Barnes, Griffin Magann, Nicholas Perrotta, Daniele Hörmann, Fabian Fernandez, Sebastian Vydyam, Pratap Choi, Jae-Yeon Prudhomme, Jacques Neal, Armund Le Roch, Karine
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On the basis of a streamlined route to the pyrroloiminoquinone (PIQ) core, we made 16 natural products spread across four classes of biosynthetically related alkaloid natural products, and multiple structural analogs, all in ≤8 steps longest linear sequence (LLS). The strategy features a Larock indole synthesis as the key operation in a five-step s...
Roth, Patrick Gorlia, Thierry Reijneveld, Jaap C de Vos, Filip Idbaih, Ahmed Frenel, Jean-Sébastien Le Rhun, Emilie Sepulveda, Juan Manuel Perry, James Masucci, G Laura
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BackgroundStandard treatment for patients with newly diagnosed glioblastoma includes surgery, radiotherapy (RT), and temozolomide (TMZ) chemotherapy (TMZ/RT→TMZ). The proteasome has long been considered a promising therapeutic target because of its role as a central biological hub in tumor cells. Marizomib is a novel pan-proteasome inhibitor that c...
Roth, Patrick Gorlia, Thierry Reijneveld, Jaap C de Vos, Filip Idbaih, Ahmed Frenel, Jean-Sébastien Le Rhun, Emilie Sepulveda, Juan Manuel Perry, James Masucci, G Laura
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peer reviewed / [en] BACKGROUND: Standard treatment for patients with newly diagnosed glioblastoma includes surgery, radiotherapy (RT), and temozolomide (TMZ) chemotherapy (TMZ/RT→TMZ). The proteasome has long been considered a promising therapeutic target because of its role as a central biological hub in tumor cells. Marizomib is a novel pan-prot...
Kadiyala, Gayatri Nikhila Telwatte, Sushama Wedrychowski, Adam Janssens, Julie Kim, Sun Jin Kim, Peggy Deeks, Steven Wong, Joseph K Yukl, Steven A
ObjectivesSome drugs that augment cell-intrinsic defenses or modulate cell death/survival pathways have been reported to selectively kill cells infected with HIV or Simian Immunodeficiency Virus (SIV), but comparative studies are lacking. We hypothesized that these drugs may differ in their ability to kill cells infected with intact and defective p...
Necchi, A.; Pouessel, D.; Leibowitz, R.; Gupta, S.; Flechon, A.; Garcia-Donas, J.; Bilen, M.A.; Debruyne, P.R.; 49760; Milowsky, M.I.; Friedlander, T.;
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BACKGROUND: Fibroblast growth factor receptor 3 (FGFR3) alterations are oncogenic drivers of urothelial carcinoma (UC). Pemigatinib is a selective, oral inhibitor of FGFR1-3 with antitumor activity. We report the efficacy and safety of pemigatinib in the open-label, single-arm, phase II study of previously treated, unresectable or metastatic UC wit...
Chen, Kunpeng Mayorga, Raphael Hamilton, Caitlin Bahreini, Roya Lin, Ying-Hsuan Zhang, Haofei
The light absorption properties of brown carbon (BrC), which are linked to molecular chromophores, may play a significant role in the Earths energy budget. While nitroaromatic compounds have been identified as strong chromophores in wildfire-driven BrC, other types of chromophores remain to be investigated. Given the electron-withdrawing nature of ...
Cosaro, Emma Pires, Jully Castillo, Diego Murphy, Brian Reagan, Krystle
Nucleoside analogs GS-441524 and remdesivir (GS-5734) are effective in treating cats with feline infectious peritonitis (FIP). However, no studies have compared the efficacy between antiviral medications. The objective of this study was to evaluate the efficacy of orally administered GS-442514 (12.5-15 mg/kg) compared to orally administered remdesi...
Droege, Daniel G Parker, A Leila Milligan, Griffin M Jenkins, Robert Johnstone, Timothy C
Herein we report an investigation into the synthesis, metalation, and functionalization of bis-pocket porphyrins using the Suzuki-Miyaura cross-coupling reaction. Steric limitations to accessing bis-pocket porphyrins were overcome by using this Pd-catalyzed C-C-bond-forming strategy to introduce steric bulk after macrocyclization: 2,6-dibromo-4-tri...
Wagh, Sachin B. Maslivetc, Vladimir La Clair, James J. Kornienko, Alexander
Published in
Tetrahedron
Muńko, Malwina Ciesielska, Karolina Pluskota-Karwatka, Donata
Published in
Bioorganic chemistry
Furan is an environmental pollutant also present in heat-treated food. The compound is toxic and carcinogenic to rats, and classified as a possible human carcinogen. Mechanisms laying behind the furan carcinogenicity remain unclear, however scientific data indicate the involvement of bioactivation catalysed by cytochrome P450 2E1. The resulted init...