Results 191 to 200 of about 49,222 (248)

Enhancement of gemcitabine toxicity and specificity through PI3K/Akt/Nrf2 pathway inhibition in pancreatic cancer. [PDF]

Front Pharmacol
Chen YS, O'Hagan S, Day PJR.
europepmc   +1 more source

Nickel Thiazoledithiolenes: π-Extended Fused-Ring Metal Dithiolenes as Highly Delocalized π-Electron Systems with Stabilized Frontier Orbitals. [PDF]

Molecules
Uzelac EJ, Sánchez-Rincón J, Ruiz Delgado MC, Rasmussen SC.   +3 more
europepmc   +1 more source

Thiazole-carboxamide derivatives as potent antioxidant agents with drug-like properties: In vitro, molecular docking, and DFT studies. [PDF]

PLoS One
Hawash M, Ghannam D, Dawoud L, Dawoud M, Eid A, Alhajj L, Qaoud MT.   +6 more
europepmc   +1 more source

A Wagner-Meerwein-like rearrangement shapes the structures of the fischerazoles, cyanobacterial polychlorinated lipopeptides

Leao P, Figueiredo S, Abt K, Viehrig K, Jervis P, Martins T, Lacomba I, Castagnolo D.   +7 more
europepmc   +1 more source

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Thiazole-Mediated Synthetic Methodology

Chemical Reviews, 2004
Review of synthetic schemes which have been developed in about 20 years of research by the use of thiazole-based methodology may serve to illustrate the potential of this approach in synthetic programs toward the construction of complex systems or special molecular fragments.
Alessandro Dondoni, Alberto Marra
exaly   +3 more sources

Thiazoles

ChemInform, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
D. Kikelj, U. Urleb
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Antiprotozoal thiazoles. 2-(5-Nitro-2-thienyl)thiazoles

Journal of Medicinal Chemistry, 1975
A series of 2-(5-nitro-2-thienyl)thiazoles and their vinylogs having substituted methylamine side chains has been prepared by halogen displacement on the corresponding 4-chloromethylthiazole. Of these, 4-morpholinomethyl-2-(5-nitro-2-thienyl)thiazole showed moderate activity against Trypanosoma cruzi and Trypanosoma rhodesiense in mice.
J P, Verge, P, Roffey
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Synthesis of Oligonucleotides Containing Thiazole and Thiazole N-Oxide Nucleobases

Organic Letters, 2002
[reaction: see text] The thiazole C-nucleoside analogue was synthesized by the Hantzsch cyclization method to form the thiazole ring and was then converted to the thiazole N-oxide C-nucleoside analogue by peracid oxidation of the heterocycle nitrogen.
Tod J, Miller, Hannah D, Farquar, Arsham, Sheybani, Camille E, Tallini, Andrea S, Saurage, Frank R, Fronczek, Robert P, Hammer   +6 more
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Thiazol‐Verbindungen, IV. Neue Rimifon‐Analoga mit Thiazol‐Ring

Justus Liebigs Annalen der Chemie, 1968
AbstractEs werden 2‐[Pyridyl‐(4)]‐thiazol‐carbonsäure‐(4)‐hydrazid (3) und mehrere Derivate mit potentiell tuberkulostatischer Aktivität hergestellt, z. B. das Carbonsäurehydrazid 10, die tricyclische Substanz 11 und das Oxim 12, das nach Neberscher Umlagerung 2‐[Pyridin‐(4)]‐4‐acetaminoacetylthiazol (17) liefert.
András Benkó, Albert Levente
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Pyrrolo[2,1‐b]thiazoles

ChemInform, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
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