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SphK2 confers 5-fluorouracil resistance to colorectal cancer via upregulating H3K56ac-mediated DPD expression

Oncogene, 2020-07, Vol.39 (29), p.5214-5227

2020

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Increased S1P induces S1PR2 internalization to blunt the sensitivity of colorectal cancer to 5-fluorouracil via promoting intracellular uracil generation

Acta pharmacologica Sinica, 2021-03, Vol.42 (3), p.460-469

2021

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Synthesis of methylated quercetin derivatives and their reversal activities on P-gp- and BCRP-mediated multidrug resistance tumour cells

European journal of medicinal chemistry, 2012-08, Vol.54, p.413-422

2012

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Structural modification of oridonin via DAST induced rearrangement

RSC advances, 2018-01, Vol.8 (52), p.29548-29554

2018

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Organocatalytic asymmetric synthesis of both cis - and trans -configured pyrano[2,3- b ]chromenes via different dehydration pathways

Organic Chemistry Frontiers, 2019-06, Vol.6 (12), p.1972-1976

2019

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S1PR2 inhibitors potently reverse 5-FU resistance by downregulating DPD expression in colorectal cancer

Pharmacological research, 2020-05, Vol.155, p.104717, Article 104717

2020

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Synthesis and evaluation of stereoisomers of methylated catechin and epigallocatechin derivatives on modulating P-glycoprotein-mediated multidrug resistance in cancers

European journal of medicinal chemistry, 2021-12, Vol.226, p.113795, Article 113795

2021

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Potent and Nontoxic Chemosensitizer of P‑Glycoprotein-Mediated Multidrug Resistance in Cancer: Synthesis and Evaluation of Methylated Epigallocatechin, Gallocatechin, and Dihydromyricetin Derivatives

Journal of medicinal chemistry, 2015-06, Vol.58 (11), p.4529-4549

2015

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Novel α-Lipoic Acid/3- n -Butylphthalide Conjugate Enhances Protective Effects against Oxidative Stress and 6-OHDA Induced Neuronal Damage

ACS chemical neuroscience, 2020-06, Vol.11 (11), p.1634-1642

2020

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First total synthesis of marine alkaloid hyrtiosulawesine

Chinese chemical letters, 2010-11, Vol.21 (11), p.1307-1309

2010

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First preparation of a novel polyol resin for purifying arylboronic acids

Chinese chemical letters, 2012-09, Vol.23 (9), p.993-995

2012

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Prodrugs of fluoro-substituted benzoates of EGC as tumor cellular proteasome inhibitors and apoptosis inducers

International journal of molecular sciences, 2008-06, Vol.9 (6), p.951-961

2008

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Facile synthesis of a 4-anilinoquinazoline dimer by Suzuki cross-coupling reaction

Chinese chemical letters, 2011-09, Vol.22 (9), p.1033-1035

2011

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First total synthesis of eudistalbin A

Chinese chemical letters, 2010-08, Vol.21 (8), p.889-891

2010

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Methylation suppresses the proteasome-inhibitory function of green tea polyphenols

Journal of cellular physiology, 2007-10, Vol.213 (1), p.252-260

2007

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Antitumor activity of novel fluoro-substituted (–)-epigallocatechin-3-gallate analogs

Cancer letters, 2010-06, Vol.292 (1), p.48-53

2010

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Modification of marine natural product ningalin B and SAR study lead to potent P-glycoprotein inhibitors

Marine drugs, 2014-10, Vol.12 (10), p.5209-5221

2014

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Study of the green tea polyphenols catechin-3-gallate (CG) and epicatechin-3-gallate (ECG) as proteasome inhibitors

Bioorganic & medicinal chemistry, 2004-07, Vol.12 (13), p.3521-3527

2004

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Regiospecific and enantioselective synthesis of methylated metabolites of tea catechins

Tetrahedron, 2006-06, Vol.62 (25), p.5897-5904

2006

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Enantioselective synthesis of afzelechin and epiafzelechin

