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NF-IL6, a member of the C/EBP family of transcription factors, binds and trans-activates the human MDR1 gene promoter

The Journal of biological chemistry, 1994-11, Vol.269 (47), p.29715-29719

1994

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Heme prosthetic group required for acetylation of prostaglandin H synthase by aspirin

The FASEB journal, 1989-09, Vol.3 (11), p.2294-2297

1989

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[52] Preparation and proteolytic cleavage of apoprostaglandin endoperoxide synthase

Methods in Enzymology, 1990, Vol.187, p.479-485

1990

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Functional differentiation of cyclooxygenase and peroxidase activities of prostaglandin synthase by trypsin treatment. Possible location of a prosthetic heme binding site

The Journal of biological chemistry, 1988-11, Vol.263 (32), p.16532-16535

1988

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Controlled tryptic digestion of prostaglandin H synthase. Characterization of protein fragments and enhanced rate of proteolysis of oxidatively inactivated enzyme

The Journal of biological chemistry, 1987-12, Vol.262 (35), p.16892-16899

1987

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Preparation and proteolytic cleavage of apoprostaglandin endoperoxide synthases

Methods in enzymology, 1990, Vol.187, p.479-485

1990

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Studies on the structure and function of prostaglandin H synthase

Chen, Ying-Nan Pan

1989

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Gold(I)‐Catalyzed Selective Cyclization and 1,2‐Shift to Prepare Pseudorutaecarpine Derivatives

Advanced synthesis & catalysis, 2022-02, Vol.364 (4), p.787-793

2022

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Comprehensive profiling of 1015 patients’ exomes reveals genomic-clinical associations in colorectal cancer

Nature communications, 2022-04, Vol.13 (1), p.2342-2342, Article 2342

2022

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Synthesis of spiroindolenine-3,3'-pyrrolo[2,1- b ]quinazolinones through gold(I)-catalyzed dearomative cyclization of N -alkynyl quinazolinone-tethered indoles

Organic & biomolecular chemistry, 2022-03, Vol.20 (10), p.2069-2074

2022

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Cryptolepine and aromathecin based mimics as potent G-quadruplex-binding, DNA-cleavage and anticancer agents: Design, synthesis and DNA targeting-induced apoptosis

European journal of medicinal chemistry, 2019-05, Vol.169, p.144-158

2019

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Identification of 3-(benzazol-2-yl)quinoxaline derivatives as potent anticancer compounds: Privileged structure-based design, synthesis, and bioactive evaluation in vitro and in vivo

European journal of medicinal chemistry, 2019-03, Vol.165, p.293-308

2019

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3-(Benzo[ d ]thiazol-2-yl)-4-aminoquinoline derivatives as novel scaffold topoisomerase I inhibitor via DNA intercalation: design, synthesis, and antitumor activities

New journal of chemistry, 2020-07, Vol.44 (26), p.11203-11214

2020

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AMPKα1 confers survival advantage of colorectal cancer cells under metabolic stress by promoting redox balance through the regulation of glutathione reductase phosphorylation

Oncogene, 2020-01, Vol.39 (3), p.637-650

2020

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Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China

American journal of human genetics, 2019-10, Vol.105 (4), p.803-812

2019

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2-Styryl-4-aminoquinazoline derivatives as potent DNA-cleavage, p53-activation and in vivo effective anticancer agents

European journal of medicinal chemistry, 2020-01, Vol.186, p.111851-111851, Article 111851

2020

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Alprostadil liposome microsphere preparation stabilizes vascular plaques and inhibits intra-plaque inflammation

Chinese medical journal, 2012-12, Vol.125 (24), p.4380-4385

2012

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Design and synthesis of luotonin A-derived topoisomerase targeting scaffold with potent antitumor effect and low genotoxicity

Bioorganic chemistry, 2024-02, Vol.143, p.107015-107015, Article 107015

2024

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Design and synthesis of pseudo-rutaecarpines as potent anti-inflammatory agents via regulating MAPK/NF-κB pathways to relieve inflammation-induced acute liver injury in mice

Bioorganic chemistry, 2023-09, Vol.138, p.106611-106611, Article 106611

2023

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Rutaecarpine analogues with potent anti-inflammation to alleviate acute ulcerative colitis via regulating TLR4/MAPK/NF-κB pathway

