Abstract
Halogenated diarylacetylenes that possess fluorine or chlorine substituents in one aryl ring and N-methylamino or N,N-dimethylamino in the other aryl ring inhibit the proliferation of LS174T colon cancer cells through the repression of c-myc expression and induction of the cyclin-dependent kinase inhibitor-1 (i.e., p21(Wif1/Cip1)) and represent potentially useful antineoplastic agents.
Original language | English |
---|---|
Pages (from-to) | 3638-3640 |
Number of pages | 3 |
Journal | Bioorganic and Medicinal Chemistry Letters |
Volume | 24 |
Issue number | 15 |
DOIs | |
State | Published - Aug 1 2014 |
Bibliographical note
Funding Information:C.L. and D.S.W. were supported by R21 CA139359 and CA172379 from the NIH . C.G.Z. was supported by CHE-1111761 from the NSF . D.S.W. was supported by the Office of the Dean of the College of Medicine and by NIH Grant Number P20 RR020171 from the National Institute of General Medical Sciences to L. Hersh, P.I. Its contents are solely the responsibility of the authors and do not necessarily represent the official views of the NIH or the NIGMS.
Keywords
- Antineoplastic agents
- Colon cancer
- Diarylacetylenes
- c-myc
ASJC Scopus subject areas
- Biochemistry
- Molecular Medicine
- Molecular Biology
- Pharmaceutical Science
- Drug Discovery
- Clinical Biochemistry
- Organic Chemistry