Synthesis and biological activity of some methoctramine-related tetraamines bearing a 11-acetyl-5,11-dihydro-6H-pyrido[2,3-b][1,4]-benzodiazepin-6-one moiety as antimuscarinics: a second generation of highly selective M2 muscarinic receptor antagonists. 1993

C Melchiorre, and M L Bolognesi, and A Chiarini, and A Minarini, and S Spampinato
Department of Pharmaceutical Sciences, University of Bologna, Italy.

UI MeSH Term Description Entries
D011976 Receptors, Muscarinic One of the two major classes of cholinergic receptors. Muscarinic receptors were originally defined by their preference for MUSCARINE over NICOTINE. There are several subtypes (usually M1, M2, M3....) that are characterized by their cellular actions, pharmacology, and molecular biology. Muscarinic Acetylcholine Receptors,Muscarinic Receptors,Muscarinic Acetylcholine Receptor,Muscarinic Receptor,Acetylcholine Receptor, Muscarinic,Acetylcholine Receptors, Muscarinic,Receptor, Muscarinic,Receptor, Muscarinic Acetylcholine,Receptors, Muscarinic Acetylcholine
D003959 Diamines Organic chemicals which have two amino groups in an aliphatic chain. Diamine
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
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
D001569 Benzodiazepines A group of two-ring heterocyclic compounds consisting of a benzene ring fused to a diazepine ring. Benzodiazepine,Benzodiazepine Compounds
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
D015394 Molecular Structure The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds. Structure, Molecular,Molecular Structures,Structures, Molecular
D051381 Rats The common name for the genus Rattus. Rattus,Rats, Laboratory,Rats, Norway,Rattus norvegicus,Laboratory Rat,Laboratory Rats,Norway Rat,Norway Rats,Rat,Rat, Laboratory,Rat, Norway,norvegicus, Rattus
D018727 Muscarinic Antagonists Drugs that bind to but do not activate MUSCARINIC RECEPTORS, thereby blocking the actions of endogenous ACETYLCHOLINE or exogenous agonists. Muscarinic antagonists have widespread effects including actions on the iris and ciliary muscle of the eye, the heart and blood vessels, secretions of the respiratory tract, GI system, and salivary glands, GI motility, urinary bladder tone, and the central nervous system. Antimuscarinic,Antimuscarinic Agent,Antimuscarinic Agents,Cholinergic Muscarinic Antagonist,Muscarinic Antagonist,Antimuscarinics,Cholinergic Muscarinic Antagonists,Agent, Antimuscarinic,Agents, Antimuscarinic,Antagonist, Cholinergic Muscarinic,Antagonist, Muscarinic,Antagonists, Cholinergic Muscarinic,Antagonists, Muscarinic,Muscarinic Antagonist, Cholinergic,Muscarinic Antagonists, Cholinergic

Related Publications

C Melchiorre, and M L Bolognesi, and A Chiarini, and A Minarini, and S Spampinato
September 1997, Chemical & pharmaceutical bulletin,
C Melchiorre, and M L Bolognesi, and A Chiarini, and A Minarini, and S Spampinato
June 1997, Chemical & pharmaceutical bulletin,
C Melchiorre, and M L Bolognesi, and A Chiarini, and A Minarini, and S Spampinato
December 1982, Il Farmaco; edizione scientifica,
C Melchiorre, and M L Bolognesi, and A Chiarini, and A Minarini, and S Spampinato
October 1999, Bioorganic & medicinal chemistry letters,
C Melchiorre, and M L Bolognesi, and A Chiarini, and A Minarini, and S Spampinato
May 2015, Acta crystallographica. Section E, Crystallographic communications,
C Melchiorre, and M L Bolognesi, and A Chiarini, and A Minarini, and S Spampinato
January 1995, Life sciences,
C Melchiorre, and M L Bolognesi, and A Chiarini, and A Minarini, and S Spampinato
January 1993, Journal of medicinal chemistry,
C Melchiorre, and M L Bolognesi, and A Chiarini, and A Minarini, and S Spampinato
April 1975, Il Farmaco; edizione scientifica,
C Melchiorre, and M L Bolognesi, and A Chiarini, and A Minarini, and S Spampinato
September 2012, Journal of medicinal chemistry,
C Melchiorre, and M L Bolognesi, and A Chiarini, and A Minarini, and S Spampinato
July 2020, Journal of medicinal chemistry,
Copied contents to your clipboard!