BIOMAT Database Logo BIOMAT Database Logo

Syntheses of 23-C-substituted derivatives of mycaminosyl tylonolide. 1986

T Tsuchiya, and S Sakamoto, and N Kajikawa, and S Umezawa, and M Hamada, and H Umezawa

UI MeSH Term Description Entries
D007933 Leucomycins An antibiotic complex produced by Streptomyces kitasatoensis. The complex consists of a mixture of at least eight biologically active components, A1 and A3 to A9. Leucomycins have both antibacterial and antimycoplasmal activities.
D009682 Magnetic Resonance Spectroscopy Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING). In Vivo NMR Spectroscopy,MR Spectroscopy,Magnetic Resonance,NMR Spectroscopy,NMR Spectroscopy, In Vivo,Nuclear Magnetic Resonance,Spectroscopy, Magnetic Resonance,Spectroscopy, NMR,Spectroscopy, Nuclear Magnetic Resonance,Magnetic Resonance Spectroscopies,Magnetic Resonance, Nuclear,NMR Spectroscopies,Resonance Spectroscopy, Magnetic,Resonance, Magnetic,Resonance, Nuclear Magnetic,Spectroscopies, NMR,Spectroscopy, MR
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D051379 Mice The common name for the genus Mus. Mice, House,Mus,Mus musculus,Mice, Laboratory,Mouse,Mouse, House,Mouse, Laboratory,Mouse, Swiss,Mus domesticus,Mus musculus domesticus,Swiss Mice,House Mice,House Mouse,Laboratory Mice,Laboratory Mouse,Mice, Swiss,Swiss Mouse,domesticus, Mus musculus

Related Publications

T Tsuchiya, and S Sakamoto, and N Kajikawa, and S Umezawa, and M Hamada, and H Umezawa
Syntheses of derivatives of 4'-deoxymycaminosyl tylonolide and mycaminosyl tylonolide modified AT C-23.
October 1981, The Journal of antibiotics,
T Tsuchiya, and S Sakamoto, and N Kajikawa, and S Umezawa, and M Hamada, and H Umezawa
Syntheses of 23-dialkylamino derivatives of mycaminosyl tylonolide and 4'-deoxymycaminosyl tylonolide effective against gram-negative bacteria.
January 1982, The Journal of antibiotics,
T Tsuchiya, and S Sakamoto, and N Kajikawa, and S Umezawa, and M Hamada, and H Umezawa
Syntheses of 23-C-alkylidene, and 23-N-containing derivatives of 5-O-mycaminosyltylonolide.
April 1987, The Journal of antibiotics,
T Tsuchiya, and S Sakamoto, and N Kajikawa, and S Umezawa, and M Hamada, and H Umezawa
Syntheses of potentially active 1-substituted imidazo-[1,2-c]pyrimidine derivatives.
February 1986, Archiv der Pharmazie,
T Tsuchiya, and S Sakamoto, and N Kajikawa, and S Umezawa, and M Hamada, and H Umezawa
Syntheses of substituted 8-aminopurine derivatives.
July 1974, Chemical & pharmaceutical bulletin,
T Tsuchiya, and S Sakamoto, and N Kajikawa, and S Umezawa, and M Hamada, and H Umezawa
Formation of an antibacterial metabolite from a new macrolide compound 23-O-benzyl-5-mycaminosyl-tylonolide (TMC-101), by a hepatic microsomal drug-metabolizing enzyme system.
July 1991, Journal of pharmacobio-dynamics,
T Tsuchiya, and S Sakamoto, and N Kajikawa, and S Umezawa, and M Hamada, and H Umezawa
Short syntheses of 1-substituted dibenzothiophene derivatives.
March 2021, Organic & biomolecular chemistry,
T Tsuchiya, and S Sakamoto, and N Kajikawa, and S Umezawa, and M Hamada, and H Umezawa
Syntheses of 9-substituted josamycin, 13-substituted isojosamycin and their tetrahydro derivatives.
September 1981, The Journal of antibiotics,
T Tsuchiya, and S Sakamoto, and N Kajikawa, and S Umezawa, and M Hamada, and H Umezawa
Studies on the syntheses of 1-substituted benzimidazole derivatives.
January 2004, Acta poloniae pharmaceutica,
T Tsuchiya, and S Sakamoto, and N Kajikawa, and S Umezawa, and M Hamada, and H Umezawa
Syntheses of 3-substituted pyrrole derivatives with antiinflammatory activity.
August 1980, Chemical & pharmaceutical bulletin,
Copied contents to your clipboard!