未登录

R

Renate Griffith

University of Tasmania

H指数:30

被引数:2,445

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Q1291H-CFTR molecular dynamics simulations and ex vivo theratyping in nasal epithelial models and clinical response to elexacaftor/tezacaftor/ivacaftor in a Q1291H/F508del patient

FRONTIERS IN MOLECULAR BIOSCIENCES

IF4

2023-06-011

OAAI

Computational Evaluation of N-Based Transannular Interactions in Some Model Fused Medium-Sized Heterocyclic Systems and Implications for Drug Design

IF4.6

2023-02-083

OAAI

Molecular Dynamics and Theratyping in Airway and Gut Organoids Reveal R352Q-CFTR Conductance Defect

气道和肠道类器官的分子动力学和热异常揭示了R352Q-CFTR电导缺陷

AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY

IF5.3

2022-07-018

OAAI

Discovery of neuroprotective agents that inhibit human prolyl hydroxylase PHD2

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2021-05-015

OAAI

Exploration of the Differences between Amine and Thiolate Addition to Acetylenedicarboxylates

JOURNAL OF ORGANIC CHEMISTRY

IF3.6

2019-10-160

PREAI

Molecular targeting for treatment of human T-lymphotropic virus type 1 infection

分子靶向治疗人类T淋巴病毒1型感染

BIOMEDICINE & PHARMACOTHERAPY

IF7.5

2019-01-0126

OAAI

Design and Synthesis of Lactams Derived from Mucochloric and Mucobromic Acids as Pseudomonas aeruginosa Quorum Sensing Inhibitors

IF4.6

2018-05-0720

OAAI

Development of Potent, Selective SRPK1 Inhibitors as Potential Topical Therapeutics for Neovascular Eye Disease

ACS CHEMICAL BIOLOGY

IF3.8

2017-02-0683

OAAI

Synthesis of antimicrobial glucosamides as bacterial quorum sensing mechanism inhibitors

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2017-02-0116

PREAI

FMS-like tyrosine kinase 3 (FLT3) inhibitors: Molecular docking and experimental studies

EUROPEAN JOURNAL OF PHARMACOLOGY

IF4.7

2016-04-0121

PREAI

From indole to pyrrole, furan, thiophene and pyridine: Search for novel small molecule inhibitors of bacterial transcription initiation complex formation

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2016-03-0120

PREAI

Synthesis and biological activity of novel mono-indole and mono-benzofuran inhibitors of bacterial transcription initiation complex formation

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2015-04-0135

PREAI

Human α1-adrenoceptor subtype selectivity of substituted homobivalent 4-aminoquinolines

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2014-11-011

PREAI

An aspartate in the second extracellular loop of the α1B adrenoceptor regulates agonist binding

EUROPEAN JOURNAL OF PHARMACOLOGY

IF4.7

2014-06-018

PREAI

Stereoselective Fluorination Alters the Geometry of a Cyclic Peptide: Exploration of Backbone-Fluorinated Analogues of Unguisin A

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION

IF16.9

2014-05-2159

OAAI

Synthesis and biological evaluation of 2,5-di(7-indolyl)-1,3, 4-oxadiazoles, and 2-and 7-indolyl 2-(1,3,4-thiadiazolyl)ketones as antimicrobials

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2014-03-0123

PREAI

Development of purely structure-based pharmacophores for the topoisomerase I-DNA-ligand binding pocket

JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN

IF3.1

2013-12-019

OA

Inhibitors of Bacterial Transcription Initiation Complex Formation

ACS CHEMICAL BIOLOGY

IF3.8

2013-07-0561

OA

α1-Adrenoceptor and serotonin 5-HT1A receptor affinity of homobivalent 4-aminoquinoline compounds: An investigation of the effect of linker length

BIOCHEMICAL PHARMACOLOGY

IF5.6

2013-05-017

PREAI

5-HT1A receptor pharmacophores to screen for off-target activity of α1-adrenoceptor antagonists

JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN

IF3.1

2013-04-278

PREAI