusin, and Its Structure-Activity Relationship

inferredcites →https://doi.org/10.1351/pac200072081493openalex-snapshot

Nomenclature of Lignans and Neolignans (IUPAC Recommendations 2000)

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.4592227openalex-extracted

Phenylpropanoids from the Leaves of Styrax Japonicus and Theiranti-Inflammatory Activity

inferred← citeshttps://doi.org/10.1016/j.fitote.2023.105774openalex-snapshot

Lignans from the leaves of Styrax japonicus and their anti-inflammatory activity

inferred← citeshttps://doi.org/10.1016/j.phytol.2015.06.001openalex-snapshot

Aryltetralols from Holostylis reniformis and syntheses of lignan analogous

inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.06.015openalex-snapshot

Synthesis of various lignans via the rearrangements of 1,4-diarylbutane-1,4-diols

inferred← citeshttps://doi.org/10.1021/acs.orglett.5b03696openalex-snapshot

Synthesis of Substituted Tetralins and Benzosuberans via BF3·OEt2-Mediated Formal (4 + 2) and (5 + 2) Stereocontrolled Cycloaddition of 4-Alkenols with Veratrol

inferred← citeshttps://doi.org/10.1021/acs.orglett.6b00603openalex-snapshot

Synthesis of 1-Aryltetralins and 1-Arylnaphthalenes via (4 + 2) Annulation of β-Ketosulfones with Styryl Bromides

inferred← citeshttps://doi.org/10.1021/np4010536openalex-snapshot

Lignans from the Fruit of Schisandra glaucescens with Antioxidant and Neuroprotective Properties

inferred← citeshttps://doi.org/10.1039/c4np00054dopenalex-snapshot

Discovering the secondary metabolite potential encoded within entomopathogenic fungi

inferred← citeshttps://doi.org/10.1039/c6np00021eopenalex-snapshot

Recent advances in research on lignans and neolignans

inferred← citeshttps://doi.org/10.1039/c6sc04762aopenalex-snapshot

Triflimide-catalyzed allylsilane annulations of benzylic alcohols for the divergent synthesis of indanes and tetralins

inferred← citeshttps://doi.org/10.1039/c7ob00749copenalex-snapshot

Asymmetric synthesis of ent-fragransin C 1

inferred← citeshttps://doi.org/10.1055/s-0036-1588788openalex-snapshot

Efficient Total Synthesis of (±)-Isoguaiacin and (±)-Isogalbulin

inferred← citeshttps://doi.org/10.1177/1934578x1300800802openalex-snapshot

Microbial Biotransformation of 16α,17-Epoxy- Ent -kaurane-19-oic acid by Beauveria Sulfurescens ATCC 7159-F

inferred← citeshttps://doi.org/10.1177/1934578x1400900607openalex-snapshot

Stereo and Regioselective Microbial Reduction of the Clerodane Diterpene 3,12-Dioxo-15,16-epoxy-4-hydroxycleroda-13(16),14-diene

inferred← citeshttps://doi.org/10.3390/molecules171214046openalex-snapshot

4,5-Seco-Guaiane and a Nine-Membered Sesquiterpene Lactone from Holostylis reniformis

inferred← citeshttps://doi.org/10.3390/molecules28010302openalex-snapshot

Chemistry and Biological Activities of Naturally Occurring and Structurally Modified Podophyllotoxins

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