Results 41 to 50 of about 25,177 (318)

Preparation, structures and preliminary host–guest studies of fluorinated syn-bis-quinoxaline molecular tweezers

open access: yesBeilstein Journal of Organic Chemistry, 2010
A series of polycyclic frameworks with fluorinated syn-facial quinoxaline sidewalls has been prepared as potential molecular tweezers for electron-rich guest compounds.
Markus Etzkorn   +4 more
doaj   +1 more source

Synthesis and Antimicrobial Activity of Some New Quinoxaline Derivatives

open access: yesPharmaceuticals, 2010
2-Chloro-3-methylquinoxaline was selected as a nucleus around which various molecular transformations were performed to obtain new compounds expected to possess optimized antimicrobial activity.
Ram Gopal Singhal   +3 more
doaj   +1 more source

Synthesis of a New Series of Nitrogen/Sulfur Heterocycles by Linking Four Rings: Indole; 1,2,4-Triazole; Pyridazine; and Quinoxaline

open access: yesMolecules, 2020
A new series of nitrogen and sulfur heterocyclic systems were efficiently synthesized by linking the following four rings: indole; 1,2,4-triazole; pyridazine; and quinoxaline hybrids. The strength of the acid that catalyzes the condensation of 4-amino-5-(
Ahmed T. A. Boraei   +3 more
doaj   +1 more source

New substituted quinoxalines inhibit triple-negative breast cancer by specifically downregulating the c-MYC transcription

open access: yesNucleic Acids Research, 2019
Conventional chemotherapy remains the primary treatment option for triple-negative breast cancer (TNBC). However, the current chemotherapeutic drugs have limited effects on TNBC, and often lead to serious side effects as well as drug resistance.
Ming-Hao Hu   +3 more
semanticscholar   +1 more source

Steroidal quinoxalines

open access: yesJournal of Heterocyclic Chemistry, 1973
AbstractThe treatment of 3β‐hydroxy‐16α‐bromo‐5α‐androstan‐17‐one, 3β‐acetoxy‐16α‐bromo‐5‐androsten‐17‐one and 21‐bromo‐5‐pregnen‐3β‐ol‐20‐one with 4,5‐dimethyl‐o‐phenylenediamine gave substituted quinoxalines.Hydrolysis of 3β‐acetoxy‐5‐androsteno[16,17‐b]‐6′,7′‐dimethylquinoxaline produced the corresponding 3β‐hydroxy compound.
openaire   +3 more sources

QuinoxalineTacrine QT78, a Cholinesterase Inhibitor as a Potential Ligand for Alzheimer’s Disease Therapy

open access: yesMolecules, 2019
We report the synthesis and relevant pharmacological properties of the quinoxalinetacrine (QT) hybrid QT78 in a project targeted to identify new non-hepatotoxic tacrine derivatives for Alzheimer’s disease therapy.
Eva Ramos   +11 more
doaj   +1 more source

An Efficient Protocol for the Synthesis of Quinoxaline Derivatives at Room Temperature Using Recyclable Alumina-Supported Heteropolyoxometalates [PDF]

open access: yes, 2012
We report a suitable quinoxaline synthesis using molybdophosphovanadates supported on commercial alumina cylinders as catalysts. These catalysts were prepared by incipient wetness impregnation.
Autino, Juan C.   +4 more
core   +4 more sources

Synthesis of Pyrazines and Quinoxalines via Acceptorless Dehydrogenative Coupling Routes Catalyzed by Manganese Pincer Complexes

open access: yesACS Catalysis, 2018
Base-metal catalyzed dehydrogenative self-coupling of 2-amino alcohols to selectively form functionalized 2,5-substituted pyrazine derivatives is presented.
P. Daw   +5 more
semanticscholar   +1 more source

Quinoxaline:Z′ = 1 form [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2010
A new Z' = 1 crystal structure of quinoxaline (or 1,4-diaza-naphthalene), C(8)H(6)N(2), with one-fifth the volume of the earlier known Z' = 5 structure was obtained by means of an in situ cryocrystallization technique.
Ranganathan, Sathishkumar   +3 more
openaire   +3 more sources

Quinoxaline: A comprehension of current pharmacological advancement in medicinal chemistry

open access: yesEuropean Journal of Medicinal Chemistry Reports, 2022
Quinoxaline is a fused heterocycle ring template present in diverse pharmacophore and widely used in medicinal chemistry. Owing to its vast pharmaceutical profile, several quinoxalines analogous displayed their distinct pharmacological activities. In the
Suresh Kumar Suthar   +4 more
doaj  

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