Synthesis and evaluation of cytotoxic activity of novel arylsulfonylimidazolidinones

DOI: 10.1016/0960-894X(96)00463-5

Source and publish data:

Bioorganic and Medicinal Chemistry Letters p. 2553 - 2558 (1996)

Update date:2022-08-04

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Authors:

Jung, Sang-Hun

Song, Jae-Shin

Lee, Hui-Soon

Choi, Sang-Un

Lee, Chong-Ock

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Article abstract of DOI:10.1016/0960-894X(96)00463-5

Synthesis of novel arylsulfonylimidazolidinones 3 and 4 containing sulfonylurea pharmacophore and evaluation of their in vitro cytotoxicity against human cell lines were investigated. As a result, a series of 4-phenyl-1(N)-arylsulfonylimidazolidinones have been found to be the potential anticancer agent.

Full text of DOI:10.1016/0960-894X(96)00463-5

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Article Doi

Synthesis and evaluation of cytotoxic activity of novel arylsulfonylimidazolidinones

DOI: 10.1016/0960-894X(96)00463-5

Source and publish data:

Authors:

Article abstract of DOI:10.1016/0960-894X(96)00463-5

Full text of DOI:10.1016/0960-894X(96)00463-5

Products guided by the article

R&D Labs maybe for 185098-56-0

Relevant to this article

A scalemic synthesis of the scopadulcic acid skeleton. I: An efficient γ-alkylation at C-9 in abietane framework and subsequent aldol reaction

Utilization of 1-Aryl-2,2-dibromocyclopropanes in synthetic approaches to phenanthroquinolizidine and phenanthroindolizidine alkaloids

On Conformational Sensitivity in the Ultraviolet Spectra of Cyclopropyl Ketones and Olefins

&β-AMINO KETONES-SUBSTITUTED &α-AMINO ACIDS. II. N-<&β-(p-SUBSTITUTED BENZOYL)ETHYL>-D-&α-ALANINES, GLYCINES AND THEIR ETHYL ESTERS

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