BIOMAT Database Logo BIOMAT Database Logo

[Antiviral and antibacterial activities of 3-(substituted benzenesulfonylamino)-5,6-di(p-substituted phenyl)-1,2,4-triazines]. 1988

S Yoshii, and K Miyamoto, and T Nishimura

UI MeSH Term Description Entries
D000998 Antiviral Agents Agents used in the prophylaxis or therapy of VIRUS DISEASES. Some of the ways they may act include preventing viral replication by inhibiting viral DNA polymerase; binding to specific cell-surface receptors and inhibiting viral penetration or uncoating; inhibiting viral protein synthesis; or blocking late stages of virus assembly. Antiviral,Antiviral Agent,Antiviral Drug,Antivirals,Antiviral Drugs,Agent, Antiviral,Agents, Antiviral,Drug, Antiviral,Drugs, Antiviral
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
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
D013450 Sulfones Sulfone
D014227 Triazines Heterocyclic rings containing three nitrogen atoms, commonly in 1,2,4 or 1,3,5 or 2,4,6 formats. Some are used as HERBICIDES. Triazine,Benzotriazines

Related Publications

S Yoshii, and K Miyamoto, and T Nishimura
Synthesis, antituberculostatic, antifungal and antibacterial activities of 3-substituted phenyl-6-substituted phenyl-1,2,4-triazolo[4,3-b]pyridazines.
January 2010, Acta poloniae pharmaceutica,
S Yoshii, and K Miyamoto, and T Nishimura
One pot synthesis and SAR of some novel 3-substituted 5,6-diphenyl-1,2,4-triazines as antifungal agents.
January 2010, Bioorganic & medicinal chemistry letters,
S Yoshii, and K Miyamoto, and T Nishimura
Synthesis and anti-inflammatory evaluation of 3-methylthio-1,2,4-triazines, 3-alkoxy-1,2,4-triazines, and 3-aryloxy-1,2,4-triazines.
March 1980, Journal of pharmaceutical sciences,
S Yoshii, and K Miyamoto, and T Nishimura
New chromogens of the ferroin type-VIII Some di- and trisubstituted 1,2,4-triazines, 3-substituted-9H-indeno[1,2-e]-1,2,4-triazin-9-ones, and di- and trisubstituted 1,2,4-triazolines.
November 1977, Talanta,
S Yoshii, and K Miyamoto, and T Nishimura
[Antiviral compounds. XVI. Antiviral activity of 1,2,4-triazines].
April 1987, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
S Yoshii, and K Miyamoto, and T Nishimura
A regioselective approach to 5-substituted-3-amino-1,2,4-triazines.
June 2003, Organic letters,
S Yoshii, and K Miyamoto, and T Nishimura
Studies on anti-platelet agents. V. Synthesis and structure-activity relationship of 3-substituted 5,6-bis(4-methoxyphenyl)-1,2,4-triazines.
September 1994, Chemical & pharmaceutical bulletin,
S Yoshii, and K Miyamoto, and T Nishimura
Synthesis and antihypertensive activity of novel 3-hydrazino-5-phenyl-1,2,4-triazines.
June 1979, Journal of medicinal chemistry,
S Yoshii, and K Miyamoto, and T Nishimura
Preparation of a Series of 5-Methyl-3-(substituted)-[1,2,4]triazines.
June 2011, Tetrahedron letters,
S Yoshii, and K Miyamoto, and T Nishimura
Antimalarials. 3. 1,2,4-Triazines.
June 1976, Journal of medicinal chemistry,
Copied contents to your clipboard!