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A Novel IRAK4 Inhibitor DW18134 Ameliorates Peritonitis and Inflammatory Bowel Disease

Molecules (Basel, Switzerland), 2024-04, Vol.29 (8), p.1803

2024

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Synthesis of triazolotriazine derivatives as c-Met inhibitors

Molecular diversity, 2021-05, Vol.25 (2), p.839-846

2021

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Separation of Lycopene via Liquid–Liquid Extraction: An At-Home Experiment in the Kitchen Laboratory

Journal of chemical education, 2024-04, Vol.101 (4), p.1680-1685

2024

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Structural insights into a shared mechanism of human STING activation by a potent agonist and an autoimmune disease-associated mutation

Cell discovery, 2022-12, Vol.8 (1), p.133-133, Article 133

2022

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Preclinical and early clinical studies of a novel compound SYHA1813 that efficiently crosses the blood–brain barrier and exhibits potent activity against glioblastoma

Acta pharmaceutica Sinica. B, 2023-12, Vol.13 (12), p.4748-4764

2023

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Evaluation of Deuterium-Labeled JNJ38877605: Pharmacokinetic, Metabolic, and in Vivo Antitumor Profiles

Chemical research in toxicology, 2018-11, Vol.31 (11), p.1213-1218

2018

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Discovery of pyrrolo[2,3-d]pyrimidine derivatives as potent Axl inhibitors: Design, synthesis and biological evaluation

European journal of medicinal chemistry, 2021-08, Vol.220, p.113497-113497, Article 113497

2021

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Discovery of 10H‑Benzo[b]pyrido[2,3‑e][1,4]oxazine AXL Inhibitors via Structure-Based Drug Design Targeting c‑Met Kinase

Journal of medicinal chemistry, 2023-01, Vol.66 (1), p.220-234

2023

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Design, synthesis, and STING-agonistic activity of benzo[b]thiophene-2-carboxamide derivatives

Molecular diversity, 2023-10

2023

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Discovery of 10 H -Benzo[ b ]pyrido[2,3- e ][1,4]oxazine AXL Inhibitors via Structure-Based Drug Design Targeting c-Met Kinase

Journal of medicinal chemistry, 2023-01, Vol.66 (1), p.220-234

2023

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Discovery of 6-(difluoro(6-(4-fluorophenyl)-[1,2,4]triazolo[4,3-b][1,2,4]triazin-3-yl)methyl)quinoline as a highly potent and selective c-Met inhibitor

European journal of medicinal chemistry, 2016-06, Vol.116, p.239-251

2016

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Discovery of Anilinopyrimidines as Dual Inhibitors of c‑Met and VEGFR-2: Synthesis, SAR, and Cellular Activity

ACS medicinal chemistry letters, 2014-06, Vol.5 (6), p.673-678

2014

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Simm530, a novel and highly selective c-Met inhibitor, blocks c-Met-stimulated signaling and neoplastic activities

Oncotarget, 2016-06, Vol.7 (25), p.38091-38104

2016

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O-Linked Triazolotriazines: Potent and Selective c-Met Inhibitors

ChemMedChem, 2012-07, Vol.7 (7), p.1276-1285

2012

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Abstract B285: A novel, potent, highly selective inhibitor of c-Met kinase, Simm559, inhibits c-Met-dependent neoplastic phenotypes in vitro and in vivo

Molecular cancer therapeutics, 2013-11, Vol.12 (11_Supplement), p.B285-B285

2013

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A highly polymorphic panel of 40-plex microhaplotypes for the Chinese Han population and its application in estimating the number of contributors in DNA mixtures

Forensic science international : genetics, 2022-01, Vol.56, p.102600-102600, Article 102600

2022

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Twenty-five Cases of Adult Prostate Sarcoma Treated at a High-volume Institution From 1989 to 2009

Urology (Ridgewood, N.J.), 2013-07, Vol.82 (1), p.160-165

2013

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Could routine forensic STR genotyping data leak personal phenotypic information?

Forensic science international, 2022-06, Vol.335, p.111311-111311, Article 111311

2022

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Genome‐wide association studies combined with k‐fold cross‐validation identify rs17822931 as an ancestry‐informative marker in Han Chinese population

Electrophoresis, 2023-08, Vol.44 (15-16), p.1187-1196

2023

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Evaluation of a SNP-STR haplotype panel for forensic genotype imputation

Forensic science international : genetics, 2023-01, Vol.62, p.102801-102801, Article 102801

2023

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Guidelines for safe use of Polygoni Multiflori Radix

Acupuncture and herbal medicine, 2024-06, Vol.4 (2), p.151-158

2024

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Phosphorylation of Pirh2 by Calmodulin-dependent kinase II impairs its ability to ubiquitinate p53

The EMBO journal, 2007-07, Vol.26 (13), p.3062-3074

2007

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基于对象存储的新型网络GIS体系结构研究

武汉大学学报（信息科学版）, 2008, Vol.33 (3), p.285-288

喻占武李忠民郑胜

2008

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一种混合式P2P下的大规模地形数据传输机制

测绘学报, 2008, Vol.37 (2), p.243-249

2008

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基于对象存储的海量空间数据存储与管理

武汉大学学报（信息科学版）, 2008, Vol.33 (5), p.528-532

喻占武郑胜李忠民胡滨

2008

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A Novel IRAK4 Inhibitor DW18134 Ameliorates Peritonitis and Inflammatory Bowel Disease

Synthesis of triazolotriazine derivatives as c-Met inhibitors

Separation of Lycopene via Liquid–Liquid Extraction: An At-Home Experiment in the Kitchen Laboratory

Structural insights into a shared mechanism of human STING activation by a potent agonist and an autoimmune disease-associated mutation

Preclinical and early clinical studies of a novel compound SYHA1813 that efficiently crosses the blood–brain barrier and exhibits potent activity against glioblastoma

Evaluation of Deuterium-Labeled JNJ38877605: Pharmacokinetic, Metabolic, and in Vivo Antitumor Profiles

Discovery of pyrrolo[2,3-d]pyrimidine derivatives as potent Axl inhibitors: Design, synthesis and biological evaluation

Discovery of 10H‑Benzo[b]pyrido[2,3‑e][1,4]oxazine AXL Inhibitors via Structure-Based Drug Design Targeting c‑Met Kinase

Design, synthesis, and STING-agonistic activity of benzo[b]thiophene-2-carboxamide derivatives

Discovery of 10 H -Benzo[ b ]pyrido[2,3- e ][1,4]oxazine AXL Inhibitors via Structure-Based Drug Design Targeting c-Met Kinase

Discovery of 6-(difluoro(6-(4-fluorophenyl)-[1,2,4]triazolo[4,3-b][1,2,4]triazin-3-yl)methyl)quinoline as a highly potent and selective c-Met inhibitor

Discovery of Anilinopyrimidines as Dual Inhibitors of c‑Met and VEGFR-2: Synthesis, SAR, and Cellular Activity

Simm530, a novel and highly selective c-Met inhibitor, blocks c-Met-stimulated signaling and neoplastic activities

O-Linked Triazolotriazines: Potent and Selective c-Met Inhibitors

Abstract B285: A novel, potent, highly selective inhibitor of c-Met kinase, Simm559, inhibits c-Met-dependent neoplastic phenotypes in vitro and in vivo

A highly polymorphic panel of 40-plex microhaplotypes for the Chinese Han population and its application in estimating the number of contributors in DNA mixtures

Twenty-five Cases of Adult Prostate Sarcoma Treated at a High-volume Institution From 1989 to 2009

Could routine forensic STR genotyping data leak personal phenotypic information?

Genome‐wide association studies combined with k‐fold cross‐validation identify rs17822931 as an ancestry‐informative marker in Han Chinese population

Evaluation of a SNP-STR haplotype panel for forensic genotype imputation

Guidelines for safe use of Polygoni Multiflori Radix

Phosphorylation of Pirh2 by Calmodulin-dependent kinase II impairs its ability to ubiquitinate p53

基于对象存储的新型网络GIS体系结构研究

一种混合式P2P下的大规模地形数据传输机制

基于对象存储的海量空间数据存储与管理

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