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The enzyme‐oriented regulation of theaflavin‐3, 3 ′ ‐digallate synthesis and the accurate determination of its yield

https://doi.org/10.1111/ijfs.14429
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Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

2 of the 31 references listed on this page are in the Retraction Watch database as retracted (export 2026-11-11): 10.1016/j.febslet.2009.10.081 (notice 2024-12-13), 10.1016/j.lfs.2007.07.033 (notice 2022-08-05).

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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/jsfa.2740630409openalex-snapshot
The role of (−)‐epicatechin and polyphenol oxidase in the coupled oxidative breakdown of theaflavins
inferredcites →https://doi.org/10.1002/jsfa.7003openalex-snapshot
The fungal laccase‐catalyzed oxidation of EGCG and the characterization of its products
inferredcites →https://doi.org/10.1007/s00726-005-0298-2openalex-snapshot
When quinones meet amino acids: chemical, physical and biological consequences
inferredcites →https://doi.org/10.1016/j.bmc.2003.10.024openalex-snapshot
Enzymatic synthesis of tea theaflavin derivatives and their anti-inflammatory and cytotoxic activities
inferredcites →https://doi.org/10.1016/j.febslet.2009.10.081openalex-snapshot
RETRACTED: Theaflavins retard human breast cancer cell migration by inhibiting NF‐κB via p53‐ROS cross‐talk
inferredcites →https://doi.org/10.1016/j.foodchem.2010.03.027openalex-snapshot
Effective use of reducing agents and nanoparticle encapsulation in stabilizing catechins in alkaline solution
inferredcites →https://doi.org/10.1016/j.ijbiomac.2016.10.072openalex-snapshot
Effective synthesis of theaflavin-3,3′-digallate with epigallocatechin-3- O -gallate and epicatechin gallate as substrates by using immobilized pear polyphenol oxidase
inferredcites →https://doi.org/10.1016/j.jff.2014.09.003openalex-snapshot
Theaflavin-3, 3′-digallate, a black tea polyphenol, attenuates adipocyte-activated inflammatory response of macrophage associated with the switch of M1/M2-like phenotype
inferredcites →https://doi.org/10.1016/j.lfs.2007.07.033openalex-snapshot
RETRACTED: Theaflavins induce G2/M arrest by modulating expression of p21waf1/cip1, cdc25C and cyclin B in human prostate carcinoma PC-3 cells
inferredcites →https://doi.org/10.1016/j.molcatb.2017.03.009openalex-snapshot
Specificity of tyrosinase-catalyzed synthesis of theaflavins
inferredcites →https://doi.org/10.1016/j.nut.2010.01.019openalex-snapshot
Prevention of diet-induced obesity by dietary black tea polyphenols extract in vitro and in vivo
inferredcites →https://doi.org/10.1016/j.procbio.2017.02.002openalex-snapshot
Highly efficient synthesis of theaflavins by tyrosinase from mushroom and its application to theaflavin related compounds
inferredcites →https://doi.org/10.1016/j.tet.2003.08.025openalex-snapshot
Production of theasinensins A and D, epigallocatechin gallate dimers of black tea, by oxidation–reduction dismutation of dehydrotheasinensin A
inferredcites →https://doi.org/10.1016/j.tet.2006.03.021openalex-snapshot
A new mechanism for oxidation of epigallocatechin and production of benzotropolone pigments
inferredcites →https://doi.org/10.1016/j.tet.2015.03.016openalex-snapshot
Selective oxidation of pyrogallol-type catechins with unripe fruit homogenate of Citrus unshiu and structural revision of oolongtheanins
inferredcites →https://doi.org/10.1016/j.tetlet.2014.07.092openalex-snapshot
Synthesis of theaflavins with Camellia sinensis cell culture and inhibition of increase in blood sugar values in high-fat diet mice subjected to sucrose or glucose loading
inferredcites →https://doi.org/10.1016/j.tetlet.2015.07.037openalex-snapshot
Oxidation mechanism of black tea pigment theaflavin by peroxidase
inferredcites →https://doi.org/10.1016/s0304-4165(01)00230-6openalex-snapshot
Kinetic analysis and mechanistic aspects of autoxidation of catechins
inferredcites →https://doi.org/10.1021/jf011301aopenalex-snapshot
Synthesis of Theaflavin from Epicatechin and Epigallocatechin by Plant Homogenates and Role of Epicatechin Quinone in the Synthesis and Degradation of Theaflavin
inferredcites →https://doi.org/10.1021/jf0627672openalex-snapshot
α-Glucosidase Inhibitory Profile of Catechins and Theaflavins
inferredcites →https://doi.org/10.1021/jf970042fopenalex-snapshot
Oxidation of Chlorogenic Acid, Catechins, and 4-Methylcatechol in Model Solutions by Combinations of Pear (Pyrus communis Cv. Williams) Polyphenol Oxidase and Peroxidase: A Possible Involvement of Peroxidase in Enzymatic Browning
inferredcites →https://doi.org/10.1021/np020245kopenalex-snapshot
Accumulation of Epigallocatechin Quinone Dimers during Tea Fermentation and Formation of Theasinensins
inferredcites →https://doi.org/10.1080/00021369.1987.10868292openalex-snapshot
Effects of ( – )-Epicatechin on Oxidation of Theaflavins by Polyphenol Oxidase from Tea Leaves
inferredcites →https://doi.org/10.1080/16546628.2017.1400340openalex-snapshot
Pre-treated theaflavin-3,3′-digallate has a higher inhibitory effect on the HCT116 cell line
inferredcites →https://doi.org/10.1093/carcin/20.4.733openalex-snapshot
Suppression of extracellular signals and cell proliferation by the black tea polyphenol, theaflavin-3,3′-digallate
inferredcites →https://doi.org/10.1093/carcin/bgp240openalex-snapshot
Theaflavins target Fas/caspase-8 and Akt/pBad pathways to induce apoptosis in p53-mutated human breast cancer cells
inferredcites →https://doi.org/10.1111/ijfs.13849openalex-snapshot
In situ enzymatic synthesis and purification of theaflavin‐3,3′‐digallate monomer and incorporation into nanoliposome
inferredcites →https://doi.org/10.1248/cpb.55.1768openalex-snapshot
Structures of Epicatechin Gallate Trimer and Tetramer Produced by Enzymatic Oxidation
inferredcites →https://doi.org/10.1248/cpb.56.266openalex-snapshot
Polymer-Like Polyphenols of Black Tea and Their Lipase and Amylase Inhibitory Activities
inferredcites →https://doi.org/10.2174/09298673113209990158openalex-snapshot
Drug-Delivery Systems of Green Tea Catechins for Improved Stability and Bioavailability
inferredcites →https://doi.org/10.3390/ijms11010014openalex-snapshot
Chemistry of Secondary Polyphenols Produced during Processing of Tea and Selected Foods

