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Daniel L Cheney

Showing results (31-40 of 46) with videos related to

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Bioorganic & Medicinal Chemistry Letters|December 19, 2006
Pyrazole-based factor Xa inhibitors containing N-arylpiperidinyl P4 residuesJennifer X Qiao, Xuhong Cheng, Joanne M Smallheer, et al.
Bioorganic & Medicinal Chemistry Letters|March 27, 2003
Identification of novel and potent isoquinoline aminooxazole-based IMPDH inhibitorsPing Chen, Derek Norris, Kristin D Haslow, et al.
Journal of Medicinal Chemistry|March 13, 2015
Discovery of novel P1 groups for coagulation factor VIIa inhibition using fragment-based screeningDaniel L Cheney, Jeffrey M Bozarth, William J Metzler, et al.
ACS Medicinal Chemistry Letters|December 21, 2016
Discovery of Phenylglycine Lactams as Potent Neutral Factor VIIa InhibitorsNicholas R Wurtz, Brandon L Parkhurst, Wen Jiang, et al.
Bioorganic & Medicinal Chemistry Letters|May 3, 2017
Neutral macrocyclic factor VIIa inhibitorsNicholas R Wurtz, Brandon L Parkhurst, Indawati DeLucca, et al.
Bioorganic & Medicinal Chemistry Letters|July 13, 2013
Nonbenzamidine acylsulfonamide tissue factor-factor VIIa inhibitorsPeter W Glunz, Xiaojun Zhang, Yan Zou, et al.
ACS Medicinal Chemistry Letters|June 16, 2022
Discovery of Heteroaryl Urea Isosteres for Formyl Peptide Receptor 2 AgonistsNicholas R Wurtz, James A Johnson, Andrew Viet, et al.
Journal of Medicinal Chemistry|July 26, 2016
Discovery of a Highly Potent, Selective, and Orally Bioavailable Macrocyclic Inhibitor of Blood Coagulation Factor VIIa-Tissue Factor ComplexXiaojun Zhang, Peter W Glunz, James A Johnson, et al.
Bioorganic & Medicinal Chemistry Letters|February 3, 2005
De novo design, synthesis, and in vitro activity of LFA-1 antagonists based on a bicyclic[5.5]hydantoin scaffoldDominique Potin, Michele Launay, Eric Nicolai, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Design and Synthesis of Phenylpyrrolidine Phenylglycinamides As Highly Potent and Selective TF-FVIIa InhibitorsXiaojun Zhang, Wen Jiang, Swanee Jacutin-Porte, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Bioorganic & Medicinal Chemistry Letters|December 19, 2006
Pyrazole-based factor Xa inhibitors containing N-arylpiperidinyl P4 residuesJennifer X Qiao, Xuhong Cheng, Joanne M Smallheer, et al.
Bioorganic & Medicinal Chemistry Letters|March 27, 2003
Identification of novel and potent isoquinoline aminooxazole-based IMPDH inhibitorsPing Chen, Derek Norris, Kristin D Haslow, et al.
Journal of Medicinal Chemistry|March 13, 2015
Discovery of novel P1 groups for coagulation factor VIIa inhibition using fragment-based screeningDaniel L Cheney, Jeffrey M Bozarth, William J Metzler, et al.
ACS Medicinal Chemistry Letters|December 21, 2016
Discovery of Phenylglycine Lactams as Potent Neutral Factor VIIa InhibitorsNicholas R Wurtz, Brandon L Parkhurst, Wen Jiang, et al.
Bioorganic & Medicinal Chemistry Letters|May 3, 2017
Neutral macrocyclic factor VIIa inhibitorsNicholas R Wurtz, Brandon L Parkhurst, Indawati DeLucca, et al.
Bioorganic & Medicinal Chemistry Letters|July 13, 2013
Nonbenzamidine acylsulfonamide tissue factor-factor VIIa inhibitorsPeter W Glunz, Xiaojun Zhang, Yan Zou, et al.
ACS Medicinal Chemistry Letters|June 16, 2022
Discovery of Heteroaryl Urea Isosteres for Formyl Peptide Receptor 2 AgonistsNicholas R Wurtz, James A Johnson, Andrew Viet, et al.
Journal of Medicinal Chemistry|July 26, 2016
Discovery of a Highly Potent, Selective, and Orally Bioavailable Macrocyclic Inhibitor of Blood Coagulation Factor VIIa-Tissue Factor ComplexXiaojun Zhang, Peter W Glunz, James A Johnson, et al.
Bioorganic & Medicinal Chemistry Letters|February 3, 2005
De novo design, synthesis, and in vitro activity of LFA-1 antagonists based on a bicyclic[5.5]hydantoin scaffoldDominique Potin, Michele Launay, Eric Nicolai, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Design and Synthesis of Phenylpyrrolidine Phenylglycinamides As Highly Potent and Selective TF-FVIIa InhibitorsXiaojun Zhang, Wen Jiang, Swanee Jacutin-Porte, et al.
Pageof 5