1149-15-1Relevant academic research and scientific papers
The [(Cp)M(CO)3] (M=Re, 99mTc) building block for imaging agents and bioinorganic probes: Perspectives and limitations
Can, Daniel,Peindy N'Dongo, Harmel W.,Spingler, Bernhard,Schmutz, Paul,Alberto, Roger,Raposinho, Paula,Santos, Isabel
, p. 1849 - 1866,18 (2020/08/24)
Starting from asymmetric Thiele's acid derivatives, two different imaging probes [99mTc(CO)3(CpR)] (R=potential targeting vector) are generated simultaneously in one-pot and from one substrate. This extends the previously introduced
Inhibitors of human histone deacetylase: Synthesis and enzyme and cellular activity of straight chain hydroxamates
Remiszewski, Stacy W.,Sambucetti, Lidia C.,Atadja, Peter,Bair, Kenneth W.,Cornell, Wendy D.,Green, Michael A.,Howell, Kobporn Lulu,Jung, Manfred,Kwon, Paul,Trogani, Nancy,Walker, Heather
, p. 753 - 757 (2007/10/03)
Inhibitors of histone deacetylase (HDAC) have been shown to induce terminal differentiation of human tumor cell lines and to have antitumor effects in vivo. We have prepared analogues of suberoylanilide hydroxamic acid (SAHA) and trichostatin A and have evaluated them in a human HDAC enzyme inhibition assay, a p21waf1 (p21) promoter assay, and in monolayer growth inhibition assays. One compound, 4-(dimethylamino)-N-[7-(hydroxyamino)-7-oxoheptyl]-benzamide, was found to affect the growth of a panel of eight human tumor cell lines differentially.
