BIOMAT Database Logo BIOMAT Database Logo

[Synthesis of 2,3-diazaphenothiazines. XIV. Dialkylaminoalkyl derivatives of 8-acetylamino-2H-pyridazino(4,5b)(1,4)benzothiazine-1(10H)-one and of the isomer 8-acetylamino-3H-pyridazino(4,5b)(1,4)benzothiazine-4(10H)-one]. 1978

F Duro, and F Pappalardo, and F Vittorio

A description is given of some 2 or 3 dialkylaminoalkyl derivatives of 8-acetylamino-2H-pyridazino[4,5-b][1,4]benzothiazin-1(10H)-one (IV a...d) and 8-acetylamino-3H-pyridazino[4,5-b][1,4]benzothiazin-4(10H)-one (VIII a...d). The derivatives were subjected to pharmacological examination.

UI MeSH Term Description Entries
D008722 Methods A series of steps taken in order to conduct research. Techniques,Methodological Studies,Methodological Study,Procedures,Studies, Methodological,Study, Methodological,Method,Procedure,Technique
D010640 Phenothiazines Compounds containing dibenzo-1,4-thiazine. Some of them are neuroactive.
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
D001372 Aza Compounds Organic chemicals where carbon atoms have been replaced by nitrogen atoms. Compounds, Aza
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 Duro, and F Pappalardo, and F Vittorio
Synthesis and pharmacological evaluation of 3H-pyridazino[4,5-b][1,4]benzothiazin-4(10H)-one derivatives.
April 1994, Farmaco (Societa chimica italiana : 1989),
F Duro, and F Pappalardo, and F Vittorio
Chemical and pharmacological investigations on 2H-pyridazino[4,5-b] [1,4]benzothiazin-1(10H)-one derivatives.
October 1989, Farmaco (Societa chimica italiana : 1989),
F Duro, and F Pappalardo, and F Vittorio
Inhibitors of adhesion molecules expression; the synthesis and pharmacological properties of 10H-pyrazino[2,3-b][1,4]benzothiazine derivatives.
July 2002, Chemical & pharmaceutical bulletin,
F Duro, and F Pappalardo, and F Vittorio
Synthesis of new derivatives of 4-hydroxy-(2H)-phthalazinone and phthalazino-1,4-(2H)(3H)-dione.
January 1992, Acta poloniae pharmaceutica,
F Duro, and F Pappalardo, and F Vittorio
Piperidine carboxylic acid derivatives of 10H-pyrazino[2,3-b][1,4]benzothiazine as orally-active adhesion molecule inhibitors.
June 2004, Chemical & pharmaceutical bulletin,
F Duro, and F Pappalardo, and F Vittorio
Pyridazine derivatives. X. 10H-benzo[b]pyridazino[3,4-e][1,4]thiazine and 5H-benzo[b]pyridazino[4,3-e][1,4]thiazine.
July 1966, Chemical & pharmaceutical bulletin,
F Duro, and F Pappalardo, and F Vittorio
[Pyridinol derivatives. (8) Synthesis and pharmacological activity of 4-phenylalkyl-2H-pyrido[3,2-b]-1,4-oxazin-3-one derivatives].
August 1983, Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan,
F Duro, and F Pappalardo, and F Vittorio
Synthesis and anthelmintic activity of benzopyrano[2,3-c]pyrazol-4(2H)-one derivatives.
November 2020, Molecular diversity,
F Duro, and F Pappalardo, and F Vittorio
Studies on the synthesis of pyridazine derivatives. IX. Synthesis of 10H-pyridazino(3,2-b)quinazolin-10-one and its derivatives. (3).
June 1968, Chemical & pharmaceutical bulletin,
F Duro, and F Pappalardo, and F Vittorio
[Research on 1,4-benzothiazines. IV. N-dialkylaminoalkyl derivatives of 2-carboethoxy- and 2-carbomethoxy-4H-1,4-benzothiazine].
August 1972, Il Farmaco; edizione scientifica,
Copied contents to your clipboard!