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T

Torsten Knieß

Helmholtz-Zentrum Dresden-Rossendorf

H指数:24

被引数:1,695

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Protein phosphatase 2A impairs cardiac uptake of glucose in the mammalian heart

蛋白磷酸酶2A损害哺乳动物心脏中的葡萄糖摄取

Naunyn-Schmiedeberg's Archives of Pharmacology

IF3.1

2026-06-250

OAAI

Cyclotron-Based Production of 67Cu for Radionuclide Theranostics via the 70Zn(p,α)67Cu Reaction

PHARMACEUTICALS

IF4.8

2023-02-1710

OAAI

Exploring Nitric Oxide (NO)-Releasing Celecoxib Derivatives as Modulators of Radioresponse in Pheochromocytoma Cells

IF4.6

2022-10-055

OAAI

Synthesis and Cyclooxygenase Inhibition of Sulfonamide-Substituted (Dihydro)Pyrrolo[3,2,1-hi]indoles and Their Potential Prodrugs

IF4.6

2019-10-2212

OAAI

Nitric Oxide-Releasing Selective Estrogen Receptor Modulators: A Bifunctional Approach to Improve the Therapeutic Index

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2019-05-1714

PREAI

Evaluation of Fluorine-18-Labeled α1(I)-N-Telopeptide Analogs as Substrate-Based Radiotracers for PET Imaging of Melanoma-Associated Lysyl Oxidase

FRONTIERS IN CHEMISTRY

IF4.2

2018-04-267

OAAI

Bridging from Brain to Tumor Imaging: (S)-(-)- and (R)-(+)-[18 F]Fluspidine for Investigation of Sigma-1 Receptors in Tumor-Bearing Mice

IF4.6

2018-03-209

OAAI

Technetium-99m based small molecule radiopharmaceuticals and radiotracers targeting inflammation and infection

DALTON TRANSACTIONS

IF3.3

2017-01-0125

PREAI

Development of Antioxidant COX-2 Inhibitors as Radioprotective Agents for Radiation TherapyA Hypothesis-Driven Review

IF6.6

2016-04-1967

OAAI

18F-Labeled 1,4-Dioxa-8-azaspiro[4.5]decane Derivative: Synthesis and Biological Evaluation of a σ1 Receptor Radioligand with Low Lipophilicity as Potent Tumor Imaging Agent

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2015-07-0223

PREAI

Diaryl-Substituted (Dihydro)pyrrolo[3,2,1-hi]indoles, a Class of Potent COX-2 Inhibitors with Tricyclic Core Structure

JOURNAL OF ORGANIC CHEMISTRY

IF3.6

2015-05-1325

PREAI

Radiolabeled COX-2 Inhibitors for Non-Invasive Visualization of COX-2 Expression and Activity - A Critical Update

IF4.6

2013-05-2972

OAAI

Investigations into the synthesis, radiofluorination and conjugation of a new [18F]fluorocyclobutyl prosthetic group and its in vitro stability using a tyrosine model system

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2013-02-0120

PRE

2-Carbaborane-3-phenyl-1H-indoles-Synthesis via McMurry Reaction and Cyclooxygenase (COX) Inhibition Activity

IF3.4

2013-01-0924

OA

Synthesis, in silico, in vitro, and in vivo investigation of 5-[11C]methoxy-substituted sunitinib, a tyrosine kinase inhibitor of VEGFR-2

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2012-12-0127

PREAI

Radiosynthesis of a 18F-labeled 2,3-diarylsubstituted indole via McMurry coupling for functional characterization of cyclooxygenase-2 (COX-2) in vitro and in vivo

通过McMurry偶联放射合成18f标记的2，3-二芳基取代的吲哚，用于体外和体内cyclooxygenase-2 (COX-2) 的功能表征

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2012-06-0150

PRE

Site-selective radiolabeling of peptides by 18F-fluorobenzoylation with [18F]SFB in solution and on solid phase: a comparative study

IF2.4

2012-02-0140

PREAI

Radiohalogenated 4-anilinoquinazoline-based EGFR-TK inhibitors as potential cancer imaging agents

NUCLEAR MEDICINE AND BIOLOGY

IF3

2012-02-0112

PREAI

Synthesis and radiopharmacological investigation of 3-[4′-[18F]fluorobenzylidene]indolin-2-one as possible tyrosine kinase inhibitor

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2009-11-0121

PRE

Synthesis and cyclooxygenase inhibition of various (aryl-1,2,3-triazole-1-yl)-methanesulfonylphenyl derivatives

各种 (aryl-1，2，3-三唑-1-基)-甲磺酰基苯基衍生物的合成和环氧合酶抑制

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2009-02-0156

PRE