Iron Chelators of the Di-2-pyridylketone Thiosemicarbazone and 2-Benzoylpyridine Thiosemicarbazone Series Inhibit HIV-1 Transcription: Identification of Novel Cellular Targets—Iron, Cyclin-Dependent Kinase (CDK) 2, and CDK9-Reference-Cited by-同舟云学术

Iron Chelators of the Di-2-pyridylketone Thiosemicarbazone and 2-Benzoylpyridine Thiosemicarbazone Series Inhibit HIV-1 Transcription: Identification of Novel Cellular Targets—Iron, Cyclin-Dependent Kinase (CDK) 2, and CDK9

Published:2010-10-18 Issue:1 Volume:79 Page:185-196
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Debebe Zufan,Ammosova Tatyana,Breuer Denitra,Lovejoy David B.,Kalinowski Danuta S.,Karla Pradeep K.,Kumar Krishna,Jerebtsova Marina,Ray Patricio,Kashanchi Fatah,Gordeuk Victor R.,Richardson Des R.,Nekhai Sergei

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference40 articles.

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4. Identification of the di-pyridyl ketone isonicotinoyl hydrazone (PKIH) analogues as potent iron chelators and anti-tumour agents

5. Cdk2 Knockout Mice Are Viable

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