Synthesis and anti-tumor activities of N'-benzylidene-2-(4-oxothieno[2,3-d] pyrimidin-3(4H)-yl)acetohydrazone derivatives
- Autor
- JIANGPING LOU1 ; ZHEN LIU2 ; YAN LI2 ; MI ZHOU2 ; ZHENGXI ZHANG2 ; SHU ZHENG1 ; RENXIAO WANG2 ; JIAN LI1
[1] School of Pharmacy, East China University of Science and Technology, 130 Mei Long Road, Shanghai 200237, China
[2] State Key Laboratory of Bioorganic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China - Fuente
Bioorganic & medicinal chemistry letters (Print). 2011, Vol 21, Num 22, pp 6662-6666, 5 p ; ref : 16 ref
- ISSN
- 0960-894X
- Campo Científico
- Biochemistry, molecular biology, biophysics; Pharmacology drugs
- Editor
- Elsevier, Amsterdam
- País de la publicación
- Netherlands
- Tipo de documento
- Article
- Idioma
- English
- Palabra clave de autor
- Acetohydrazone Anti-tumor compound Apoptosis inducer Cytotoxicity Thienopyrimidine
- Palabra clave (fr)
- Activité biologique Anticancéreux Apoptose Cytotoxicité Dérivé de la pyrimidine Mort cellulaire Synthèse chimique Thiénopyrimidine
- Palabra clave (in)
- Biological activity Antineoplastic agent Apoptosis Cytotoxicity Pyrimidine derivatives Cell death Chemical synthesis
- Palabra clave (es)
- Actividad biológica Anticanceroso Apoptosis Citotoxicidad Pirimidina derivado Muerte celular Síntesis química
- Clasificación
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B02 Pharmacology. Drug treatments
- Disciplina
- General pharmacology
- Procedencia
- Inist-CNRS
- Base de datos
- PASCAL
- Identificador INIST
- 25589630
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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DOI
10.1016/j.bmcl.2011.09.061 
https://dx.doi.org/10.1016/j.bmcl.2011.09.061
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