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O -Sulfation disposition of curcumin and quercetin in SULT1A3 overexpressing HEK293 cells: the role of arylsulfatase B in cellular O -sulfation regulated by transporters

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What this work says

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

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Sulfatases: Structure, Mechanism, Biological Activity, Inhibition, and Synthetic Utility

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The liver–gut microbiota axis modulates hepatotoxicity of tacrine in the rat

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Resveratrol and its major sulfated conjugates are substrates of organic anion transporting polypeptides (OATPs): Impact on growth of ZR‐75‐1 breast cancer cells

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Sulfonation of curcuminoids: Characterization and contribution of individual SULT enzymes

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Human sulfatases: A structural perspective to catalysis

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Inhibition of multidrug resistance proteins MRP1 and MRP2 by a series of α,β-unsaturated carbonyl compounds

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Sulfation of melatonin: Enzymatic characterization, differences of organs, species and genders, and bioactivity variation

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MK571 inhibits phase-2 conjugation of flavonols by Caco-2/TC7 cells, but does not specifically inhibit their apical efflux

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Efflux transport of chrysin and apigenin sulfates in HEK293 cells overexpressing SULT1A3: The role of multidrug resistance-associated protein 4 (MRP4/ABCC4)

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Phytochemical mediated-modulation of the expression and transporter function of breast cancer resistance protein at the blood-brain barrier: An in-vitro study

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Identification and quantitation of enzyme and transporter contributions to hepatic clearance for the assessment of potential drug-drug interactions

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Sulfation disposition of liquiritigenin in SULT1A3 overexpressing HEK293 cells: The role of breast cancer resistance protein (BCRP) and multidrug resistance-associated protein 4 (MRP4) in sulfate efflux of liquiritigenin

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Multidrug resistance-associated protein 2 (MRP2) is an efflux transporter of EGCG and its metabolites in the human small intestine

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Quantitative prediction of pharmacokinetic properties of drugs in humans: Recent advance in in vitro models to predict the impact of efflux transporters in the small intestine and blood–brain barrier

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Metabolism of quercetin-7- and quercetin-3-glucuronides by an in vitro hepatic model: the role of human β-glucuronidase, sulfotransferase, catechol-O-methyltransferase and multi-resistant protein 2 (MRP2) in flavonoid metabolism

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Genistein inhibits glucose and sulphate transport in isolated rat liver lysosomes

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Decreased Expression of Multidrug Resistance-Associated Protein 4 (MRP4/ABCC4) Leads to Reduced Glucuronidation of Flavonoids in UGT1A1-Overexpressing HeLa Cells: The Role of Futile Recycling

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Bioavailability of Curcumin: Problems and Promises

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Identification of 14 Quercetin Phase II Mono- and Mixed Conjugates and Their Formation by Rat and Human Phase II in Vitro Model Systems

inferredcites →https://doi.org/10.1038/nprot.2014.173openalex-snapshot

Screening and large-scale expression of membrane proteins in mammalian cells for structural studies

inferredcites →https://doi.org/10.1039/c2fo10254dopenalex-snapshot

Quercetin increased bioavailability and decreased methylation of green tea polyphenols in vitro and in vivo

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Mutual interactions between flavonoids and enzymatic and transporter elements responsible for flavonoid disposition via phase II metabolic pathways

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Phenolic compounds: current industrial applications, limitations and future challenges

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Lysosomal sulfatases: a growing family

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Influence of Piperine on the Pharmacokinetics of Curcumin in Animals and Human Volunteers

inferredcites →https://doi.org/10.1080/09168451.2016.1222266openalex-snapshot

Updated perspectives on the cytosolic sulfotransferases (SULTs) and SULT-mediated sulfation

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Human metabolism of dietary flavonoids: Identification of plasma metabolites of quercetin

inferredcites →https://doi.org/10.1080/17425255.2020.1732348openalex-snapshot

Transcription factor-mediated regulation of the BCRP/ ABCG2 efflux transporter: a review across tissues and species

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Cancer-derived cholesterol sulfate is a key mediator to prevent tumor infiltration by effector T cells

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Phytochemicals Induce Breast Cancer Resistance Protein in Caco-2 Cells and Enhance the Transport of Benzo[a]pyrene-3-sulfate

inferredcites →https://doi.org/10.1111/nyas.13384openalex-snapshot

Flavonoids as modulators of metabolic enzymes and drug transporters

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Involvement of Breast Cancer Resistance Protein (BCRP/ABCG2) in the Biliary Excretion and Intestinal Efflux of Troglitazone Sulfate, the Major Metabolite of Troglitazone with a Cholestatic Effect

inferredcites →https://doi.org/10.1124/dmd.113.050930openalex-snapshot

Downregulation of Sulfotransferase Expression and Activity in Diseased Human Livers

inferredcites →https://doi.org/10.1124/dmd.115.065953openalex-snapshot

Multidrug Resistance-Associated Protein 4 (MRP4/ABCC4) Controls Efflux Transport of Hesperetin Sulfates in Sulfotransferase 1A3–Overexpressing Human Embryonic Kidney 293 Cells

inferredcites →https://doi.org/10.1124/dmd.116.070938openalex-snapshot

Arylsulfatase B Mediates the Sulfonation-Transport Interplay in Human Embryonic Kidney 293 Cells Overexpressing Sulfotransferase 1A3