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.4756343openalex-extracted
The Enzymatic Synthesis of Theaflavin-3-Gallate Oxidation Product and its Determination
inferred← citeshttps://doi.org/10.1002/ajoc.202300327openalex-snapshot
Effective Enzymatic Synthesis of Benzotropolone and Formation Mechanism of Its Bicyclo[3.2.1]octane‐type Intermediate
inferred← citeshttps://doi.org/10.1002/fsn3.70762openalex-snapshot
A Comprehensive Review of Theaflavins: Physiological Activities, Synthesis Techniques, and Future Challenges
inferred← citeshttps://doi.org/10.1007/s12257-021-0145-7openalex-snapshot
Production of Theasinensin A Using Laccase as Antioxidant and Antiaging Agent
inferred← citeshttps://doi.org/10.1016/j.bmcl.2025.130532openalex-snapshot
Synthesis of theaflavin-3′-gallate oxidation products and their impact on α-amylase activity
inferred← citeshttps://doi.org/10.1016/j.cofs.2026.101455openalex-snapshot
Advances in diversity and formation mechanisms of black tea polyphenols
inferred← citeshttps://doi.org/10.1016/j.foodchem.2026.149568openalex-snapshot
Theaflavins as characteristic polyphenols formed during black tea fermentation: Formation chemistry, functional properties, and future food applications
inferred← citeshttps://doi.org/10.1016/j.lwt.2026.119060openalex-snapshot
Effective synergistic enzymatic synthesis of theaflavins via combinatorial enzyme screening and system optimization
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114059openalex-snapshot
Enhancement of preference, catalytic activity and thermostability of polyphenol oxidase from Rosa Chinensis by semi-rational engineering
inferred← citeshttps://doi.org/10.1016/j.talanta.2024.126239openalex-snapshot
The enzymatic synthesis of theaflavin-3-gallate oxidation product and its determination
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134457openalex-snapshot
Synthesis of purpurogallin-formic acid ester derivatives and their formation mechanism
inferred← citeshttps://doi.org/10.1016/j.tifs.2024.104755openalex-snapshot
Theaflavins: An underexploited functional compound in black tea
inferred← citeshttps://doi.org/10.1080/07391102.2020.1815584openalex-snapshot
Molecular docking, validation, dynamics simulations, and pharmacokinetic prediction of natural compounds against the SARS-CoV-2 main-protease
inferred← citeshttps://doi.org/10.1111/ijfs.15489openalex-snapshot
In vitro enzymatic synthesis of a monomeric theaflavin using a polyphenol oxidase isozyme from tea ( Camellia sinensis ) leaf
inferred← citeshttps://doi.org/10.65795/f8rm8k88openalex-snapshot
Theaflavin-3,3′-Digallate Encapsulated β-Chitosan Nanoparticles for the Prevention of Chemotherapy-Induced Toxicity: Mechanisms, Therapeutic Potential, and Future Perspectives
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