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Quinoxaline chemistry. Part 4. 2(R)-anilinoquinoxalines as nonclassical antifolate agents. Synthesis, structure elucidation and evaluation of in vitro anticancer activity.
Loriga, M; Fiore, M; Sanna, P; Paglietti, G.
Affiliation
  • Loriga M; Istituto di Chimica Farmaceutica, Università di Sassari.
Farmaco ; 50(5): 289-301, 1995 May.
Article in En | MEDLINE | ID: mdl-7626163
ABSTRACT
Thirty-five quinoxalines bearing a substituted aniline group on position 2 and various substituents on positions 3,6,7 and 8 were prepared in order to evaluate in vitro anticancer activity. Structural elucidation of some isomeric quinoxalinones formed by ring closure of 4-substituted-1,2-diaminobenzenes with dicarbonyl compounds was achieved by comparison with one isomer coming from an unambiguous independent route. Preliminary in vitro screening at NCI showed that many compounds exhibited a moderate to strong growth inhibition activity on various cell lines between 10(-5) and 10(-4) molar concentrations.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Quinoxalines / Folic Acid Antagonists Limits: Humans Language: En Journal: Farmaco Journal subject: FARMACOLOGIA / QUIMICA Year: 1995 Type: Article
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Collection: 01-internacional Database: MEDLINE Main subject: Quinoxalines / Folic Acid Antagonists Limits: Humans Language: En Journal: Farmaco Journal subject: FARMACOLOGIA / QUIMICA Year: 1995 Type: Article