Results 11 to 20 of about 4,025 (222)

Discovery of 3,6-disubstituted pyridazines as a novel class of anticancer agents targeting cyclin-dependent kinase 2: synthesis, biological evaluation and in silico insights

open access: yesJournal of Enzyme Inhibition and Medicinal Chemistry, 2020
Human health in the current medical era is facing numerous challenges, especially cancer. So, the therapeutic arsenal for cancer should be unremittingly enriched with novel small molecules that selectively target tumour cells with minimal toxicity ...
Ahmed Sabt   +6 more
doaj   +2 more sources

Syntheses and Applications of 1,2,3-Triazole-Fused Pyrazines and Pyridazines

open access: yesMolecules, 2022
Pyrazines and pyridazines fused to 1,2,3-triazoles comprise a set of heterocycles obtained through a variety of synthetic routes. Two typical modes of constructing these heterocyclic ring systems are cyclizing a heterocyclic diamine with a nitrite or ...
Gavin R. Hoffman, Allen M. Schoffstall
doaj   +2 more sources

Boron Trifluoride-Mediated Cycloaddition of 3-Bromotetrazine and Silyl Enol Ethers: Synthesis of 3-Bromo-pyridazines [PDF]

open access: yes, 2021
Pyridazines are important scaffolds for medicinal chemistry or crop protection agents, yet the selective preparation of 3-bromo-pyridazines with high regiocontrol remains difficult.
González, Jorge A   +4 more
core   +1 more source

Synthesis and X-ray Crystal Structure Analysis of Substituted 1,2,4-Triazolo [4’,3’:2,3]pyridazino[4,5-b]indole and Its Precursor

open access: yesCrystals, 2023
The hit compound 1,2,4-triazolo[4’,3’:2,3]pyridazino[4,5-b]indole 3 was synthesized from the reflux of 4-amino-5-indolyl-1,2,4-triazole-3-thione 1 with 4′-bromoacetophenone 2 in methanol catalyzed by concentrated HCl and the desired final molecule was ...
Ahmed T. A. Boraei   +5 more
doaj   +1 more source

5,6-Dihydro-[1,2,5]oxadiazolo[3,4-d]pyridazine-4,7-dione

open access: yesMolbank, 2023
1,2,5-Chalcogenadiazoles fused with electron-withdrawing heterocycles have been actively investigated for the preparation of organic photovoltaic materials. [1,2,5]Oxadiazolo[3,4-d]pyridazines are much less studied than other chalcogenadiazolopyridazines
Timofey N. Chmovzh   +2 more
doaj   +1 more source

Hydrazides in the reaction with hydroxypyrrolines: less nucleophilicity – more diversity

open access: yesBeilstein Journal of Organic Chemistry, 2021
Expedient protocols for the synthesis of three types of highly functionalized azaheterocyclic scaffolds (dihydropyridazines, tetrahydropyridazines, and partially saturated tricyclic systems) from readily available hydroxypyrrolines and hydrazides are ...
Dmitrii A. Shabalin   +4 more
doaj   +1 more source

Thiohydrazides in the Synthesis of Functionalized Extranuclear Heterosteroids

open access: yesChemistry Proceedings, 2023
Heterocyclic derivatives of hormones have attracted great interest as a privileged scaffold for drug discovery due to their outstanding biological activity.
Yulia Volkova   +2 more
doaj   +1 more source

PIM KINASES INHIBITORS AND PYRIMIDINE-BASED ANTICANCER AGENTS [PDF]

open access: yesAl-Azhar Journal of Pharmaceutical Sciences, 2023
Human phosphatidyl inositol mannoside kinases (Pim kinases) are important biological target for discovery of new anticancer agents. In addition, Pyrimidines have a good contribution as building blocks of many anticancer agents. Hence, a literature survey
ibrahim issa   +3 more
doaj   +1 more source

A Multifield Study on Dimethyl Acetylenedicarboxylate: A Reagent Able to Build a New Cycle on Diaminoimidazoles

open access: yesMolecules, 2022
A new effective method for the synthesis of imidazo[1,5-b]pyridazines derivatives (yields = 68–89%) by the interaction of 1,2-diamino-4-phenylimidazole with DMAD, in methanol and in the presence of a catalytic amount of acetic acid, is proposed.
Dmitrii Yu. Vandyshev   +8 more
doaj   +1 more source

Pyridazines. IX. Proton Magnetic Resonance Studies of Pyridazine, Pyrazine, and Substituted Pyridazines.

open access: yesChemical and Pharmaceutical Bulletin, 1964
Pyridazine, pyrazine and substituted pyridazines have been studied by proton magnetic resonance spectroscopy. The spectra of pyridazine and pyrazine were analyzed completely with the aid of information obtained from the C13-satellites (in natural isotopic abundance), whereas the spectra of substituted pyridazines were analyzed easily by the usual ...
Tori, Kazuo, Ogata, Masaru
openaire   +3 more sources

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