Tetrahedron, 2004-09, Vol.60 (37), p.8207-8211

2004

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Semisynthesis of Fluoro-substituted Benzoates of Epi-gallocatechin

Synthetic communications, 2012-12, Vol.42 (23), p.3524-3531

2012

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Structure–activity study of epi-gallocatechin gallate (EGCG) analogs as proteasome inhibitors

Bioorganic & medicinal chemistry, 2005-03, Vol.13 (6), p.2177-2185

2005

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An experimental study of the cervical lymphatic imaging in interstitial magnetic resonance lymphography of tongue using Dextran-DTPA-Gd

Shanghai kou qiang yi xue, 2012-06, Vol.21 (3), p.283

2012

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Study of the green tea polyphenols catechin-3-gallate (CG) and epicatechin-3-gallate (ECG) as proteasome inhibitors

Bioorganic & medicinal chemistry, 2004-07, Vol.12 (13), p.3521-3527

2004

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Corrigendum to “S1PR2 inhibitors potently reverse 5-FU resistance by downregulating DPD expression in colorectal cancer” [Pharmacol Res. 155 (2020) 104717]

Pharmacological research, 2020-09, Vol.159, p.104834-104834, Article 104834

2020

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SphK2 confers 5-fluorouracil resistance to colorectal cancer via upregulating H3K56ac-mediated DPD expression

Increased S1P induces S1PR2 internalization to blunt the sensitivity of colorectal cancer to 5-fluorouracil via promoting intracellular uracil generation

Synthesis of methylated quercetin derivatives and their reversal activities on P-gp- and BCRP-mediated multidrug resistance tumour cells

Structural modification of oridonin via DAST induced rearrangement

Organocatalytic asymmetric synthesis of both cis - and trans -configured pyrano[2,3- b ]chromenes via different dehydration pathways

S1PR2 inhibitors potently reverse 5-FU resistance by downregulating DPD expression in colorectal cancer

Synthesis and evaluation of stereoisomers of methylated catechin and epigallocatechin derivatives on modulating P-glycoprotein-mediated multidrug resistance in cancers

Potent and Nontoxic Chemosensitizer of P‑Glycoprotein-Mediated Multidrug Resistance in Cancer: Synthesis and Evaluation of Methylated Epigallocatechin, Gallocatechin, and Dihydromyricetin Derivatives

Novel α-Lipoic Acid/3- n -Butylphthalide Conjugate Enhances Protective Effects against Oxidative Stress and 6-OHDA Induced Neuronal Damage

First total synthesis of marine alkaloid hyrtiosulawesine

First preparation of a novel polyol resin for purifying arylboronic acids

Prodrugs of fluoro-substituted benzoates of EGC as tumor cellular proteasome inhibitors and apoptosis inducers

Facile synthesis of a 4-anilinoquinazoline dimer by Suzuki cross-coupling reaction

First total synthesis of eudistalbin A

Methylation suppresses the proteasome-inhibitory function of green tea polyphenols

Antitumor activity of novel fluoro-substituted (–)-epigallocatechin-3-gallate analogs

Modification of marine natural product ningalin B and SAR study lead to potent P-glycoprotein inhibitors

Study of the green tea polyphenols catechin-3-gallate (CG) and epicatechin-3-gallate (ECG) as proteasome inhibitors

Regiospecific and enantioselective synthesis of methylated metabolites of tea catechins

Enantioselective synthesis of afzelechin and epiafzelechin

Semisynthesis of Fluoro-substituted Benzoates of Epi-gallocatechin

Structure–activity study of epi-gallocatechin gallate (EGCG) analogs as proteasome inhibitors

An experimental study of the cervical lymphatic imaging in interstitial magnetic resonance lymphography of tongue using Dextran-DTPA-Gd

Study of the green tea polyphenols catechin-3-gallate (CG) and epicatechin-3-gallate (ECG) as proteasome inhibitors

Corrigendum to “S1PR2 inhibitors potently reverse 5-FU resistance by downregulating DPD expression in colorectal cancer” [Pharmacol Res. 155 (2020) 104717]

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