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Non-peptidic small molecule inhibitors of XIAP

Author
PARK, Cheol-Min1 ; CHAOHONG SUN2 ; OLEJNICZAK, Edward T2 ; WILSON, Alan E1 ; MEADOWS, Robert P2 ; BETZ, Stephen F2 ; ELMORE, Steven W1 ; FESIK, Stephen W1
[1] Cancer Research, Global Pharmaceutical R&D, Abbott Laboratories, 100 Abbott Park Rd, Abbott Park, IL 60064-6010, United States
[2] Advanced Technology, Global Pharmaceutical R&D, Abbott Laboratories, 100 Abbott Park Rd, Abbott Park, IL 60064-6010, United States
Source

Bioorganic & medicinal chemistry letters (Print). 2005, Vol 15, Num 3, pp 771-775, 5 p

ISSN
0960-894X
Scientific domain
Biochemistry, molecular biology, biophysics; Pharmacology drugs
Publisher
Elsevier, Oxford
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Anticancéreux Apoptose Composé non peptide Imidazole dérivé In vitro Inhibiteur Mimétique Relation structure activité Synthèse chimique Thiazole dérivé Protéine SMAC Protéine inhibition apoptose Thiazole(2-alanylamino-4-[4-bromophényl]-5-phényl)
Keyword (en)
Antineoplastic agent Apoptosis Non peptide compound Imidazole derivatives In vitro Inhibitor Mimetic Structure activity relation Chemical synthesis Thiazole derivatives Second mitochondria derived activator of caspase protein Apoptosis inhibitory protein
Keyword (es)
Anticanceroso Apoptosis Compuesto no péptido Imidazol derivado In vitro Inhibidor Mimético Relación estructura actividad Síntesis química Tiazol derivado
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
16478220

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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