Nothing Special   »   [go: up one dir, main page]

Hamdy et al., 2021 - Google Patents

New bioactive fused triazolothiadiazoles as Bcl-2-targeted anticancer agents

Hamdy et al., 2021

View HTML
Document ID
9253878708227449206
Author
Hamdy R
Jones A
El-Sadek M
Hamoda A
Shakartalla S
Al Shareef Z
Soliman S
Westwell A
Publication year
Publication venue
International Journal of Molecular Sciences

External Links

Snippet

A series of 3-(6-substituted phenyl-[1, 2, 4]-triazolo [3, 4-b]-[1, 3, 4]-thiadiazol-3-yl)-1H- indoles (5a–l) were designed, synthesized and evaluated for anti-apoptotic Bcl-2-inhibitory activity. Synthesis of the target compounds was readily accomplished through a reaction of …
Continue reading at www.mdpi.com (HTML) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • GPHYSICS
    • G06COMPUTING; CALCULATING; COUNTING
    • G06QDATA PROCESSING SYSTEMS OR METHODS, SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL, SUPERVISORY OR FORECASTING PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL, SUPERVISORY OR FORECASTING PURPOSES, NOT OTHERWISE PROVIDED FOR
    • G06Q50/00Systems or methods specially adapted for a specific business sector, e.g. utilities or tourism
    • G06Q50/10Services
    • G06Q50/22Health care, e.g. hospitals; Social work

Similar Documents

Publication Publication Date Title
Karabacak et al. Synthesis and evaluation of new pyrazoline derivatives as potential anticancer agents
Altıntop et al. Design, synthesis, and biological evaluation of novel 1, 3, 4-thiadiazole derivatives as potential antitumor agents against chronic myelogenous leukemia: Striking effect of nitrothiazole moiety
Hamdy et al. New quinoline-based heterocycles as anticancer agents targeting bcl-2
Alam et al. Synthesis of new 1, 3, 4-oxadiazole-incorporated 1, 2, 3-triazole moieties as potential anticancer agents targeting thymidylate synthase and their docking studies
Pecoraro et al. A new oxadiazole-based topsentin derivative modulates cyclin-dependent kinase 1 expression and exerts cytotoxic effects on pancreatic cancer cells
Kciuk et al. Preparation of novel pyrazolo [4, 3-e] tetrazolo [1, 5-b][1, 2, 4] triazine sulfonamides and their experimental and computational biological studies
Rashdan et al. Synthesis, molecular docking studies and in silico admet screening of new heterocycles linked thiazole conjugates as potent anti-hepatic cancer agents
Wu et al. Design, synthesis, activity and docking study of sorafenib analogs bearing sulfonylurea unit
Hamdy et al. New bioactive fused triazolothiadiazoles as Bcl-2-targeted anticancer agents
Said et al. New 1, 2, 3-Triazole scaffold schiff bases as potential anti-COVID-19: Design, synthesis, DFT-molecular docking, and cytotoxicity aspects
Irfan et al. Exploring the synergistic anticancer potential of benzofuran–oxadiazoles and triazoles: Improved ultrasound-and microwave-assisted synthesis, molecular docking, hemolytic, thrombolytic and anticancer evaluation of furan-based molecules
Shaldam et al. Development of novel quinoline-based sulfonamides as selective cancer-associated carbonic anhydrase isoform IX inhibitors
Wang et al. Discovery of novel bromophenol hybrids as potential anticancer agents through the Ros-mediated apoptotic pathway: Design, synthesis and biological evaluation
Fu et al. Design and antiproliferative evaluation of novel sulfanilamide derivatives as potential tubulin polymerization inhibitors
Hamdy et al. Design, synthesis and evaluation of new bioactive oxadiazole derivatives as anticancer agents targeting bcl-2
Altamimi et al. Synthesis, anticancer screening of some novel trimethoxy quinazolines and VEGFR2, EGFR tyrosine kinase inhibitors assay; molecular docking studies
Al-Ghulikah et al. New pyrimidine-5-carbonitriles as COX-2 inhibitors: design, synthesis, anticancer screening, molecular docking, and in silico ADME profile studies
Alsehli et al. Design and synthesis of benzene homologues tethered with 1, 2, 4-triazole and 1, 3, 4-thiadiazole motifs revealing dual MCF-7/HepG2 cytotoxic activity with prominent selectivity via histone demethylase LSD1 inhibitory effect
Wu et al. Discovery of 2-(4-Substituted-piperidin/piperazine-1-yl)-N-(5-cyclopropyl-1 H-pyrazol-3-yl)-quinazoline-2, 4-diamines as PAK4 Inhibitors with Potent A549 Cell Proliferation, Migration, and Invasion Inhibition Activity
Kartsev et al. Synthesis and antimicrobial activity of new heteroaryl (aryl) thiazole derivatives molecular docking studies
Yousef et al. Design, synthesis, in silico and in vitro studies of new immunomodulatory anticancer nicotinamide derivatives targeting VEGFR-2
Al-Wahaibi et al. Design, synthesis, and antiproliferative activity of new 5-chloro-indole-2-carboxylate and pyrrolo [3, 4-b] indol-3-one derivatives as potent inhibitors of egfrt790m/brafv600e pathways
Abdellattif et al. Oxazinethione derivatives as a precursor to pyrazolone and pyrimidine derivatives: Synthesis, biological activities, molecular modeling, ADME, and molecular dynamics studies
Zajec et al. In Silico Discovery and Optimisation of a Novel Structural Class of Hsp90 C-Terminal Domain Inhibitors
Boichuk et al. Computational-based discovery of the anti-cancer activities of pyrrole-based compounds targeting the colchicine-binding site of tubulin