Studies on new catechol containing cephalosporins. I. Synthesis and structure-activity relationships of cephalosporins having a catechol moiety at the C-3 position. 1995

K I Choi, and J H Cha, and A N Pae, and Y S Cho, and H Y Kang, and H Y Koh, and M H Chang
Division of Applied Science, Korea Institute of Science and Technology, Seoul, Korea.

UI MeSH Term Description Entries
D002396 Catechols A group of 1,2-benzenediols that contain the general formula R-C6H5O2. Pyrocatechols,o-Dihydroxybenzenes,ortho-Dihydroxybenzenes,o Dihydroxybenzenes,ortho Dihydroxybenzenes
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
D006090 Gram-Negative Bacteria Bacteria which lose crystal violet stain but are stained pink when treated by Gram's method. Gram Negative Bacteria
D006094 Gram-Positive Bacteria Bacteria which retain the crystal violet stain when treated by Gram's method. Gram Positive Bacteria
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
D015394 Molecular Structure The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds. Structure, Molecular,Molecular Structures,Structures, Molecular

Related Publications

K I Choi, and J H Cha, and A N Pae, and Y S Cho, and H Y Kang, and H Y Koh, and M H Chang
November 1996, The Journal of antibiotics,
K I Choi, and J H Cha, and A N Pae, and Y S Cho, and H Y Kang, and H Y Koh, and M H Chang
July 1992, Journal of medicinal chemistry,
K I Choi, and J H Cha, and A N Pae, and Y S Cho, and H Y Kang, and H Y Koh, and M H Chang
December 1994, The Journal of antibiotics,
K I Choi, and J H Cha, and A N Pae, and Y S Cho, and H Y Kang, and H Y Koh, and M H Chang
November 2016, European journal of medicinal chemistry,
K I Choi, and J H Cha, and A N Pae, and Y S Cho, and H Y Kang, and H Y Koh, and M H Chang
May 1991, The Journal of antibiotics,
K I Choi, and J H Cha, and A N Pae, and Y S Cho, and H Y Kang, and H Y Koh, and M H Chang
November 1981, The Journal of antibiotics,
K I Choi, and J H Cha, and A N Pae, and Y S Cho, and H Y Kang, and H Y Koh, and M H Chang
May 2000, Bioorganic & medicinal chemistry,
K I Choi, and J H Cha, and A N Pae, and Y S Cho, and H Y Kang, and H Y Koh, and M H Chang
December 1991, Chemical & pharmaceutical bulletin,
K I Choi, and J H Cha, and A N Pae, and Y S Cho, and H Y Kang, and H Y Koh, and M H Chang
March 1986, The Journal of antibiotics,
K I Choi, and J H Cha, and A N Pae, and Y S Cho, and H Y Kang, and H Y Koh, and M H Chang
April 2001, Archives of pharmacal research,
Copied contents to your clipboard!