BIOMAT Database Logo BIOMAT Database Logo

[Synthesis of quaternary ammonium compounds and a study of their antimicrobial activity]. 1978

M Kh Gluzman, and G Ia Kivman, and E I Pogorelyĭ, and M N Bel'skaia, and V P Rubtsova

UI MeSH Term Description Entries
D008826 Microbial Sensitivity Tests Any tests that demonstrate the relative efficacy of different chemotherapeutic agents against specific microorganisms (i.e., bacteria, fungi, viruses). Bacterial Sensitivity Tests,Drug Sensitivity Assay, Microbial,Minimum Inhibitory Concentration,Antibacterial Susceptibility Breakpoint Determination,Antibiogram,Antimicrobial Susceptibility Breakpoint Determination,Bacterial Sensitivity Test,Breakpoint Determination, Antibacterial Susceptibility,Breakpoint Determination, Antimicrobial Susceptibility,Fungal Drug Sensitivity Tests,Fungus Drug Sensitivity Tests,Sensitivity Test, Bacterial,Sensitivity Tests, Bacterial,Test, Bacterial Sensitivity,Tests, Bacterial Sensitivity,Viral Drug Sensitivity Tests,Virus Drug Sensitivity Tests,Antibiograms,Concentration, Minimum Inhibitory,Concentrations, Minimum Inhibitory,Inhibitory Concentration, Minimum,Inhibitory Concentrations, Minimum,Microbial Sensitivity Test,Minimum Inhibitory Concentrations,Sensitivity Test, Microbial,Sensitivity Tests, Microbial,Test, Microbial Sensitivity,Tests, Microbial Sensitivity
D011725 Pyridines Compounds with a six membered aromatic ring containing NITROGEN. The saturated version is PIPERIDINES.
D000644 Quaternary Ammonium Compounds Derivatives of ammonium compounds, NH4+ Y-, in which all four of the hydrogens bonded to nitrogen have been replaced with hydrocarbyl groups. These are distinguished from IMINES which are RN Quaternary Ammonium Compound,Ammonium Compound, Quaternary,Ammonium Compounds, Quaternary,Compound, Quaternary Ammonium
D000890 Anti-Infective Agents Substances that prevent infectious agents or organisms from spreading or kill infectious agents in order to prevent the spread of infection. Anti-Infective Agent,Anti-Microbial Agent,Antimicrobial Agent,Microbicide,Microbicides,Anti-Microbial Agents,Antiinfective Agents,Antimicrobial Agents,Agent, Anti-Infective,Agent, Anti-Microbial,Agent, Antimicrobial,Agents, Anti-Infective,Agents, Anti-Microbial,Agents, Antiinfective,Agents, Antimicrobial,Anti Infective Agent,Anti Infective Agents,Anti Microbial Agent,Anti Microbial Agents
D001548 Benzalkonium Compounds A mixture of alkylbenzyldimethylammonium compounds. It is a bactericidal quaternary ammonium detergent used topically in medicaments, deodorants, mouthwashes, as a surgical antiseptic, and as a as preservative and emulsifier in drugs and cosmetics. Benzalkonium,Benzalkonium Chloride,Alkyldimethylbenzylammonium Chloride,Asepsol,BTC-2125,Drapolene,Germex,Osvan,Zephiran,BTC 2125,BTC2125,Chloride, Alkyldimethylbenzylammonium,Chloride, Benzalkonium,Compounds, Benzalkonium
D013329 Structure-Activity Relationship The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups. Relationship, Structure-Activity,Relationships, Structure-Activity,Structure Activity Relationship,Structure-Activity Relationships

Related Publications

M Kh Gluzman, and G Ia Kivman, and E I Pogorelyĭ, and M N Bel'skaia, and V P Rubtsova
[Antimicrobial activity of quaternary ammonium compounds].
June 1990, Die Pharmazie,
M Kh Gluzman, and G Ia Kivman, and E I Pogorelyĭ, and M N Bel'skaia, and V P Rubtsova
Synthesis and antimicrobial activity of new quaternary ammonium chlorides.
June 1996, Archiv der Pharmazie,
M Kh Gluzman, and G Ia Kivman, and E I Pogorelyĭ, and M N Bel'skaia, and V P Rubtsova
Soft antimicrobial agents: synthesis and activity of labile environmentally friendly long chain quaternary ammonium compounds.
September 2003, Journal of medicinal chemistry,
M Kh Gluzman, and G Ia Kivman, and E I Pogorelyĭ, and M N Bel'skaia, and V P Rubtsova
Synthesis and antimicrobial activity of quaternary ammonium silane coupling agents.
January 2011, Journal of oleo science,
M Kh Gluzman, and G Ia Kivman, and E I Pogorelyĭ, and M N Bel'skaia, and V P Rubtsova
Natural product-derived quaternary ammonium compounds with potent antimicrobial activity.
April 2016, The Journal of antibiotics,
M Kh Gluzman, and G Ia Kivman, and E I Pogorelyĭ, and M N Bel'skaia, and V P Rubtsova
Polymeric Quaternary Ammonium Compounds: Versatile Antimicrobial Materials.
January 2017, Current topics in medicinal chemistry,
M Kh Gluzman, and G Ia Kivman, and E I Pogorelyĭ, and M N Bel'skaia, and V P Rubtsova
Synthesis, physiochemical property and antimicrobial activity of novel quaternary ammonium salts.
December 2018, Journal of enzyme inhibition and medicinal chemistry,
M Kh Gluzman, and G Ia Kivman, and E I Pogorelyĭ, and M N Bel'skaia, and V P Rubtsova
QUATERNARY AMMONIUM COMPOUNDS. IV. ANTIACETYLCHOLINESTERASE ACTIVITY AND RING SIZE IN AROMATIC QUATERNARY AMMONIUM COMPOUNDS.
July 1963, Journal of medicinal chemistry,
M Kh Gluzman, and G Ia Kivman, and E I Pogorelyĭ, and M N Bel'skaia, and V P Rubtsova
QUATERNARY AMMONIUM COMPOUNDS. 3. ANTIACETYLCHOLINESTERASE ACTIVITY AND CHARGE DISTRIBUTION IN AROMATIC QUATERNARY AMMONIUM COMPOUNDS.
March 1963, Journal of medicinal chemistry,
M Kh Gluzman, and G Ia Kivman, and E I Pogorelyĭ, and M N Bel'skaia, and V P Rubtsova
Corrigendum: Natural product-derived quaternary ammonium compounds with potent antimicrobial activity.
October 2016, The Journal of antibiotics,
Copied contents to your clipboard!