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Thiadiazines

Known as: Thiadiazines [Chemical/Ingredient], thiadiazine 
National Institutes of Health

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29 relations

Narrower (22)

BPDZ 44BPDZ 62BPDZ 79EMD 53986
In Bloodagonistsantagonists & inhibitorsaspects of radiation effects

Broader (1)

nitrogenous heterocyclic compound

Papers overview

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2019
2019
Electrophysiological characterization of a novel AMPA receptor potentiator, TAK-137, in rat hippocampal neurons
2013
2013
Synthesis of new Derivatives of Pyrimido[5,4-e][1,2,4]triazolo[3,4-b] [1,3,4]Thiadiazine and Their Enzyme Inhibitory Activity Assessment on Soybean 15-lipoxygenase
The synthesis of new derivatives of pyrimido[5,4-e][1,2,4]triazolo[3,4-b][1,3,4]thiadiazine is described. These derivatives have… 
Review
2010
Review
2010
Ring-fused thiadiazines as core structures for the development of potent AMPA receptor potentiators.
Amongst ionotropic glutamatergic receptors, the AMPA receptor subtype has been recognized as a major contributor to the fast… 
2008
2008
New Sulphonamide and Carboxamide Derivatives of Acyclic C-Nucleosides of Triazolo-Thiadiazole and the Thiadiazine Analogues. Synthesis, Anti-HIV, and Antitumor Activities. Part 2
A new series of acyclic C-nucleosides 1′,2′-O-isopropylidene-D-ribo-tetritol-1-yl)[1,2,4] triazolo[3,4-b][1,3,4]thiadiazoles… 
2006
2006
Synthesis and anti-HIV evaluation of the novel 2-(m-chlorobenzyl)-4-substituted-7-methyl-1, 1, 3-trioxo-pyrazolo[4, 5-e] [1, 2, 4]thiadiazines
A novel series of 2-(m-Chlorobenzyl)-4-substituted-1, 1, 3-trioxo-2H,4H-pyrazolo[4, 5-e][1, 2, 4] thiadiazines (7a-k) were… 
2004
2004
Fused-ring thiadiazines: preparation and crystallographic characterization of 3-phenyl derivative of benzo-, pyridio[2,3-e]-, pyrazino[2,3-e]-, and tetrafluorobenzo-[1,2,4]thiadiazines.
Four bicyclic 4H-[1,2,4]thiadiazines 1a-d were prepared in 74-88% yields in two steps from the corresponding amidines 2. Three of… 
2001
2001
New thiadiazine derivatives with activity against Trypanosoma cruzi amastigotes.
The cytotoxicity of 18 new 1,2,6-thiadiazin-3,5-dione 1,1-dioxides was evaluated. This group of products was previously assayed… 
2001
2001
PARM: a practical utility for drug design.
2000
2000
Evaluation of drug activity against intracellular forms of Trypanosoma cruzi employing enzyme immunoassay
Objective: To describe application of a new method for the evaluation of anti‐Trypanosoma cruzi activity against intracellular… 
1983
1983
Potential broad spectrum anthelmintics IV: design, synthesis, and antiparasitic screening of certain 3,6-disubstituted-(7H)-s-triazolo-[3,4-b][1,3,4]thiadiazine derivatives.
Abstract A series of 3,6-disubstituted-(7H)-s-triazolo[3,4-b][l,3,4]- thiadiazine derivatives were prepared. The compounds were… 
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