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Jean-Philippe Monserrat

Showing results (1-10 of 6) with videos related to

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Chemical Communications (Cambridge, England)|March 27, 2015
Exploring hydrogen peroxide responsive thiazolidinone-based prodrugsChristian Perez, Jean-Philippe Monserrat, Yao Chen, et al.
European Journal of Medicinal Chemistry|March 20, 2024
Progress on synthesis and structure-activity relationships of lamellarins over the past decadeMingze Wei, Jing Chen, Yuliang Song, et al.
Chemical Communications (Cambridge, England)|June 18, 2010
Synthesis of cytotoxic ferrocenyl flavones via a ferricenium-mediated 1,6-oxidative cyclizationJean-Philippe Monserrat, Guy G Chabot, Louis Hamon, et al.
European Journal of Medicinal Chemistry|October 5, 2025
Design, synthesis and bioactive evaluation of novel quinoline-linked sulfonamide-pyridine derivatives as PI3K/HDAC dual-target inhibitorsJinyu Sun, Jing Chen, Yijie Lou, et al.
Dalton Transactions (Cambridge, England : 2003)|January 14, 2012
In vitro inhibitory properties of ferrocene-substituted chalcones and aurones on bacterial and human cell culturesKeshri Nath Tiwari, Jean-Philippe Monserrat, Arnaud Hequet, et al.
Bioorganic & Medicinal Chemistry Letters|September 6, 2011
Ferrocenyl chalcone difluoridoborates inhibit HIV-1 integrase and display low activity towards cancer and endothelial cellsJean-Philippe Monserrat, Rasha I Al-Safi, Keshri Nath Tiwari, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Chemical Communications (Cambridge, England)|March 27, 2015
Exploring hydrogen peroxide responsive thiazolidinone-based prodrugsChristian Perez, Jean-Philippe Monserrat, Yao Chen, et al.
European Journal of Medicinal Chemistry|March 20, 2024
Progress on synthesis and structure-activity relationships of lamellarins over the past decadeMingze Wei, Jing Chen, Yuliang Song, et al.
Chemical Communications (Cambridge, England)|June 18, 2010
Synthesis of cytotoxic ferrocenyl flavones via a ferricenium-mediated 1,6-oxidative cyclizationJean-Philippe Monserrat, Guy G Chabot, Louis Hamon, et al.
European Journal of Medicinal Chemistry|October 5, 2025
Design, synthesis and bioactive evaluation of novel quinoline-linked sulfonamide-pyridine derivatives as PI3K/HDAC dual-target inhibitorsJinyu Sun, Jing Chen, Yijie Lou, et al.
Dalton Transactions (Cambridge, England : 2003)|January 14, 2012
In vitro inhibitory properties of ferrocene-substituted chalcones and aurones on bacterial and human cell culturesKeshri Nath Tiwari, Jean-Philippe Monserrat, Arnaud Hequet, et al.
Bioorganic & Medicinal Chemistry Letters|September 6, 2011
Ferrocenyl chalcone difluoridoborates inhibit HIV-1 integrase and display low activity towards cancer and endothelial cellsJean-Philippe Monserrat, Rasha I Al-Safi, Keshri Nath Tiwari, et al.
Pageof 1