Pyridazine as a privileged structure: An updated review on anticancer activity of pyridazine containing bioactive molecules
ZX He, YP Gong, X Zhang, LY Ma, W Zhao - European journal of medicinal …, 2021 - Elsevier
Identification of potent anticancer agents with high selectivity and low toxicity remains on the
way to human health. Pyridazine featuring advantageous physicochemical properties and …
way to human health. Pyridazine featuring advantageous physicochemical properties and …
Design, synthesis, and antimicrobial activities of 1, 2, 3-triazole glycoside clickamers
T El Malah, HF Nour, AAE Satti, BA Hemdan… - Molecules, 2020 - mdpi.com
Bacterial resistance remains a significant threat and a leading cause of death worldwide,
despite massive attempts to control infections. In an effort to develop biologically active …
despite massive attempts to control infections. In an effort to develop biologically active …
Synthesis, in vitro antimicrobial evaluation, and molecular docking studies of new isatin-1, 2, 3-triazole hybrids
T El Malah, H Farag, BA Hemdan, REA Mageid… - Journal of Molecular …, 2022 - Elsevier
Antibiotic resistance is rapidly evolving at an alarming rate, posing a severe threat to
humanity. In an effort to develop compounds with antimicrobial activity, we synthesized a …
humanity. In an effort to develop compounds with antimicrobial activity, we synthesized a …
Phthalazone tethered 1, 2, 3-triazole conjugates: In silico molecular docking studies, synthesis, in vitro antiproliferative, and kinase inhibitory activities
Abstract New phthalazone tethered 1, 2, 3-triazole derivatives 12–21 were synthesized
utilizing the Cu (I)-catalyzed click reactions of alkyne-functionalized phthalazone 1 with …
utilizing the Cu (I)-catalyzed click reactions of alkyne-functionalized phthalazone 1 with …
Synthesis and antibiofilm activity of 1, 2, 3-triazole-pyridine hybrids against methicillin-resistant Staphylococcus aureus (MRSA)
T El Malah, HA Soliman, BA Hemdan… - New Journal of …, 2021 - pubs.rsc.org
Antibiotic-resistant bacteria are emerging at an alarming rate, posing a potential threat to
human health. We synthesised alkyne-functionalised pyridines 3 and 4via alkylation of …
human health. We synthesised alkyne-functionalised pyridines 3 and 4via alkylation of …
Benzothiazole-tethered 1, 2, 3-triazoles: synthesis, antimicrobial, antioxidant, and molecular docking studies
T El Malah, MI Hegab, HM Awad… - Journal of Molecular …, 2022 - Elsevier
Over the past decades, antibiotic resistance has garnered considerable attention as a public
health concern. Therefore, it has become necessary to develop new generations of …
health concern. Therefore, it has become necessary to develop new generations of …
Copper (i)-catalysed azide–alkyne cycloaddition and antiproliferative activity of mono-and bis-1, 2, 3-triazole derivatives
T El Malah, REA Mageid, HM Awad… - New Journal of Chemistry, 2020 - pubs.rsc.org
A series of mono-and bis-1, 2, 3-triazole-based molecular architectures were prepared in
excellent yields via the standard copper (I)-catalysed azide–alkyne cycloaddition (CuAAC) …
excellent yields via the standard copper (I)-catalysed azide–alkyne cycloaddition (CuAAC) …
Design, synthesis, molecular docking and antimicrobial activities of novel triazole‐ferulic acid ester hybrid carbohydrates
In spite of search for newer and effective antibacterial drugs, nature has paved way to
identify lead molecules from plants to treat chronic diseases. In an effort to develop …
identify lead molecules from plants to treat chronic diseases. In an effort to develop …
Design and Click Synthesis of Novel 1- Substituted-4-(3,4-Dimethoxyphenyl)-1H-1,2,3-Triazole Hybrids for Anticancer Evaluation and Molecular Docking
T El Malah, H Farag, HM Awad… - Polycyclic Aromatic …, 2023 - Taylor & Francis
In an attempt to improve the performance of biologically active anticancer agents, a novel
series of 1-substituent-4-(3, 4-dimethoxyphenyl)-1 H-1, 2, 3-triazole hybrids 10–16 were …
series of 1-substituent-4-(3, 4-dimethoxyphenyl)-1 H-1, 2, 3-triazole hybrids 10–16 were …
Design, synthesis, and biological evaluation of some new 2-phenyl-3, 6-pyridazinedione derivatives as PDE-5 inhibitors
Abstract Various 2-phenyl-3, 6-pyridazinedione derivatives 4a-j, 5a-c, 6a, b, 7a-c, 8, 9, 10a-
d, and 11a-d, were effectively synthesized, and tested for their potential inhibition of …
d, and 11a-d, were effectively synthesized, and tested for their potential inhibition of …