Results 161 to 170 of about 4,281 (225)

Synthesis, Anticancer Evaluation, and Molecular Docking of Novel Thiazolobenzimidazole-Thiazole Hybrids as Potent Colon Cancer Inhibitors. [PDF]

ChemistryOpen
Huwaimel B, Abouzied AS, Zaki MEA, Alamri A, Farag B, Alqarni S, Gomha SM.   +6 more
europepmc   +1 more source

Targeting Glutaminase Isoforms GLS and GLS2 in Luminal Breast Cancer. [PDF]

Int J Mol Sci
Masisi BK, El Ansari R, Fakroun A, Erkan B, Rakha EA, Green AR.   +5 more
europepmc   +1 more source

Machine learning prediction of multiple distinct high-affinity chemotypes for α-synuclein fibrils. [PDF]

Chem Commun (Camb)
Li X, Perez RM, Tu Z, Mach RH, Giannakoulias S, Petersson EJ.   +5 more
europepmc   +1 more source

Promising Norlabdane-Heterocyclic Hybrids: Synthesis, Structural Characterization and Antimicrobial Activity Evaluation. [PDF]

Pharmaceuticals (Basel)
Lungu L, Ciocarlan A, Mangalagiu II, Aricu A.   +3 more
europepmc   +1 more source

Synthesis and Bioactivity Studies of Benzimidazole-Chalcone Hybrids. [PDF]

Molecules
Makgoathana HD, Mthembu ST, Mhlanga TV, Selepe MA, Sonopo MS.   +4 more
europepmc   +1 more source

Recent advances in non-conventional synthesis of N-heterocyclic compounds: emerging strategies and biological perspectives. [PDF]

RSC Adv
Sivaraj N, Sakthivel K, Kikushima K, Kostić MD, Dohi T, Singh FV.   +5 more
europepmc   +1 more source

Thiazolyl-Methylthio-1,3,4-Thiadiazole Hybrids as Halicin Analogues with Antimicrobial and Antibiofilm Activities: Chemical Development, Biological Assessment, and 2D-QSAR Study. [PDF]

Antibiotics (Basel)
Ungureanu D, Marc G, Duma MN, Vodnar DC, Martău GA, Vlase L, Pîrnău A, Tiperciuc B, Moldovan C, Ionuț I, Stana A, Oniga I, Oniga O.   +12 more
europepmc   +1 more source

Azodicarboxylates: valuable reagents for the multicomponent synthesis of novel 1,3,4-thiadiazoles and imidazo[2,1-b][1,3,4]thiadiazoles

Tetrahedron, 2013
Summarization: Upon reaction of 4,5-disubstituted-N-arylaminoimidazole-2-thiones with isocyanides in the presence of azodicarboxylates (1.2 equiv) at rt, the imidazo[2,1-b][1,3,4]thiadiazoles were formed as the only reaction products in very good yields,
Tryfon Zarganes-Tzitzikas, Constantinos G Neochoritis, Julia Stephanidou-Stephanatou   +2 more
exaly   +2 more sources

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Thiadiazoles

2011
Ugo Chiacchio
exaly   +4 more sources

A 1,2,3-thiadiazole–1,2,3-thiadiazole rearrangement

J. Chem. Soc., Chem. Commun., 1983
During its preparation, 4-ethoxycarbonyl-5-diazomethyl-1,2,3-thiadiazole (4), undergoes a ring transformation into the isomeric structure (5), but when the ester function in (4) is replaced by a phenyl group, no isomerization is observed.
Gerrit L'abbé, Jean-Paul Dekerk, Martine Deketele   +2 more
openaire   +1 more source