Synthesis and in vitro cytotoxicity of 6-vinyluridine and related compounds Journal Article


Authors: Megati, S.; Sodum, R.; Otter, G. M.; Klein, R. S.; Otter, B. A.
Article Title: Synthesis and in vitro cytotoxicity of 6-vinyluridine and related compounds
Abstract: The 6-alkenyluracil nucleosides (7a-e) and bases (14a-i) were synthesized and evaluated for their ability to inhibit the growth of mouse leukemia L1210 cells in vitro. While several of the free bases are cytotoxic, with IC50 values in the 1 - 5 μM range, the corresponding β-d-ribofuranosyl nucleosides are not significantly active. © 1994.
Keywords: controlled study; unclassified drug; nonhuman; animal cell; mouse; cytotoxicity; drug structure; drug synthesis; structure activity relation; nucleoside; enantiomer; uridine derivative; article; ultraviolet spectrophotometry; leukemia l 1210; 6 vinyluracil; 6 vinyluridine
Journal Title: Bioorganic & Medicinal Chemistry Letters
Volume: 4
Issue: 3
ISSN: 0960-894X
Publisher: Pergamon-Elsevier Science Ltd  
Date Published: 1994-02-10
Start Page: 469
End Page: 472
Language: English
DOI: 10.1016/0960-894x(94)80018-9
PROVIDER: scopus
DOI/URL:
Notes: Export Date: 14 January 2019 -- Article -- Source: Scopus
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  1. Glenys M. Otter
    27 Otter