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Synthesis and potent antitumor activities of novel 1,3,5-cis, cis-triaminocyclohexane N-pyridyl derivatives

Author
CHONG, Hyun-Soon1 ; TORTI, Suzy V2 3 ; MA, Rong2 3 ; TORTI, Frank M3 4 ; BRECHBIEL, Martin W1
[1] Chemistry, Section, National Cancer Institute, NIH, Bethesda, Maryland, United States
[2] Department of Cancer Biology, Wake Forest University, Winston Salem, North Carolina, United States
[3] Comprehensive Cancer Center, Wake Forest University, Winston Salem, North Carolina, United States
[4] Department of Biochemistry, Wake Forest University, Winston Salem, North Carolina, United States
Source

Journal of medicinal chemistry (Print). 2004, Vol 47, Num 21, pp 5230-5234, 5 p ; ref : 14 ref

CODEN
JMCMAR
ISSN
0022-2623
Scientific domain
Pharmacology drugs
Publisher
American Chemical Society, Washington, DC
Publication country
United States
Document type
Article
Language
English
Keyword (fr)
Activité biologique Anticancéreux Chélateur Cyclohexane dérivé Fer In vitro Lignée HeLa Lignée cellulaire Pyridine dérivé Stéréoisomère cis Synthèse chimique Cyclohexane(1,3,5-tris[5-(3-[t-butoxycarbonylamino]propylcarbamoyl)-2-pyridylméthylamino])
Keyword (en)
Biological activity Antineoplastic agent Chelating agent Cyclohexane derivatives Iron In vitro Hela cell line Cell line Pyridine derivatives Cis stereoisomer Chemical synthesis
Keyword (es)
Actividad biológica Anticanceroso Quelante Ciclohexano derivado Hierro In vitro Célula HeLa Línea celular Piridina derivado Estereoisómero cis Síntesis química
Classification
Pascal
002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments / 002B02R Antineoplastic agents / 002B02R01 General aspects

Discipline
Pharmacological treatments
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
16200657

Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS

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