BIOMAT Database Logo BIOMAT Database Logo

Synthesis and some pharmacological activities of 4-alkylamino-2,3-dimethyl-l-phenyl-3-pyrazolin-5-one derivatives. 1971

F Banci, and M J Bulgini, and E Tubaro

UI MeSH Term Description Entries
D006993 Hypnotics and Sedatives Drugs used to induce drowsiness or sleep or to reduce psychological excitement or anxiety. Hypnotic,Sedative,Sedative and Hypnotic,Sedatives,Hypnotic Effect,Hypnotic Effects,Hypnotics,Sedative Effect,Sedative Effects,Sedatives and Hypnotics,Effect, Hypnotic,Effect, Sedative,Effects, Hypnotic,Effects, Sedative,Hypnotic and Sedative
D008297 Male Males
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
D011720 Pyrazoles Azoles of two nitrogens at the 1,2 positions, next to each other, in contrast with IMIDAZOLES in which they are at the 1,3 positions.
D002621 Chemistry A basic science concerned with the composition, structure, and properties of matter; and the reactions that occur between substances and the associated energy exchange.
D004357 Drug Synergism The action of a drug in promoting or enhancing the effectiveness of another drug. Drug Potentiation,Drug Augmentation,Augmentation, Drug,Augmentations, Drug,Drug Augmentations,Drug Potentiations,Drug Synergisms,Potentiation, Drug,Potentiations, Drug,Synergism, Drug,Synergisms, Drug
D005260 Female Females
D006168 Guinea Pigs A common name used for the genus Cavia. The most common species is Cavia porcellus which is the domesticated guinea pig used for pets and biomedical research. Cavia,Cavia porcellus,Guinea Pig,Pig, Guinea,Pigs, Guinea
D006591 Hexobarbital A barbiturate that is effective as a hypnotic and sedative. Evipan,Hexenal,Hexobarbitone,Sodium Hexobarbital,Hexobarbital, Sodium
D006634 Histamine H1 Antagonists Drugs that selectively bind to but do not activate histamine H1 receptors, thereby blocking the actions of endogenous histamine. Included here are the classical antihistaminics that antagonize or prevent the action of histamine mainly in immediate hypersensitivity. They act in the bronchi, capillaries, and some other smooth muscles, and are used to prevent or allay motion sickness, seasonal rhinitis, and allergic dermatitis and to induce somnolence. The effects of blocking central nervous system H1 receptors are not as well understood. Antihistamines, Classical,Antihistaminics, Classical,Antihistaminics, H1,Histamine H1 Antagonist,Histamine H1 Receptor Antagonist,Histamine H1 Receptor Antagonists,Histamine H1 Receptor Blockaders,Antagonists, Histamine H1,Antagonists, Histamine H1 Receptor,Antihistamines, Sedating,Blockaders, Histamine H1 Receptor,First Generation H1 Antagonists,H1 Receptor Blockaders,Histamine H1 Blockers,Receptor Blockaders, H1,Antagonist, Histamine H1,Classical Antihistamines,Classical Antihistaminics,H1 Antagonist, Histamine,H1 Antagonists, Histamine,H1 Antihistaminics,Sedating Antihistamines

Related Publications

F Banci, and M J Bulgini, and E Tubaro
[Sulfonamides. 9. Sulfonamide derivatives of 1-phenyl-3,5-dimethylpyrazolyl-4-carboxylic acid and 1-phenyl-2,3-dimethyl-pyrazolin-5-one-4-carboxylic acid].
January 1976, Die Pharmazie,
F Banci, and M J Bulgini, and E Tubaro
Copper(II) complexes with ligands derived from 4-amino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one: synthesis and biological activity.
November 2006, Molecules (Basel, Switzerland),
F Banci, and M J Bulgini, and E Tubaro
[Reactivity of 2, 3-dimethyl-1-phenyl-3-pyrazolin-5-one-4-aldehydes (antipyrine aldehyde-4)].
March 1956, Die Pharmazie,
F Banci, and M J Bulgini, and E Tubaro
[Photolysis of 4-amino-, 4-alkoxy- and 4-Hydroxy-2,3-dimethyl-1-phenyl-3-pyrazolin-5-ones (author's transl)].
March 1976, Archiv der Pharmazie,
F Banci, and M J Bulgini, and E Tubaro
Design, Synthesis, Spectral Analysis, In Vitro Anticancer Evaluation and Molecular Docking Studies of Some Fluorescent 4-Amino-2, 3-Dimethyl-1-Phenyl-3-Pyrazolin-5-One, Ampyrone Derivatives.
March 2017, Interdisciplinary sciences, computational life sciences,
F Banci, and M J Bulgini, and E Tubaro
Design, synthesis and the biological evaluation of new 1,3-thiazolidine-4-ones based on the 4-amino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one scaffold.
September 2014, Molecules (Basel, Switzerland),
F Banci, and M J Bulgini, and E Tubaro
Carcinogenic N-nitrosodimethylamine as a contamination in drugs containing 4-dimethylamino-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one (amidopyrine, aminophenazone).
January 1979, Arzneimittel-Forschung,
F Banci, and M J Bulgini, and E Tubaro
[Studies on 4-formylamino-2,3-dimethyl-1-phenyl-3-pyrazoline-5-one].
June 1973, Archiv der Pharmazie,
F Banci, and M J Bulgini, and E Tubaro
Reactions of 1,3-Diphenyl-2-pyrazolin-5-one and 4-Amino-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one. Synthesis of Some New Pyrazoles and Pyrazolones.
December 2010, Acta chimica Slovenica,
F Banci, and M J Bulgini, and E Tubaro
Synthesis and pharmacological evaluation of some 2,3-dihydro-3-phenyl-1,4-benzodioxin derivatives.
November 1981, Il Farmaco; edizione scientifica,
Copied contents to your clipboard!