Raphael Rahmani

Parkville, VIC 3052, Australia

Last Updated: 09/26/2026

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Found 16 publications

Heterocyclic core modifications in trypanosomacidal 2-[(phenylheteroaryl)ethyl]ureas.

Heterocyclic core modifications in trypanosomacidal 2-[(phenylheteroaryl)ethyl]ureas.

Journal: RSC medicinal chemistry

Published: October 01, 2024

Novel aroyl guanidine anti-trypanosomal compounds that exert opposing effects on parasite energy metabolism.

Novel aroyl guanidine anti-trypanosomal compounds that exert opposing effects on parasite energy metabolism.

Journal: European journal of medicinal chemistry

Published: November 07, 2023

Structure-Activity Studies of Truncated Latrunculin Analogues with Antimalarial Activity.

Structure-Activity Studies of Truncated Latrunculin Analogues with Antimalarial Activity.

Journal: ChemMedChem

Published: June 08, 2020

Hit-to-lead optimization of novel benzimidazole phenylacetamides as broad spectrum trypanosomacides.

Hit-to-lead optimization of novel benzimidazole phenylacetamides as broad spectrum trypanosomacides.

Journal: RSC medicinal chemistry

Published: February 21, 2020

Crystal structure of the M5 muscarinic acetylcholine receptor.

Crystal structure of the M5 muscarinic acetylcholine receptor.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: November 28, 2019

Discovery of Potent N-Ethylurea Pyrazole Derivatives as Dual Inhibitors of Trypanosoma brucei and Trypanosoma cruzi.

Discovery of Potent N-Ethylurea Pyrazole Derivatives as Dual Inhibitors of Trypanosoma brucei and Trypanosoma cruzi.

Journal: ACS medicinal chemistry letters

Published: May 29, 2019

8-Mercaptoguanine Derivatives as Inhibitors of Dihydropteroate Synthase.

8-Mercaptoguanine Derivatives as Inhibitors of Dihydropteroate Synthase.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: October 06, 2017

Truncated Latrunculins as Actin Inhibitors Targeting Plasmodium falciparum Motility and Host Cell Invasion.

Truncated Latrunculins as Actin Inhibitors Targeting Plasmodium falciparum Motility and Host Cell Invasion.

Journal: Journal of medicinal chemistry

Published: December 23, 2016

Hit-to-Lead Optimization of a Novel Class of Potent, Broad-Spectrum Trypanosomacides.

Hit-to-Lead Optimization of a Novel Class of Potent, Broad-Spectrum Trypanosomacides.

Journal: Journal of medicinal chemistry

Published: August 23, 2016

Structural Basis for the Selective Binding of Inhibitors to 6-Hydroxymethyl-7,8-dihydropterin Pyrophosphokinase from Staphylococcus aureus and Escherichia coli.

Structural Basis for the Selective Binding of Inhibitors to 6-Hydroxymethyl-7,8-dihydropterin Pyrophosphokinase from Staphylococcus aureus and Escherichia coli.

Journal: Journal of medicinal chemistry

Published: April 21, 2016

6-Arylpyrazine-2-carboxamides: A New Core for Trypanosoma brucei Inhibitors.

6-Arylpyrazine-2-carboxamides: A New Core for Trypanosoma brucei Inhibitors.

Journal: Journal of medicinal chemistry

Published: August 07, 2015

Structure-based design and development of functionalized Mercaptoguanine derivatives as inhibitors of the folate biosynthesis pathway enzyme 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase from Staphylococcus aureus.

Structure-based design and development of functionalized Mercaptoguanine derivatives as inhibitors of the folate biosynthesis pathway enzyme 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase from Staphylococcus aureus.

Journal: Journal of medicinal chemistry

Published: October 31, 2014

Showing 1-12 of 16

Last Updated: 09/26/2026