Indolizine derivatives with biological activity I: N'-substituted hydrazides of indolizine-2-carboxylic acid. 1977

M Cardellini, and F Claudi, and M Grifantini, and U Gulini, and S Martelli

The synthesis and antimonoamine oxidase activity of some N'-substituted hydrazides of indolizine-2-carboxylic acid are described. They all inhibit monoamine oxidase and are more active than iproniazid. The structure-activity relationships also are discussed.

UI MeSH Term Description Entries
D007212 Indolizines
D007490 Iproniazid An irreversible inhibitor of monoamine oxidase types A and B that is used as an antidepressive agent. It has also been used as an antitubercular agent, but its use is limited by its toxicity. Iprazid
D008996 Monoamine Oxidase Inhibitors A chemically heterogeneous group of drugs that have in common the ability to block oxidative deamination of naturally occurring monoamines. (From Gilman, et al., Goodman and Gilman's The Pharmacological Basis of Therapeutics, 8th ed, p414) MAO Inhibitor,MAO Inhibitors,Reversible Inhibitors of Monoamine Oxidase,Monoamine Oxidase Inhibitor,RIMA (Reversible Inhibitor of Monoamine Oxidase A),Reversible Inhibitor of Monoamine Oxidase,Inhibitor, MAO,Inhibitor, Monoamine Oxidase,Inhibitors, MAO,Inhibitors, Monoamine Oxidase
D002264 Carboxylic Acids Organic compounds containing the carboxy group (-COOH). This group of compounds includes amino acids and fatty acids. Carboxylic acids can be saturated, unsaturated, or aromatic. Carboxylic Acid,Acid, Carboxylic,Acids, Carboxylic
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
D066298 In Vitro Techniques Methods to study reactions or processes taking place in an artificial environment outside the living organism. In Vitro Test,In Vitro Testing,In Vitro Tests,In Vitro as Topic,In Vitro,In Vitro Technique,In Vitro Testings,Technique, In Vitro,Techniques, In Vitro,Test, In Vitro,Testing, In Vitro,Testings, In Vitro,Tests, In Vitro,Vitro Testing, In

Related Publications

M Cardellini, and F Claudi, and M Grifantini, and U Gulini, and S Martelli
September 1977, Journal of pharmaceutical sciences,
M Cardellini, and F Claudi, and M Grifantini, and U Gulini, and S Martelli
January 1975, Hindustan antibiotics bulletin,
M Cardellini, and F Claudi, and M Grifantini, and U Gulini, and S Martelli
November 2003, Farmaco (Societa chimica italiana : 1989),
M Cardellini, and F Claudi, and M Grifantini, and U Gulini, and S Martelli
August 2010, Bioorganic & medicinal chemistry letters,
M Cardellini, and F Claudi, and M Grifantini, and U Gulini, and S Martelli
September 1979, Journal of medicinal chemistry,
M Cardellini, and F Claudi, and M Grifantini, and U Gulini, and S Martelli
May 2024, ChemSusChem,
M Cardellini, and F Claudi, and M Grifantini, and U Gulini, and S Martelli
March 1979, Journal of pharmaceutical sciences,
M Cardellini, and F Claudi, and M Grifantini, and U Gulini, and S Martelli
December 2019, Molecules (Basel, Switzerland),
M Cardellini, and F Claudi, and M Grifantini, and U Gulini, and S Martelli
May 2000, Bioorganic & medicinal chemistry,
M Cardellini, and F Claudi, and M Grifantini, and U Gulini, and S Martelli
June 1968, Acta poloniae pharmaceutica,
Copied contents to your clipboard!