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Stephen Hanessian

Showing results (111-120 of 154) with videos related to

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Bioorganic & Medicinal Chemistry Letters|September 26, 2007
Omega-alkoxy analogues of SAHA (vorinostat) as inhibitors of HDAC: a study of chain-length and stereochemical dependenceStephen Hanessian, Luciana Auzzas, Giuseppe Giannini, et al.
Bioorganic & Medicinal Chemistry Letters|December 31, 2013
Design and synthesis of potential dual NK(1)/NK(3) receptor antagonistsStephen Hanessian, Vincent Babonneau, Nicolas Boyer, et al.
Bioorganic & Medicinal Chemistry Letters|April 13, 2007
Structure-based organic synthesis of unnatural aeruginosin hybrids as potent inhibitors of thrombinStephen Hanessian, Karolina Ersmark, Xiaotian Wang, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Vorinostat-like molecules as structural, stereochemical, and pharmacological toolsStephen Hanessian, Luciana Auzzas, Andreas Larsson, et al.
RSC Advances|July 29, 2024
Towards combining backbone and sugar constraint in 3'-3' bis-phosphonate tethered 2'-4' bridged LNA oligonucleotide trimersEdouard Duchamp, Guillermo Vasquez, Neda Firoozi, et al.
The Journal of Organic Chemistry|August 14, 2013
Synthesis of cis- and trans-α-l-[4.3.0]bicyclo-DNA monomers for antisense technology: methods for the diastereoselective formation of bicyclic nucleosidesStephen Hanessian, Benjamin R Schroeder, Bradley L Merner, et al.
European Journal of Medicinal Chemistry|October 8, 2018
In search of constrained FTY720 and phytosphingosine analogs as dual acting anticancer agents targeting metabolic and epigenetic pathwaysJean-Baptiste Garsi, Lorenzo Sernissi, Vito Vece, et al.
Organic & Biomolecular Chemistry|January 15, 2016
Design, synthesis, and duplex-stabilizing properties of conformationally constrained tricyclic analogues of LNARobert D Giacometti, Juan C Salinas, Michael E Østergaard, et al.
Bioorganic & Medicinal Chemistry Letters|November 18, 2005
Phenolic P2/P3 core motif as thrombin inhibitors--design, synthesis, and X-ray co-crystal structureStephen Hanessian, Eric Therrien, Willem A L van Otterlo, et al.
ACS Medicinal Chemistry Letters|July 14, 2026
Design and Synthesis of Phosphonoproline-Proline Bioisosteric Mimetics of Proline Dimers: Pseudopeptide Constructs as Potential Inhibitors of the Zn-Metalloprotease PPEP‑1 Associated with <i>Clostridioides difficile</i>Erick Ivan Martinez Toto, Sofiane Hocine, Jean-Baptiste Garsi, et al.
Pageof 16

Showing results (111-120 of 154) with videos related to

Sort By:
Pageof 16
Bioorganic & Medicinal Chemistry Letters|September 26, 2007
Omega-alkoxy analogues of SAHA (vorinostat) as inhibitors of HDAC: a study of chain-length and stereochemical dependenceStephen Hanessian, Luciana Auzzas, Giuseppe Giannini, et al.
Bioorganic & Medicinal Chemistry Letters|December 31, 2013
Design and synthesis of potential dual NK(1)/NK(3) receptor antagonistsStephen Hanessian, Vincent Babonneau, Nicolas Boyer, et al.
Bioorganic & Medicinal Chemistry Letters|April 13, 2007
Structure-based organic synthesis of unnatural aeruginosin hybrids as potent inhibitors of thrombinStephen Hanessian, Karolina Ersmark, Xiaotian Wang, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Vorinostat-like molecules as structural, stereochemical, and pharmacological toolsStephen Hanessian, Luciana Auzzas, Andreas Larsson, et al.
RSC Advances|July 29, 2024
Towards combining backbone and sugar constraint in 3'-3' bis-phosphonate tethered 2'-4' bridged LNA oligonucleotide trimersEdouard Duchamp, Guillermo Vasquez, Neda Firoozi, et al.
The Journal of Organic Chemistry|August 14, 2013
Synthesis of cis- and trans-α-l-[4.3.0]bicyclo-DNA monomers for antisense technology: methods for the diastereoselective formation of bicyclic nucleosidesStephen Hanessian, Benjamin R Schroeder, Bradley L Merner, et al.
European Journal of Medicinal Chemistry|October 8, 2018
In search of constrained FTY720 and phytosphingosine analogs as dual acting anticancer agents targeting metabolic and epigenetic pathwaysJean-Baptiste Garsi, Lorenzo Sernissi, Vito Vece, et al.
Organic & Biomolecular Chemistry|January 15, 2016
Design, synthesis, and duplex-stabilizing properties of conformationally constrained tricyclic analogues of LNARobert D Giacometti, Juan C Salinas, Michael E Østergaard, et al.
Bioorganic & Medicinal Chemistry Letters|November 18, 2005
Phenolic P2/P3 core motif as thrombin inhibitors--design, synthesis, and X-ray co-crystal structureStephen Hanessian, Eric Therrien, Willem A L van Otterlo, et al.
ACS Medicinal Chemistry Letters|July 14, 2026
Design and Synthesis of Phosphonoproline-Proline Bioisosteric Mimetics of Proline Dimers: Pseudopeptide Constructs as Potential Inhibitors of the Zn-Metalloprotease PPEP‑1 Associated with <i>Clostridioides difficile</i>Erick Ivan Martinez Toto, Sofiane Hocine, Jean-Baptiste Garsi, et al.
Pageof 16