Emilio Parisini

latvian institute of organic synthesis

H指数:33

被引数:4,456

个人简介

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荣誉奖项

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The effect of ionic strength on PETase enzymes: An experimental and computational study

PROTEIN SCIENCE

IF5.2

2025-12-270

OAAI

Mechanistic Insights into Dimerization and Cross-β Sheet Formation in the HIV-Associated Amyloidogenic Peptide PAP248–286 from Unbiased All-Atom Molecular Dynamics Simulations

基于无偏全原子分子动力学模拟的HIV相关淀粉样肽PAP248–286的二聚化及交叉-β片层形成的机制洞察

Computational and Structural Biotechnology Journal

IF4.1

2025-12-160

OAAI

Synthesis; photochemical and biological evaluation of novel photoswitchable glycomimetic ligands of Pseudomonas aeruginosa LecB

合成；新型光控开关糖模拟配体（铜绿假单胞菌LecB）的光化学和生物活性评价

RSC Adv.

IF0

2025-12-130

Development of a highly active engineered PETase enzyme for polyester degradation

一种高效活性工程化PETase酶的开发用于聚酯降解

febs journal

IF0

2025-08-230

OAAI

Functional and Structural Characterization of PETase SM14 from Marine-Sponge Streptomyces sp. Active on Polyethylene Terephthalate

PETase SM14的功能与结构特征：来自海洋海绵链霉菌属（Streptomyces sp.）并作用于聚对苯二甲酸乙二醇酯

ACS SUSTAINABLE CHEMISTRY & ENGINEERING

IF7.3

2025-05-150

PRE

Biological evaluation as antimalarial of two families of biscationic compounds featuring two different sulphur linkers

作为抗疟疾药物的两种具有两种不同硫键合物的双阳离子化合物生物评价

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

IF2.2

2025-04-240

PRE

Discovery of Malarial Threonyl tRNA Synthetase Inhibitors by Screening of a Focused Fragment Library

ACS MEDICINAL CHEMISTRY LETTERS

IF4

2023-12-140

PRE

Tailoring FPOX enzymes for enhanced stability and expanded substrate recognition

SCIENTIFIC REPORTS

IF3.9

2023-10-300

OAAI

Targeting triple-negative breast cancer cells with a 01-integrin binding aptamer

MOLECULAR THERAPY NUCLEIC ACIDS

IF6.1

2023-09-013

OAAI

Light-Based Anti-Biofilm and Antibacterial Strategies

PHARMACEUTICS

IF5.5

2023-08-098

OAAI

New bioisosteric sulphur-containing choline kinase inhibitors with a tracked mode of action

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2023-01-013

PRE

A combined fragment-based virtual screening and STD-NMR approach for the identification of E-cadherin ligands

FRONTIERS IN CHEMISTRY

IF4.2

2022-08-190

OAAI

Recent Approaches to the Identification of Novel Microtubule-Targeting Agents

FRONTIERS IN MOLECULAR BIOSCIENCES

IF4

2022-03-3022

OAAI

Biological Evaluation of New Thienopyridinium and Thienopyrimidinium Derivatives as Human Choline Kinase Inhibitors

PHARMACEUTICS

IF5.5

2022-03-276

OAAI

Anticancer Activity of the Choline Kinase Inhibitor PL48 Is Due to Selective Disruption of Choline Metabolism and Transport Systems in Cancer Cell Lines

PHARMACEUTICS

IF5.5

2022-02-166

OAAI

New Compounds with Bioisosteric Replacement of Classic Choline Kinase Inhibitors Show Potent Antiplasmodial Activity

PHARMACEUTICS

IF5.5

2021-11-022

OAAI

Design, synthesis, biological evaluation and structural characterization of novel GEBR library PDE4D inhibitors

新型GEBR库PDE4D抑制剂的设计、合成、生物学评价及结构表征

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2021-11-0113

PREAI

Hierarchical TiN-Supported TsFDH Nanobiocatalyst for CO2 Reduction to Formate

用于将CO2还原为甲酸盐的分级锡负载TsFDH纳米生物催化剂

CHEMELECTROCHEM

IF3.5

2021-08-0513

OAAI

Rational backbone redesign of a fructosyl peptide oxidase to widen its active site access tunnel

BIOTECHNOLOGY AND BIOENGINEERING

IF3.6

2020-09-0910

PREAI

Insight into GEBR-32a: Chiral Resolution, Absolute Configuration and Enantiopreference in PDE4D Inhibition

洞察GEBR-32a: PDE4D抑制中的手性拆分，绝对构型和对映体参考

MOLECULES

IF4.6

2020-02-1910

OAAI

Emilio Parisini

个人简介

教育背景

工作经历

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