Maƚgorzata Dukat

virginia commonwealth university school of pharmacy

H指数:30

被引数:2,758

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Stereoselectivity of pleiotropic monoamine transporter 2-benzoylpiperidine inhibitors and their potential application as novel pharmacological tools

多效性单胺转运蛋白2-苯甲酰哌啶抑制剂的立体选择性及其作为新型药理学工具的潜在应用

Biochemical Pharmacology

IF5.6

2026-09-260

PRE

Design of a new psychedelic quipazine analog with therapeutic efficacy and potentially fewer side effects

设计一种具有治疗效果且潜在副作用更少的新型迷幻奎帕嗪类似物

Science Signaling

IF6.6

2026-07-210

PRE

The 2-Amino-3; 4-dihydroquinazoline Molecular Scaffold as Novel OCT3 Inhibitor

2-氨基-3,4-二氢喹唑啉分子骨架作为新型的OCT3抑制剂

ACS Chemical Neuroscience

IF3.9

2026-03-190

Dual Modulation of 5-HT2A Receptors and SERT by α-Ethyltryptamine and Its Optical Isomers

α-乙基色胺及其光学异构体对5-HT2A受体和SERT的联合调节

ACS CHEMICAL NEUROSCIENCE

IF3.9

2025-12-010

PRE

Pharmacological Characterization of a-Ethyltryptamine-based 5-HT2A Receptor Agonists for Therapeutic Use

基于α-乙基色胺的5-HT2A受体激动剂的药理学特性及其治疗应用

JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS

IF3.8

2025-03-010

PRE

Discriminative stimulus properties of α-ethyltryptamine (α-ET) in rats: α-ET-like effects of MDMA, MDA and aryl-monomethoxy substituted derivatives of α-ET

PSYCHOPHARMACOLOGY

IF3.3

2024-12-280

PRE

Do 2-(Benzoyl)piperidines Represent a Novel Class of hDAT Reuptake Inhibitors?

ACS CHEMICAL NEUROSCIENCE

IF3.9

2023-02-062

PRE

N1H- and N1-Substituted Phenylguanidines as α7 Nicotinic Acetylcholine (nACh) Receptor Antagonists: Structure-Activity Relationship Studies

ACS CHEMICAL NEUROSCIENCE

IF3.9

2021-05-272

PREAI

Psychedelic-like Properties of Quipazine and Its Structural Analogues in Mice

ACS CHEMICAL NEUROSCIENCE

IF3.9

2021-01-0515

X-ray crystal structure of a 2-amino-3,4-dihydroquinazoline 5-HT3 serotonin receptor antagonist and related analogs

JOURNAL OF MOLECULAR STRUCTURE

IF4.7

2020-02-010

OAAI

Multi-modal antidepressant-like action of 6-and 7-chloro-2-aminodihydroquinazolines in the mouse tail suspension test

PSYCHOPHARMACOLOGY

IF3.3

2019-02-2511

OAAI

Revised Pharmacophore Model for 5-HT2A Receptor Antagonists Derived from the Atypical Antipsychotic Agent Risperidone

ACS CHEMICAL NEUROSCIENCE

IF3.9

2019-01-0413

PREAI

Methylene Bridge to 5-HT3 Receptor Antagonists: Conformationally Constrained Phenylguanidines

ACS CHEMICAL NEUROSCIENCE

IF3.9

2018-10-303

PREAI

des-Formylflustrabronnine (dFBr): A Structure-Activity Study on Its Ability To Potentiate the Action of Acetylcholine at α4β2 Nicotinic Acetylcholine Receptors

ACS CHEMICAL NEUROSCIENCE

IF3.9

2018-07-208

PREAI

Superagonist, Full Agonist, Partial Agonist, and Antagonist Actions of Arylguanidines at 5-Hydroxytryptamine-3 (5-HT3) Subunit A Receptors

ACS CHEMICAL NEUROSCIENCE

IF3.9

2016-09-0610

PREAI

Reformulating a Pharmacophore for 5-HT2A Serotonin Receptor Antagonists

ACS CHEMICAL NEUROSCIENCE

IF3.9

2016-07-1910

OAAI

Deconstruction of the α4β2 Nicotinic Acetylcholine Receptor Positive Allosteric Modulator Desformylflustrabromine

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2011-10-0322

Toward Selective Drug Development for the Human 5-Hydroxytryptamine 1E Receptor: A Comparison of 5-Hydroxytryptamine 1E and 1F Receptor Structure-Affinity Relationships

JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS

IF3.8

2011-06-0122

OAAI

MD-354 selectively antagonizes the antinociceptive effects of (-)nicotine in the mouse tail-flick assay

MD-354在小鼠甩尾试验中选择性拮抗 (-) 尼古丁的镇痛作用

PSYCHOPHARMACOLOGY

IF3.3

2010-04-306

PREAI

Binding of serotonin and N1-benzenesulfonyltryptamine-related analogs at human 5-HT6 serotonin receptors:: Receptor modeling studies

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2008-01-1837

Maƚgorzata Dukat

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