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M

Minghua Cui

Ewha Womans University

H指数:21

被引数:1,494

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Oral nano-formulations for endocrine therapy of endometrioid adenocarcinomas

BIOMEDICINE & PHARMACOTHERAPY

IF7.5

2024-10-010

OAAI

Cordycepin Inhibits Cancer Cell Proliferation and Angiogenesis through a DEK Interaction via ERK Signaling in Cholangiocarcinoma

JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS

IF3.8

2020-05-0121

OAAI

Mortalin contributes to colorectal cancer by promoting proliferation and epithelial-mesenchymal transition

IF3.2

2019-10-2423

OAAI

Discovery of Conformationally Restricted Human Glutaminyl Cyclase Inhibitors as Potent Anti-Alzheimer's Agents by Structure-Based Design

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2019-08-1419

PREAI

Transmembrane 4 L Six Family Member 5 Senses Arginine for mTORC1 Signaling

CELL METABOLISM

IF30.9

2019-06-0150

OAAI

Structure-activity relationship investigation of Phe-Arg mimetic region of human glutaminyl cyclase inhibitors

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2018-07-0118

PREAI

Potent human glutaminyl cyclase inhibitors as potential anti-Alzheimer's agents: Structure-activity relationship study of Arg-mimetic region

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2018-03-0118

PREAI

Inhibitory effect of tartrate against phosphate-induced DJ-1 aggregation

INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES

IF8.5

2018-02-013

PREAI

Expediting the Design, Discovery and Development of Anticancer Drugs using Computational Approaches

CURRENT MEDICINAL CHEMISTRY

IF3.5

2018-01-1131

PREAI

N6-Substituted 5'-N-Methylcarbamoyl-4'-selenoadenosines as Potent and Selective A3 Adenosine Receptor Agonists with Unusual Sugar Puckering and Nucleobase Orientation

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2017-04-1920

OAAI

Discovery of Potent Human Glutaminyl Cyclase Inhibitors as Anti-Alzheimer's Agents Based on Rational Design

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2017-03-1336

PREAI

Synthesis and biological evaluation of 3-substituted 5-benzylidene-1-methyl-2-thiohydantoins as potent NADPH oxidase (NOX) inhibitors

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2016-09-0122

PREAI

Harnessing the Therapeutic Potential of Capsaicin and Its Analogues in Pain and Other Diseases

IF4.6

2016-07-23151

OAAI

Structure activity relationships of benzyl C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonists

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2015-11-017

OAAI

5-Lipoxygenase inhibitors suppress RANKL-induced osteoclast formation via NFATc1 expression

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2015-11-0116

PREAI

The Cell Shape-determining Csd6 Protein from Helicobacter pylori Constitutes a New Family of L,D-Carboxypeptidase

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2015-10-0126

OAAI

A role of 1,25(OH)2D3 supplementation in rats with nonalcoholic steatohepatitis induced by choline-deficient diet

补充1，25(OH)2D3在胆碱缺乏饮食诱导的非酒精性脂肪性肝炎大鼠中的作用

NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES

IF3.7

2015-06-0136

PREAI

Anti-angiogenic activity of thienopyridine derivative LCB03-0110 by targeting VEGFR-2 and JAK/STAT3 Signalling

EXPERIMENTAL DERMATOLOGY

IF3.1

2015-04-2714

PREAI

Transient receptor potential vanilloid type 1 antagonists: a patent review (2011-2014)

EXPERT OPINION ON THERAPEUTIC PATENTS

IF4.6

2015-02-1066

PREAI

Synthesis and Anti-Renal Fibrosis Activity of Conformationally Locked Truncated 2-Hexynyl-N6-Substituted-(N)-Methanocarba-nucleosides as A3 Adenosine Receptor Antagonists and Partial Agonists

构象锁定的截短2-己炔基-n6-取代-(N)-甲烷卡核苷作为A3腺苷受体拮抗剂和部分激动剂的合成和抗肾纤维化活性

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2014-02-0530

OAAI