Results 71 to 80 of about 1,311 (155)
Background Pyrazolo[1,5-a]pyrimidines are purine analogues. They have beneficial properties as antimetabolites in purine biochemical reactions. This division compounds have attracted wide pharmaceutical interest because of their antitrypanosomal activity.
Nadia A. Abdelriheem +2 more
doaj +1 more source
3-(2-Fluorophenyl)-6-(phenoxymethyl)-1,2,4-triazolo[3,4-b][1,3,4]thiadiazole
The crystal structure of the title compound, C16H11FN4OS, was synthesized in the course of our studies on 1,2,4-triazolo[3,4-b][1,3,4]thiadiazoles as inhibitors of p38 mitogen-activated protein kinase (MAPK). The three-dimensional data obtained were used
Stefan Laufer +2 more
doaj +1 more source
2-Amino-5-propyl-1,3,4-thiadiazole
The title compound, C5H9N3S, which exhibits a hypoglycemic effect, crystallizes in space group P21/c. The structure is held together by a network of intermolecular N—H⋯N hydrogen bonds.
Choudhury, Angshuman Roy +4 more
openaire +2 more sources
Synthesis and Anticancer Activity of 1,3,4-Thiadiazoles with 3-Methoxyphenyl Substituent. [PDF]
Janowska S +7 more
europepmc +1 more source
5,5′-Dimethyl-2,2′-dithiodi-1,3,4-thiadiazole
The title compound, C6H6N4S4, is formed through the thionato S—S bonding of parent 2-mercapto-5-methyl-1,3,4-thiadiazole molecules, following the deprotonation of thiol groups in a mixed solvent. The title compound crystallizes in the monoclinic system, space group C2/c. The S—S distance is 2.028 (1) A, typical of a single bond.
Jun-Ling Song +3 more
openaire +1 more source
Background Expression and activity of heparanase, an endoglycosidase that cleaves heparan sulfate (HS) side chains of proteoglycans, is associated with progression and poor prognosis of many cancers which makes it an attractive drug target in cancer ...
C. P. Baburajeev +9 more
doaj +1 more source
Identification of 2-Aminoacyl-1,3,4-thiadiazoles as Prostaglandin E2 and Leukotriene Biosynthesis Inhibitors. [PDF]
Potenza M +15 more
europepmc +1 more source
Design, Synthesis, Antibacterial Evaluations and In Silico Studies of Novel Thiosemicarbazides and 1,3,4-Thiadiazoles. [PDF]
Janowska S +3 more
europepmc +1 more source
New 1,3,4-thiadiazoles as potential anticancer agents: pro-apoptotic, cell cycle arrest, molecular modelling, and ADMET profile. [PDF]
Hekal MH +5 more
europepmc +1 more source
Exploring the Antiparasitic Activity of Tris-1,3,4-Thiadiazoles against Toxoplasma gondii-Infected Mice. [PDF]
Almutairi TM +8 more
europepmc +1 more source

