BIOMAT Database Logo BIOMAT Database Logo

Synthesis and pharmacological evaluation of 1,4-dihydro-2H-3,1-benzoxazin-2-one derivatives. 1971

F De Marchi, and G F Tamagnone, and M V Torielli

UI MeSH Term Description Entries
D007928 Lethal Dose 50 The dose amount of poisonous or toxic substance or dose of ionizing radiation required to kill 50% of the tested population. LD50,Dose 50, Lethal
D008297 Male Males
D010078 Oxazines Six-membered heterocycles containing an oxygen and a nitrogen.
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
D000927 Anticonvulsants Drugs used to prevent SEIZURES or reduce their severity. Anticonvulsant,Anticonvulsant Drug,Anticonvulsive Agent,Anticonvulsive Drug,Antiepileptic,Antiepileptic Agent,Antiepileptic Agents,Antiepileptic Drug,Anticonvulsant Drugs,Anticonvulsive Agents,Anticonvulsive Drugs,Antiepileptic Drugs,Antiepileptics,Agent, Anticonvulsive,Agent, Antiepileptic,Agents, Anticonvulsive,Agents, Antiepileptic,Drug, Anticonvulsant,Drug, Anticonvulsive,Drug, Antiepileptic,Drugs, Anticonvulsant,Drugs, Anticonvulsive,Drugs, Antiepileptic
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
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

F De Marchi, and G F Tamagnone, and M V Torielli
Catalytic Asymmetric Chlorocyclization of 2-Vinylphenylcarbamates for Synthesis of 1,4-Dihydro-2H-3,1-benzoxazin-2-one Derivatives.
March 2017, Organic letters,
F De Marchi, and G F Tamagnone, and M V Torielli
Central pharmacological activities of 4-phenyl-6-chloro-1,4-dihydro-2H-3,1-benzoxazin-2-one.
February 1973, Archives internationales de pharmacodynamie et de therapie,
F De Marchi, and G F Tamagnone, and M V Torielli
Synthesis and antifungal activity of 2H-1,4-benzoxazin-3(4H)-one derivatives.
January 2016, Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes,
F De Marchi, and G F Tamagnone, and M V Torielli
2H-1,4-benzoxazin-2-ones.
July 1966, Journal of medicinal chemistry,
F De Marchi, and G F Tamagnone, and M V Torielli
THIO DERIVATIVES OF 2,3-DIHYDRO-4H-1,3-BENZOXAZIN-4-ONE. SYNTHESIS AND PHARMACOLOGICAL PROPERTIES.
May 1963, Journal of medicinal chemistry,
F De Marchi, and G F Tamagnone, and M V Torielli
Synthesis and biological evaluation of new 2-(4,5-dihydro-1H-imidazol-2-yl)-3,4-dihydro-2H-1,4-benzoxazine derivatives.
May 2003, Journal of medicinal chemistry,
F De Marchi, and G F Tamagnone, and M V Torielli
1,2-Dihydro-3,1-benzoxazin-4-one and 4H-1,2-dihydro-pyrido-[2,3-d]- [1,3]-oxazin-4-one derivatives as potential prodrugs. Part I: Synthesis.
October 1991, Archiv der Pharmazie,
F De Marchi, and G F Tamagnone, and M V Torielli
2-Phenyl-4H-3,1-benzoxazin-4-one.
December 2008, Acta crystallographica. Section E, Structure reports online,
F De Marchi, and G F Tamagnone, and M V Torielli
Synthesis of amidrazones from 2-ethoxycarbonyl-4H-3,1-benzoxazin-4-one.
January 1982, Die Pharmazie,
F De Marchi, and G F Tamagnone, and M V Torielli
Novel potassium channel activators. III. Synthesis and pharmacological evaluation of 3,4-dihydro-2H-1,4-benzoxazine derivatives: modification at the 2 position.
March 2000, Chemical & pharmaceutical bulletin,
Copied contents to your clipboard!