BIOMAT Database Logo BIOMAT Database Logo

[Biological properties of some new antibacterial antibiotics. I. Activities of some derivatives of 6-aminopenicillanic acid (6-AP) and 7-aminocephallosporanic acid (7-AC)]. 1975

D Jastalska, and M Zapaśnik, and J Gralewicz, and W Morris-Rostkowska, and W Chojnowski

UI MeSH Term Description Entries
D010397 Penicillanic Acid A building block of penicillin, devoid of significant antibacterial activity. (From Merck Index, 11th ed) Acid, Penicillanic
D002511 Cephalosporins A group of broad-spectrum antibiotics first isolated from the Mediterranean fungus ACREMONIUM. They contain the beta-lactam moiety thia-azabicyclo-octenecarboxylic acid also called 7-aminocephalosporanic acid. Antibiotics, Cephalosporin,Cephalosporanic Acid,Cephalosporin,Cephalosporin Antibiotic,Cephalosporanic Acids,Acid, Cephalosporanic,Acids, Cephalosporanic,Antibiotic, Cephalosporin,Cephalosporin Antibiotics
D004352 Drug Resistance, Microbial The ability of microorganisms, especially bacteria, to resist or to become tolerant to chemotherapeutic agents, antimicrobial agents, or antibiotics. This resistance may be acquired through gene mutation or foreign DNA in transmissible plasmids (R FACTORS). Antibiotic Resistance,Antibiotic Resistance, Microbial,Antimicrobial Resistance, Drug,Antimicrobial Drug Resistance,Antimicrobial Drug Resistances,Antimicrobial Resistances, Drug,Drug Antimicrobial Resistance,Drug Antimicrobial Resistances,Drug Resistances, Microbial,Resistance, Antibiotic,Resistance, Drug Antimicrobial,Resistances, Drug Antimicrobial
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

Related Publications

D Jastalska, and M Zapaśnik, and J Gralewicz, and W Morris-Rostkowska, and W Chojnowski
Synthesis and some biological properties of 6-aminopenicillanic derivatives.
January 1977, Polish journal of pharmacology and pharmacy,
D Jastalska, and M Zapaśnik, and J Gralewicz, and W Morris-Rostkowska, and W Chojnowski
Synthesis of 6-aminopenicillanic acid derivatives. I. 6-(Acylureido) penicillanates and some related compounds.
July 1965, The Journal of antibiotics,
D Jastalska, and M Zapaśnik, and J Gralewicz, and W Morris-Rostkowska, and W Chojnowski
Derivatives of 6-aminopenicillanic acid. VI. Synthesis of some derivatives of 6-aminothiopenicillanic acid.
November 1965, Journal of medicinal chemistry,
D Jastalska, and M Zapaśnik, and J Gralewicz, and W Morris-Rostkowska, and W Chojnowski
6-Aminopenicillanic acid. I. 6-Aminopenicillanic acid in penicillin fermentations.
August 1961, Proceedings of the Royal Society of London. Series B, Biological sciences,
D Jastalska, and M Zapaśnik, and J Gralewicz, and W Morris-Rostkowska, and W Chojnowski
Synthesis and antibacterial activity of new arylamido derivatives of 6 beta-aminopenicillanic, 7 beta-aminocephalosporanic and 7 beta-aminodesacetoxycephalosporanic acids.
July 2000, Arzneimittel-Forschung,
D Jastalska, and M Zapaśnik, and J Gralewicz, and W Morris-Rostkowska, and W Chojnowski
[Derivatives of 6-aminopenicillanic acid. I. Synthesis of 6-(substituted acrylamido) penicillanic acid].
August 1965, Yao xue xue bao = Acta pharmaceutica Sinica,
D Jastalska, and M Zapaśnik, and J Gralewicz, and W Morris-Rostkowska, and W Chojnowski
Design, synthesis and biological activities of some 7-aminocephalosporanic acid derivatives.
November 2013, European journal of medicinal chemistry,
D Jastalska, and M Zapaśnik, and J Gralewicz, and W Morris-Rostkowska, and W Chojnowski
Synthesis of 6-aminopenicillanic acid derivatives.
May 1966, Chemistry & industry,
D Jastalska, and M Zapaśnik, and J Gralewicz, and W Morris-Rostkowska, and W Chojnowski
Modification of 6-aminopenicillanic acid derivatives.
January 1976, Polish journal of pharmacology and pharmacy,
D Jastalska, and M Zapaśnik, and J Gralewicz, and W Morris-Rostkowska, and W Chojnowski
Behaviour of some derivatives of 7-aminocephalosporanic acid and 6-aminopenicillanic acidas substrates, inhibitors and inducers of penicillinases.
April 1962, The Biochemical journal,
Copied contents to your clipboard!