Search Results - "Remiszewski, Stacy W."
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Psammaplins from the Sponge Pseudoceratina purpurea: Inhibition of Both Histone Deacetylase and DNA Methyltransferase
Published in Journal of organic chemistry (16-05-2003)“…Four novel bisulfide bromotyrosine derivatives, psammaplins E (9), F (10), G (11), and H (12), and two new bromotyrosine derivatives, psammaplins I (13) and J…”
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2
Inhibitors of Human Histone Deacetylase: Synthesis and Enzyme and Cellular Activity of Straight Chain Hydroxamates
Published in Journal of medicinal chemistry (14-02-2002)“…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…”
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3
Benzazepinones and Benzoxazepinones as Antagonists of Inhibitor of Apoptosis Proteins (IAPs) Selective for the Second Baculovirus IAP Repeat (BIR2) Domain
Published in Journal of medicinal chemistry (24-10-2013)“…XIAP is a key regulator of apoptosis, and its overexpression in cancer cells may contribute to their survival. The antiapoptotic function of XIAP derives from…”
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Optimization of Benzodiazepinones as Selective Inhibitors of the X‑Linked Inhibitor of Apoptosis Protein (XIAP) Second Baculovirus IAP Repeat (BIR2) Domain
Published in Journal of medicinal chemistry (24-10-2013)“…The IAPs are key regulators of the apoptotic pathways and are commonly overexpressed in many cancer cells. IAPs contain one to three BIR domains that are…”
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5
The discovery of NVP-LAQ824: from concept to clinic
Published in Current medicinal chemistry (01-11-2003)“…The natural products trapoxin B and trichostatin A, as well as the novel marine natural product psammaplin A (PSMA) were found in a cell-based screen for…”
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N-Hydroxy-3-phenyl-2-propenamides as Novel Inhibitors of Human Histone Deacetylase with in Vivo Antitumor Activity: Discovery of (2E)-N-Hydroxy-3-[4-[[(2-hydroxyethyl)[2-(1H-indol-3-yl)ethyl]amino]methyl]phenyl]-2-propenamide (NVP-LAQ824)
Published in Journal of medicinal chemistry (09-10-2003)“…A series of N-hydroxy-3-phenyl-2-propenamides were prepared as novel inhibitors of human histone deacetylase (HDAC). These compounds were potent enzyme…”
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7
Psammaplins from the Sponge Pseudoceratina p urpurea: Inhibition of Both Histone Deacetylase and DNA Methyltransferase
Published in Journal of organic chemistry (16-05-2003)“…Four novel bisulfide bromotyrosine derivatives, psammaplins E (9), F (10), G (11), and H (12), and two new bromotyrosine derivatives, psammaplins I (13) and J…”
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8
Total synthesis of the latrunculins
Published in Journal of the American Chemical Society (01-04-1992)Get full text
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9
Recent advances in the discovery of small molecule histone deacetylase inhibitors
Published in Current opinion in drug discovery & development (01-07-2002)“…The reversible acetylation of lysine amino groups in nuclear histones is an important mechanism by which gene expression is regulated, and may act by…”
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10
Synthesis of 5-epi-desosamine via a stereoselective intramolecular N-sulfinyl Diels-Alder cycloaddition
Published in Journal of organic chemistry (01-08-1984)Get full text
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11
N-hydroxy-3-phenyl-2-propenamides as novel inhibitors of human histone deacetylase with in vivo antitumor activity: Discovery of (2E)-N-hydroxy-3-[4-[[(2-hydroxyethyl)[2-(1H-indol-3-yl)ethyl]amino]methyl]-phen yl]-2-propenamide (NVP-LAQ824)
Published in Journal of medicinal chemistry (2003)Get full text
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12
Total synthesis of (+)-latrunculin A
Published in Journal of organic chemistry (01-06-1990)Get full text
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