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Synthesis, in vitro antimicrobial and in vivo antitumor evaluation of novel pyrimidoquinolines and its nucleoside derivatives.
Abbas, Hebat-Allah S; Hafez, Hend N; El-Gazzar, Abdel-Rahman B A.
Affiliation
  • Abbas HA; Photochemistry Department, National Research Centre, 12622 Dokki, Cairo, Egypt. hebanrc@yahoo.com
Eur J Med Chem ; 46(1): 21-30, 2011 Jan.
Article in En | MEDLINE | ID: mdl-21074295
Seven series of pyrimidoquinoline derivatives have been synthesized, tetrazolo[4',3':-1,2]pyrimido[4,5-b]quinoline (3), 2-aminopyrimido[4,5-b]quinoline (4), triazolo[4',3':1,2]-pyrimidoquinoline (5a,b, 10), imidazolo[3',2':1,2]pyrimido[4,5-b]-quinoline (8a,b), 6-chloro-2-methylthiopyrimido[4,5-b]quinoline (12), acetylated nucleosides (16, 17a,b) and deacetylated nucleosides (18, 19a,b). Some of the novel pyrimidoquinoline derivatives possess highly activity toward the bacteria and fungi species. The new quinolines derivatives were evaluated for their anticancer activity toward human cancer cell lines by the National Cancer Institute (NCI). Most of them had excellent growth inhibition activity, having LD(50) values in the low micromolar to nanomolar concentration range.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quinolines / Anti-Infective Agents / Antineoplastic Agents / Nucleosides Limits: Animals / Humans / Male Language: En Journal: Eur J Med Chem Year: 2011 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quinolines / Anti-Infective Agents / Antineoplastic Agents / Nucleosides Limits: Animals / Humans / Male Language: En Journal: Eur J Med Chem Year: 2011 Document type: Article Affiliation country: Country of publication: