Z
Zohreh Nazarian
Researcher at Monash University, Clayton campus
Publications - 7
Citations - 126
Zohreh Nazarian is an academic researcher from Monash University, Clayton campus. The author has contributed to research in topics: Biological activity & Reagent. The author has an hindex of 3, co-authored 7 publications receiving 106 citations. Previous affiliations of Zohreh Nazarian include University of Tehran & Tehran University of Medical Sciences.
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Journal ArticleDOI
Chromene-based synthetic chalcones as potent antileishmanial agents: synthesis and biological activity.
Alireza Foroumadi,Saeed Emami,Maedeh Sorkhi,Maryam Nakhjiri,Zohreh Nazarian,Samaneh Heydari,Sussan K. Ardestani,Fatemeh Poorrajab,Abbas Shafiee +8 more
TL;DR: Results from in vitro biological assays indicated that chloro‐substituted 1‐(6‐methoxy‐2H‐chromen‐3‐yl)‐3-phenylpropen‐1‐ones exhibited excellent activity against Leishmania major at non‐cytotoxic concentrations.
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Novel antileishmanial chalconoids: synthesis and biological activity of 1- or 3-(6-chloro-2H-chromen-3-yl)propen-1-ones.
Zohreh Nazarian,Saeed Emami,Samaneh Heydari,Sussan K. Ardestani,Maryam Nakhjiri,Fatemeh Poorrajab,Abbas Shafiee,Alireza Foroumadi +7 more
TL;DR: The results of cytotoxicity assessment against mouse peritoneal macrophage cells showed that these compounds display antileishmanial activity at non-cytotoxic concentrations.
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Synthesis and Cytotoxicity Study of New Cyclopenta[b] quinoline-1,8-dione Derivatives
TL;DR: Although the results of cytotoxic activity evaluation demonstrated that the in-vitro anti-cancer effect of synthesized compounds are mainly low, it seems that this structure can be used as a novel cytotoxicity scaffold for further modification and design of novel potent compounds.
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Double cyclization of O-acylated hydroxyamides generates 1,6-dioxa-3,9-diazaspiro[4.4]nonanes a new class of oxy-oxazolidinones
Zohreh Nazarian,Craig J. Forsyth +1 more
TL;DR: An efficient synthetic route to the synthesis of a new class of oxy-oxazolidinones namely 1,6-dioxa-3,9-diazaspiro[4.4]nonanes via O-acylated α-hydroxyamides by a comparable strategy to the synthesisation of cyclic orthoamides is presented.
Journal ArticleDOI
Novel Antileishmanial Chalconoids: Synthesis and Biological Activity of 1- or 3-(6-Chloro-2H-chromen-3-yl)propen-1-ones.
Zohreh Nazarian,Saeed Emami,Samaneh Heydari,Sussan K. Ardestani,Maryam Nakhjiri,Fatemeh Poorrajab,Abbas Shafiee,Alireza Foroumadi +7 more
TL;DR: A series of chalconoids containing a 6-chloro-2H-chromen-3-yl group were prepared through a convenient and efficient synthetic method by using 5-chloros 2-hydroxybenzaldehyde as starting material as mentioned in this paper.