Results in Chemistry, 2024-01, Vol.7, p.101330, Article 101330

2024

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Germline mutational profile of Chinese patients under 70 years old with colorectal cancer

Cancer communications (London, England), 2020-11, Vol.40 (11), p.620-632

2020

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Symmetry breaking of α-[H2W12O40](6-) depends on the transformation of isopolyoxotungstates

Inorganic chemistry, 2014-05, Vol.53 (10), p.5029-5036

2014

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3-Arylamino-quinoxaline-2-carboxamides inhibit the PI3K/Akt/mTOR signaling pathways to activate P53 and induce apoptosis

Bioorganic chemistry, 2021-09, Vol.114, p.105101-105101, Article 105101

2021

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Substantial transition to clean household energy mix in rural China

National science review, 2022-07, Vol.9 (7), p.nwac050

2022

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Synthesis of spiroindolenine-3,3′-pyrrolo[2,1-]quinazolinones through gold()-catalyzed dearomative cyclization of -alkynyl quinazolinone-tethered indoles

Organic & biomolecular chemistry, 2022-03, Vol.2 (1), p.269-274

2022

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NF-IL6, a member of the C/EBP family of transcription factors, binds and trans-activates the human MDR1 gene promoter

Heme prosthetic group required for acetylation of prostaglandin H synthase by aspirin

[52] Preparation and proteolytic cleavage of apoprostaglandin endoperoxide synthase

Functional differentiation of cyclooxygenase and peroxidase activities of prostaglandin synthase by trypsin treatment. Possible location of a prosthetic heme binding site

Controlled tryptic digestion of prostaglandin H synthase. Characterization of protein fragments and enhanced rate of proteolysis of oxidatively inactivated enzyme

Preparation and proteolytic cleavage of apoprostaglandin endoperoxide synthases

Studies on the structure and function of prostaglandin H synthase

Gold(I)‐Catalyzed Selective Cyclization and 1,2‐Shift to Prepare Pseudorutaecarpine Derivatives

Comprehensive profiling of 1015 patients’ exomes reveals genomic-clinical associations in colorectal cancer

Synthesis of spiroindolenine-3,3'-pyrrolo[2,1- b ]quinazolinones through gold(I)-catalyzed dearomative cyclization of N -alkynyl quinazolinone-tethered indoles

Cryptolepine and aromathecin based mimics as potent G-quadruplex-binding, DNA-cleavage and anticancer agents: Design, synthesis and DNA targeting-induced apoptosis

Identification of 3-(benzazol-2-yl)quinoxaline derivatives as potent anticancer compounds: Privileged structure-based design, synthesis, and bioactive evaluation in vitro and in vivo

3-(Benzo[ d ]thiazol-2-yl)-4-aminoquinoline derivatives as novel scaffold topoisomerase I inhibitor via DNA intercalation: design, synthesis, and antitumor activities

AMPKα1 confers survival advantage of colorectal cancer cells under metabolic stress by promoting redox balance through the regulation of glutathione reductase phosphorylation

Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China

2-Styryl-4-aminoquinazoline derivatives as potent DNA-cleavage, p53-activation and in vivo effective anticancer agents

Alprostadil liposome microsphere preparation stabilizes vascular plaques and inhibits intra-plaque inflammation

Design and synthesis of luotonin A-derived topoisomerase targeting scaffold with potent antitumor effect and low genotoxicity

Design and synthesis of pseudo-rutaecarpines as potent anti-inflammatory agents via regulating MAPK/NF-κB pathways to relieve inflammation-induced acute liver injury in mice

Rutaecarpine analogues with potent anti-inflammation to alleviate acute ulcerative colitis via regulating TLR4/MAPK/NF-κB pathway

Germline mutational profile of Chinese patients under 70 years old with colorectal cancer

Symmetry breaking of α-[H2W12O40](6-) depends on the transformation of isopolyoxotungstates

3-Arylamino-quinoxaline-2-carboxamides inhibit the PI3K/Akt/mTOR signaling pathways to activate P53 and induce apoptosis

Substantial transition to clean household energy mix in rural China

Synthesis of spiroindolenine-3,3′-pyrrolo[2,1-]quinazolinones through gold()-catalyzed dearomative cyclization of -alkynyl quinazolinone-tethered indoles

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