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L

L. Pang

Zhengzhou University

H指数:12

被引数:821

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Pharmacological targeting of the mycothiol cysteine ligase MshC in Mycobacterium abscessus

分枝杆菌脓肿分枝杆菌中麦角硫因半胱氨酸连接酶MshC的药理学靶向

Journal of Biological Chemistry

IF3.9

2026-04-080

OAAI

CuO2 and tannic acid mediated synergistic antimicrobial and antifouling coatings

CuO2和单宁酸介导的协同抗菌和防污涂层

Chemical Engineering Journal

IF13.2

2025-08-220

PRE

Cdc2-like kinases: structure, biological function and therapeutic targets for diseases

Signal Transduction and Targeted Therapy

IF52.7

2023-04-070

OAAI

Partitioning of the initial catalytic steps of leucyl-tRNA synthetase is driven by an active site peptide-plane flip

COMMUNICATIONS BIOLOGY

IF5.1

2022-08-293

OAAI

Detailed resume of RNA m6A demethylases

ACTA PHARMACEUTICA SINICA B

IF14.6

2022-05-0143

OAAI

Synthesis and structure-activity studies of novel anhydrohexitol-based Leucyl-tRNA synthetase inhibitors

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2021-02-0114

OAAI

Synthesis and Biological Evaluation of 1,3-Dideazapurine-Like 7-Amino-5-Hydroxymethyl-Benzimidazole Ribonucleoside Analogues as Aminoacyl-tRNA Synthetase Inhibitors

IF4.6

2020-10-162

OAAI

Synthesis and structural insights into the binding mode of the albomycin δ1 core and its analogues in complex with their target aminoacyl-tRNA synthetase

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2020-09-014

OAAI

Phenyltriazole-functionalized sulfamate inhibitors targeting tyrosyl- or isoleucyl-tRNA synthetase

靶向酪氨酰-或异亮氨酸-tRNA合成酶的苯基三唑官能化氨基磺酸盐抑制剂

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2020-08-0111

OAAI

Structural Insights into the Binding of Natural Pyrimidine-Based Inhibitors of Class II Aminoacyl-tRNA Synthetases

ACS CHEMICAL BIOLOGY

IF3.8

2019-12-2311

OAAI

Synthesis and Biological Evaluation of Lipophilic Nucleoside Analogues as Inhibitors of Aminoacyl-tRNA Synthetases

ANTIBIOTICS-BASEL

IF4.6

2019-10-093

OAAI

Comparative analysis of pyrimidine substituted aminoacyl-sulfamoyl nucleosides as potential inhibitors targeting class I aminoacyl-tRNA synthetases

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2019-07-019

PREAI

Acylated sulfonamide adenosines as potent inhibitors of the adenylate-forming enzyme superfamily

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2019-07-018

OAAI

Family-wide analysis of aminoacyl-sulfamoyl-3-deazaadenosine analogues as inhibitors of aminoacyl-tRNA synthetases

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2018-03-0115

OAAI

Exploration of 1,2,3-triazole-pyrimidine hybrids as potent reversal agents against ABCB1-mediated multidrug resistance

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2018-01-0150

PREAI

LPE-1, an orally active pyrimidine derivative, inhibits growth and mobility of human esophageal cancers by targeting LSD1

PHARMACOLOGICAL RESEARCH

IF10.5

2017-08-0133

PREAI

Design, Synthesis, and Structure-Activity Relationship of Novel LSD1 Inhibitors Based on Pyrimidine-Thiourea Hybrids As Potent, Orally Active Antitumor Agents

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2015-02-06145

PREAI

Design and synthesis of novel 1,2,3-triazole-pyrimidine hybrids as potential anticancer agents

新型1,2，3-三唑嘧啶杂合物作为潜在抗癌药物的设计与合成

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2014-10-01104

PREAI