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R Wexler

Showing results (321-330 of 418) with videos related to

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Bioorganic & Medicinal Chemistry Letters|March 4, 2000
The de novo design and synthesis of cyclic urea inhibitors of factor Xa: optimization of the S4 ligandR A Galemmo, B L Wells, K A Rossi, et al.
Journal of Medicinal Chemistry|December 2, 2021
Identification of a Hydroxypyrimidinone Compound (<b>21</b>) as a Potent APJ Receptor Agonist for the Potential Treatment of Heart FailureWei Meng, Zulan Pi, Robert Brigance, et al.
Bioorganic & Medicinal Chemistry Letters|April 3, 2021
Small molecule and macrocyclic pyrazole derived inhibitors of myeloperoxidase (MPO)Carol H Hu, Meriah W Neissel Valente, O Scott Halpern, et al.
Journal of Medicinal Chemistry|January 14, 2000
Isoxazolines as potent antagonists of the integrin alpha(v)beta(3)W J Pitts, J Wityak, J M Smallheer, et al.
ACS Medicinal Chemistry Letters|June 17, 2026
Solubility-Driven Lead Optimization of PAR4 Antagonists and Evaluation of a Phosphate Ester Prodrug Delivery StrategyO Scott Halpern, Samuel K Reznik, Xiaojun Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|January 27, 2010
Phenyltriazolinones as potent factor Xa inhibitorsMimi L Quan, Donald J P Pinto, Karen A Rossi, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Pyrazoles, 1,2,4-triazoles, and tetrazoles as surrogates for cis-amide bonds in boronate ester thrombin inhibitorsJ V Duncia, J B Santella, C A Higley, et al.
Bioorganic & Medicinal Chemistry Letters|November 26, 2013
Potent P2Y1 urea antagonists bearing various cyclic amine scaffoldsRéjean Ruel, Alexandre L'Heureux, Carl Thibeault, et al.
Bioorganic & Medicinal Chemistry Letters|September 11, 2016
Synthesis and P1' SAR exploration of potent macrocyclic tissue factor-factor VIIa inhibitorsVladimir Uladzimir Ladziata, Peter W Glunz, Yan Zou, et al.
Bioorganic & Medicinal Chemistry Letters|May 16, 2007
Design and synthesis of benzoazepinone-derived cyclic malonamides and aminoamides as potent gamma-secretase inhibitorsMichael G Yang, Jian-Liang Shi, Dilip P Modi, et al.
Pageof 42

Showing results (321-330 of 418) with videos related to

Sort By:
Pageof 42
Bioorganic & Medicinal Chemistry Letters|March 4, 2000
The de novo design and synthesis of cyclic urea inhibitors of factor Xa: optimization of the S4 ligandR A Galemmo, B L Wells, K A Rossi, et al.
Journal of Medicinal Chemistry|December 2, 2021
Identification of a Hydroxypyrimidinone Compound (<b>21</b>) as a Potent APJ Receptor Agonist for the Potential Treatment of Heart FailureWei Meng, Zulan Pi, Robert Brigance, et al.
Bioorganic & Medicinal Chemistry Letters|April 3, 2021
Small molecule and macrocyclic pyrazole derived inhibitors of myeloperoxidase (MPO)Carol H Hu, Meriah W Neissel Valente, O Scott Halpern, et al.
Journal of Medicinal Chemistry|January 14, 2000
Isoxazolines as potent antagonists of the integrin alpha(v)beta(3)W J Pitts, J Wityak, J M Smallheer, et al.
ACS Medicinal Chemistry Letters|June 17, 2026
Solubility-Driven Lead Optimization of PAR4 Antagonists and Evaluation of a Phosphate Ester Prodrug Delivery StrategyO Scott Halpern, Samuel K Reznik, Xiaojun Zhang, et al.
Bioorganic & Medicinal Chemistry Letters|January 27, 2010
Phenyltriazolinones as potent factor Xa inhibitorsMimi L Quan, Donald J P Pinto, Karen A Rossi, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Pyrazoles, 1,2,4-triazoles, and tetrazoles as surrogates for cis-amide bonds in boronate ester thrombin inhibitorsJ V Duncia, J B Santella, C A Higley, et al.
Bioorganic & Medicinal Chemistry Letters|November 26, 2013
Potent P2Y1 urea antagonists bearing various cyclic amine scaffoldsRéjean Ruel, Alexandre L'Heureux, Carl Thibeault, et al.
Bioorganic & Medicinal Chemistry Letters|September 11, 2016
Synthesis and P1' SAR exploration of potent macrocyclic tissue factor-factor VIIa inhibitorsVladimir Uladzimir Ladziata, Peter W Glunz, Yan Zou, et al.
Bioorganic & Medicinal Chemistry Letters|May 16, 2007
Design and synthesis of benzoazepinone-derived cyclic malonamides and aminoamides as potent gamma-secretase inhibitorsMichael G Yang, Jian-Liang Shi, Dilip P Modi, et al.
Pageof 42