BIOMAT Database Logo BIOMAT Database Logo

[Synthesis and antibacterial activity in vitro of the potassium salts of aroyl-hydrazino-carbodithioic acids and of some 2-mercapto-5-aryl-1,3,4-oxadiazoles]. 1977

G Mazzone, and F Bonina, and S Cosentino, and G Iacona

UI MeSH Term Description Entries
D010069 Oxadiazoles Compounds containing five-membered heteroaromatic rings containing two carbons, two nitrogens, and one oxygen atom which exist in various regioisomeric forms. Oxadiazole
D006834 Hydrazines Substituted derivatives of hydrazine (formula H2N-NH2). Hydrazide
D001419 Bacteria One of the three domains of life (the others being Eukarya and ARCHAEA), also called Eubacteria. They are unicellular prokaryotic microorganisms which generally possess rigid cell walls, multiply by cell division, and exhibit three principal forms: round or coccal, rodlike or bacillary, and spiral or spirochetal. Bacteria can be classified by their response to OXYGEN: aerobic, anaerobic, or facultatively anaerobic; by the mode by which they obtain their energy: chemotrophy (via chemical reaction) or PHOTOTROPHY (via light reaction); for chemotrophs by their source of chemical energy: CHEMOLITHOTROPHY (from inorganic compounds) or chemoorganotrophy (from organic compounds); and by their source for CARBON; NITROGEN; etc.; HETEROTROPHY (from organic sources) or AUTOTROPHY (from CARBON DIOXIDE). They can also be classified by whether or not they stain (based on the structure of their CELL WALLS) with CRYSTAL VIOLET dye: gram-negative or gram-positive. Eubacteria
D013438 Sulfhydryl Compounds Compounds containing the -SH radical. Mercaptan,Mercapto Compounds,Sulfhydryl Compound,Thiol,Thiols,Mercaptans,Compound, Sulfhydryl,Compounds, Mercapto,Compounds, Sulfhydryl
D013859 Thiocarbamates Carbamates in which the -CO- group has been replaced by a -CS- group. Thiocarbamate

Related Publications

G Mazzone, and F Bonina, and S Cosentino, and G Iacona
[Synthesis and antibacterial activity of 2-(3-pyridyl)-5-([(5-aryl-1,3,4-oxadiazol-2-yl) methylene]thio)-1,3,4-oxadiazoles].
April 2004, Yao xue xue bao = Acta pharmaceutica Sinica,
G Mazzone, and F Bonina, and S Cosentino, and G Iacona
Synthesis and Pharmacological Activities of Some New 5-Substituted-2-mercapto-1,3,4-oxadiazoles.
September 2011, Indian journal of pharmaceutical sciences,
G Mazzone, and F Bonina, and S Cosentino, and G Iacona
Antihypertensive thiadiazoles. 1. Synthesis of some 2-aryl-5-hydrazino-1,3,4-thiadiazoles with vasodilator activity.
May 1988, Journal of medicinal chemistry,
G Mazzone, and F Bonina, and S Cosentino, and G Iacona
Synthesis of 2-aryl-5-(arylsulfonyl)-1,3,4-oxadiazoles as potent antibacterial and antioxidant agents.
January 2022, Turkish journal of chemistry,
G Mazzone, and F Bonina, and S Cosentino, and G Iacona
Synthesis and antimicrobial activity of some 5-aryl-2-[N,N-disubstituted thiocarbamoylthio)acylamino]-1,3,4-oxadiazoles.
January 1998, Farmaco (Societa chimica italiana : 1989),
G Mazzone, and F Bonina, and S Cosentino, and G Iacona
Synthesis and evaluation of in vitro antimicrobial activity of novel 2-[2-(aroyl)aroyloxy]methyl-1,3,4-oxadiazoles.
January 2014, Bioorganicheskaia khimiia,
G Mazzone, and F Bonina, and S Cosentino, and G Iacona
Synthesis and in vitro antibacterial activity of some N-(5-aryl-1,3,4-thiadiazole-2-yl)piperazinyl quinolone derivatives.
October 2003, Farmaco (Societa chimica italiana : 1989),
G Mazzone, and F Bonina, and S Cosentino, and G Iacona
Synthesis of some new heterocyclic 1,3,4-oxadiazoles with antibacterial activity.
June 1982, Die Pharmazie,
G Mazzone, and F Bonina, and S Cosentino, and G Iacona
[Synthesis of some 5-aryl-2-dimethylamino-1,3,4-oxadiazoles endowed with anti-inflammatory properties].
January 1966, Bulletin de la Societe chimique de France,
G Mazzone, and F Bonina, and S Cosentino, and G Iacona
Synthesis and antibacterial activity of 5-aryl-2-[(alpha-chloro-alpha-phenylacetyl/alpha-bromopropionyl)amino]- 1,3,4-oxadiazoles and 2-[(5-aryl-1,3,4-oxadiazol-2-yl)imino]-5-phenyl/methyl-4-thiazolidinone s.
October 1997, Arzneimittel-Forschung,
Copied contents to your clipboard!