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Leveraging of Rifampicin-Dosed Cynomolgus Monkeys to Identify Bile Acid 3-O-Sulfate Conjugates as Potential Novel Biomarkers for Organic Anion-Transporting Polypeptides

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Hepatic Transport of 25-Hydroxyvitamin D3 Conjugates: A Mechanism of 25-Hydroxyvitamin D3 Delivery to the Intestinal Tract

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Curcumin as an In Vivo Selective Intestinal Breast Cancer Resistance Protein Inhibitor in Cynomolgus Monkeys

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Developmental Expression of the Cytosolic Sulfotransferases in Human Liver

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The Role of Sulfotransferases in Liver Diseases

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Effects of Chrysin and Its Major Conjugated Metabolites Chrysin-7-Sulfate and Chrysin-7-Glucuronide on Cytochrome P450 Enzymes and on OATP, P-gp, BCRP, and MRP2 Transporters

inferredcites →https://doi.org/10.1124/dmd.121.000430openalex-snapshot

Comparative Hepatic and Intestinal Efflux Transport of Statins

inferredcites →https://doi.org/10.1124/dmd.121.000478openalex-snapshot

From Steroid and Drug Metabolism to Glycobiology, Using Sulfotransferase Structures to Understand and Tailor Function

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Metabolism of Flavonoids via Enteric Recycling: Mechanistic Studies of Disposition of Apigenin in the Caco-2 Cell Culture Model

inferredcites →https://doi.org/10.1177/2472555219867070openalex-snapshot

Functional Expression of Multidrug Resistance Protein 4 MRP4/ABCC4

inferredcites →https://doi.org/10.1208/s12248-014-9668-6openalex-snapshot

Role of the Breast Cancer Resistance Protein (BCRP/ABCG2) in Drug Transport—an Update

inferredcites →https://doi.org/10.1210/er.2015-1036openalex-snapshot

The Regulation of Steroid Action by Sulfation and Desulfation

inferredcites →https://doi.org/10.2174/1389201019666180308091855openalex-snapshot

Evaluation of Drug Transport in MDCKII-Wild Type, MDCKII-MDR1, MDCKII-BCRP and Caco-2 Cell Lines

inferredcites →https://doi.org/10.3109/09687688.2012.703703openalex-snapshot

Overexpression of membrane proteins in mammalian cells for structural studies

inferredcites →https://doi.org/10.33549/physiolres.933160openalex-snapshot

Reduced Sulfotransferase SULT2A1 Activity in Patients With Alzheimer´s Disease

inferredcites →https://doi.org/10.3389/fphar.2020.614756openalex-snapshot

Characterization of Formononetin Sulfonation in SULT1A3 Overexpressing HKE293 Cells: Involvement of Multidrug Resistance-Associated Protein 4 in Excretion of Sulfate

inferredcites →https://doi.org/10.3389/fphar.2021.802539openalex-snapshot

The Role of Uptake and Efflux Transporters in the Disposition of Glucuronide and Sulfate Conjugates

inferredcites →https://doi.org/10.3390/ijms18112231openalex-snapshot

Chemoenzymatic Preparation and Biophysical Properties of Sulfated Quercetin Metabolites

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Inhibitory Effects of Quercetin and Its Main Methyl, Sulfate, and Glucuronic Acid Conjugates on Cytochrome P450 Enzymes, and on OATP, BCRP and MRP2 Transporters

inferredcites →https://doi.org/10.3390/pharmaceutics12050397openalex-snapshot

Quercetin Is a Flavonoid Breast Cancer Resistance Protein Inhibitor with an Impact on the Oral Pharmacokinetics of Sulfasalazine in Rats

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Negligible Effect of Quercetin in the Pharmacokinetics of Sulfasalazine in Rats and Beagles: Metabolic Inactivation of the Interaction Potential of Quercetin with BCRP

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Incoming claims: where this work appears in other papers’ reference lists and arguments.

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A critical examination of human data for the biological activity of quercetin and its phase-2 conjugates

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Farnesoid X receptor represses human sulfotransferase 1A3 expression through direct binding to the promoter

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