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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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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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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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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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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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EGCG, green tea polyphenols and their synthetic analogs and prodrugs for human cancer prevention and treatment

Advances in Clinical Chemistry, 2011, Vol.53, p.155-177

2011

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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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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

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

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

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

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

EGCG, green tea polyphenols and their synthetic analogs and prodrugs for human cancer prevention and treatment

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

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