Synthesis and Cytotoxic Evaluation of Novel 3-Substituted Derivatives of 2-Indolinone

AuthorShaya Mokhtarien
AuthorMahmoud Mosaddeghen
AuthorMaryam Hamzeloo Moghadamen
AuthorZohreh Soleymanien
AuthorSaeideh Ghafarien
AuthorFarzad Kobarfarden
Issued Date2012-04-30en
AbstractThe assessment of the degree or rate of cellular proliferation and cell viability is critical for the assessment of the effects of drugs on both normal and malignant cell populations. In the present study, a few novel 3-substituted derivatives of 2-indolinones were synthesized by condensation of substituted oxindole or isatin derivatives with appropriate aldehydes or primary aromatic amines respectively. The synthesized compounds were screened for their cytotoxicity against HT-29 (human colon adenocarcinoma cell line) and MCF-7 (human breast adenocarcinoma cell line) cells using short term cytotoxicity MTT assay protocol. A few derivatives with IC50 < 10 µM were identified among them. he compound bearing 5-bromo substitution was the most potent derivative. Global physicochemical properties for compounds IVa-e and Va-h were calculated and the two most active compounds (IVa and IVb) showed similar CLogP values.en
DOIhttps://doi.org/10.22037/ijpr.2012.1140en
Keyword3- substituted derivatives of 2-indolinonesen
KeywordIndole derivativesen
KeywordCytotoxicityen
KeywordColon and breast canceren
KeywordMTT assayen
PublisherBrieflandsen
TitleSynthesis and Cytotoxic Evaluation of Novel 3-Substituted Derivatives of 2-Indolinoneen
TypeOriginal Articleen

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