P
Parviz Rashidi Ranjbar
Researcher at University of Tehran
Publications - 47
Citations - 518
Parviz Rashidi Ranjbar is an academic researcher from University of Tehran. The author has contributed to research in topics: Catalysis & One-pot synthesis. The author has an hindex of 11, co-authored 44 publications receiving 356 citations. Previous affiliations of Parviz Rashidi Ranjbar include Hobart Corporation.
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Journal ArticleDOI
Biscoumarin-1,2,3-triazole hybrids as novel anti-diabetic agents: Design, synthesis, in vitro α-glucosidase inhibition, kinetic, and docking studies.
Mohammad Sadegh Asgari,Maryam Mohammadi-Khanaposhtani,Mitra Kiani,Parviz Rashidi Ranjbar,Ebrahim Zabihi,Roghayeh Pourbagher,Rahmatollah Rahimi,Mohammad Ali Faramarzi,Mahmood Biglar,Bagher Larijani,Mohammad Mahdavi,Haleh Hamedifar,Mir Hamed Hajimiri +12 more
TL;DR: Kinetic study revealed that compound 6c inhibits the α-glucosidase in a competitive mode and molecular docking investigation was performed to find interaction modes of the biscoumarin-1,2,3-triazole derivatives.
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Design, synthesis and in vitro α-glucosidase inhibition of novel dihydropyrano[3,2-c]quinoline derivatives as potential anti-diabetic agents.
Hamideh Nikookar,Maryam Mohammadi-Khanaposhtani,Somaye Imanparast,Mohammad Ali Faramarzi,Parviz Rashidi Ranjbar,Mohammad Mahdavi,Bagher Larijani +6 more
TL;DR: A novel series of dihydropyrano[3,2-c]quinoline derivatives 6a-q were synthesized and evaluated for their in vitro α-glucosidase inhibitory activities and the cytotoxicity of the most potent compounds were evaluated using breast cancer cell lines by using a MTT assay, and no toxicity was observed.
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Novel quinazolin-4(3H)-one linked to 1,2,3-triazoles: Synthesis and anticancer activity
Maliheh Safavi,Arsalan Ashtari,Faezeh Khalili,Seyedeh Sara Mirfazli,Mina Saeedi,Sussan Kabudanian Ardestani,Parviz Rashidi Ranjbar,Maliheh Barazandeh Tehrani,Bagher Larijani,Mohammad Mahdavi +9 more
TL;DR: The results revealed that the anticancer activity of the synthesized compounds was selectively affected by the presence of methoxy group on the linker between quinazolinone and 1,2,3‐triazole moieties.
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Copper supported β-cyclodextrin grafted magnetic nanoparticles as an efficient recyclable catalyst for one-pot synthesis of 1-benzyl-1H-1,2,3-triazoldibenzodiazepinone derivatives via click reaction
Mohammad Mahdavi,Hosein Lijan,Saeed Bahadorikhalili,Leila Ma’mani,Parviz Rashidi Ranjbar,Abbas Shafiee +5 more
TL;DR: An efficient and recoverable copper catalyst was prepared by the immobilization of Cu into β-cyclodextrin covalently attached to magnetic nanoparticles (denoted as [Cu@β-CD@SPIONs) as discussed by the authors ).
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One-Pot, Four-Component Synthesis of Novel Imidazo[2,1-b]thiazol-5-amine Derivatives
Mohammad Mahdavi,Mehdi Asadi,Mina Saeedi,Mostafa Ebrahimi,Mohammad Ali Rasouli,Parviz Rashidi Ranjbar,Alireza Foroumadi,Abbas Shafiee +7 more
TL;DR: In this article, a novel imidazo[2,1-b]thiazol-5-amine derivatives were synthesized by a one-pot, four-component reaction of 2-bromoacetophenone derivatives, aromatic aldehydes, thiourea, and isocyanides under reflux conditions.