Results 91 to 100 of about 8,138 (214)

Room Temperature Synthesis and Antibacterial Activity of New Sulfonamides Containing N,N -Diethyl-Substituted AmidoMoieties [PDF]

open access: yes, 2012
Sulfonamide drugs which have brought about an antibiotic revolution in medicine are associated with a wide range of biological activities.
Ajani, Olayinka O.   +4 more
core   +5 more sources

2-Amino-1,3,4-thiadiazole as a potential scaffold for promising antimicrobial agents

open access: yesDrug Design, Development and Therapy, 2018
Georgeta Serban,1,* Oana Stanasel,2,* Eugenia Serban,3 Sanda Bota2,* 1Pharmaceutical Chemistry Department, Faculty of Medicine and Pharmacy, University of Oradea, Oradea, Romania; 2Chemistry Department, Faculty of Sciences, University of Oradea, Oradea,
Serban G, Stanasel O, Serban E, Bota S
doaj  

Synthesis, Characterization and Antibacterial Activity of New Chalcones Derived from New Aldehyde; 4-[5-(4`tolyl)-1,3,4-thiadiazole-2-yl] benzaldehyde

open access: yesIbn Al-Haitham Journal for Pure and Applied Sciences, 2017
 New chalcones of  -{ -  -   -   y  -     - hi di z  e- -y    he y  - -    e e- -  e-    -        - substituted phenyl have been prepared from condensation of  a new of  4-[5-(4`-tolyl)1,3,4-thiadiazole-2-yl] benzaldehyde (which is synthesized by the ...
Jumbad H. Tomma.   +2 more
doaj   +1 more source

Synthesis, Characterisation and Biological Activities of Nitrogen-Sulphur Ligands and Their Transition Metal Complexes [PDF]

open access: yes, 2008
Synthetic compounds, especially those containing heterocyclic ring systems composed of nitrogen and sulphur have been of great interest due to their versatility as medicinal drugs.
Begum, Thahira
core  

A survey of liquid crystalline oxadiazoles

open access: yes, 2008
We propose a survey of those oxadiazole compounds, which are mesogenic. We will see that they can have bend-shaped molecules, a biaxial nematic phase, or other interesting peculiarities in the nematic and smectic phase.
Sparavigna, Amelia
core   +1 more source

2,2′-[(1,3,4-Thiadiazole-2,5-diyl)bis(sulfanediyl)]diacetonitrile

open access: yesActa Crystallographica Section E, 2013
In the title compound, C6H4N4S3, the 1,3,4-thiadiazole ring is essentially planar, with an r.m.s. deviation of 0.001 Å. The two N—C—S—C torsion angles in the molecule are −23.41 (15) and 0.62 (14)°. One
Mustafa R. Albayati   +4 more
doaj   +1 more source

Synthesis, diuretic activity research and QSAR-analysis of N-(1,3,4-tiadiazol-2-il)substituted amides of alkanecarboxylic acids

open access: yesФармацевтичний журнал, 2019
Diuretics are effective drugs that are widely used in medicine, but have unwanted side effects. The derivative of thiadiazole – acetozolamide is a known diuretic.
І. V. Drapak
doaj   +1 more source

Synthesis of Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole and Its Analgesic, Anti-Inflammatory and Anti-Bacterial Activity

open access: yesE-Journal of Chemistry, 2012
Schiff Bases of 2-amino-5-aryl-1,3,4-thiadiazole derivatives have been synthesized with different aromatic aldehyde. 1,3,4-thiadiazole derivatives were prepared by the reaction of thiosemicarbazide, sodium acetate and aromatic aldehyde. The structures of
Alok Pandey   +3 more
doaj   +1 more source

Mono- és bisz(acil)hidrazonok átalakulásai: Gyűrűs N,O,S-acetálok/ketálok szintézise. = Transformations of mono- and bis(acyl)hydrazones: Synthesis of cyclic N,O,S-acetals/ketals. [PDF]

open access: yes, 2007
Aldehid- és keton-tioszemikarbazonokat állítottunk elő, melyeket acilezési körülmények között 3-acil-1,3,4-tiadiazolinokká ciklizáltunk. A 2-monoszubsztituált heterogyűrűs vegyületek oxidáló, illetve dehidrogénező szerek [kálium permanganát és a most ...
Somogyi, László
core  

Crystal structure of 5-(adamantan-1-yl)-3-= (4-chloroanilino)methyl-2,3-dihydro-1,3,4-oxadiazole-2-thione, C19H22ClN3OS [PDF]

open access: yes, 2016
C19H22ClN3OS, orthorhombic, P212121 (no. 19), a = 7.0418(2) Å, b = 10.8802(3) Å, c = 23.5506(6) Å, V = 1804.36(8) Å3, Z = 4, R gt (F) = 0.0413, wR ref (F 2
Al-Alshaikh, M. A.   +5 more
core   +1 more source

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