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HKH40A

National Institutes of Health

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RTA 502

Papers overview

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2014
2014
Abstract 1231:In vitroanticancer activity of imidazo-acridinone (HKH40A) in panels of human patient-derived tumor xenografts (PDXs) and human leukemia and lymphoma cell lines
Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA HKH40A is a synthetic, DNA-intercalating (Kosakowska… 
2009
2009
Involvement of ATM‐mediated Chk1/2 and JNK kinase signaling activation in HKH40A‐induced cell growth inhibition
HKH40A (RTA 502), or 5‐nitro‐2‐(3‐{4‐[3‐(8‐methoxy‐6‐oxo‐6H‐2,10b‐diaza‐aceanthrylen‐5‐ylamino)propyl]piperazin‐1‐yl}‐propyl)‐2… 
2009
2009
Growth inhibition of hepatocellular carcinoma cells in vitro and in vivo by the 8-methoxy analog of WMC79
HKH40A (RTA 502), an optimized 8-methoxy analog of the unsymmetrical bifunctional antitumor agent WMC79, was found to be potently… 
2007
2007
Optimization of naphthalimide-imidazoacridone with potent antitumor activity leading to clinical candidate (HKH40A, RTA 502).
Unsymmetrical bifunctional antitumor agent WMC79 was further optimized to generate compound 7b that not only inhibited the growth… 
2006
2006
288 POSTER Selective targeting of critical components of DNA replication by HKH40A (RTA 502)
2004
2004
549 HKH40A, potent agent agaist GI cancers, targets p53 or when that is mutated, Akt
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