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Journal of Medicinal Chemistry
|
May 2, 2015
Correction to Structure-Guided Design of a Series of MCL-1 Inhibitors with High Affinity and Selectivity
Milan Bruncko, Le Wang, George S Sheppard, et al.
Journal of Medicinal Chemistry
|
February 14, 2015
Structure-guided design of a series of MCL-1 inhibitors with high affinity and selectivity
Milan Bruncko, Le Wang, George S Sheppard, et al.
Molecular Cancer Therapeutics
|
March 20, 2024
Inhibition of MALT1 and BCL2 Induces Synergistic Antitumor Activity in Models of B-Cell Lymphoma
Joshua P Plotnik, Adam E Richardson, Haopeng Yang, et al.
Communications Medicine
|
October 25, 2023
Selective MCL-1 inhibitor ABBV-467 is efficacious in tumor models but is associated with cardiac troponin increases in patients
Junichiro Yuda, Christine Will, Darren C Phillips, et al.
Nature Cancer
|
March 8, 2022
An anti-PD-1-GITR-L bispecific agonist induces GITR clustering-mediated T cell activation for cancer immunotherapy
Sarah Chan, Nicole Belmar, Sun Ho, et al.
Molecular Cancer Therapeutics
|
March 31, 2021
Expanding the Repertoire for "Large Small Molecules": Prodrug ABBV-167 Efficiently Converts to Venetoclax with Reduced Food Effect in Healthy Volunteers
Ahmed Hamed Salem, Zhi-Fu Tao, Orlando F Bueno, et al.
ACS Medicinal Chemistry Letters
|
October 16, 2020
Discovery of A-1331852, a First-in-Class, Potent, and Orally-Bioavailable BCL-X<sub>L</sub> Inhibitor
Le Wang, George A Doherty, Andrew S Judd, et al.
Journal of Medicinal Chemistry
|
November 3, 2018
Identification of Selective Dual ROCK1 and ROCK2 Inhibitors Using Structure-Based Drug Design
Adrian D Hobson, Russell A Judge, Ana L Aguirre, et al.
ACS Medicinal Chemistry Letters
|
October 15, 2014
Discovery of a Potent and Selective BCL-XL Inhibitor with in Vivo Activity
Zhi-Fu Tao, Lisa Hasvold, Le Wang, et al.
Science Advances
|
October 4, 2024
BCL-X<sub>L</sub>-targeting antibody-drug conjugates are active in preclinical models and mitigate on-mechanism toxicity of small-molecule inhibitors
Andrew S Judd, Bhupinder Bawa, Wayne R Buck, et al.
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Showing results (221-230 of 230) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 230 results.
Journal of Medicinal Chemistry
|
May 2, 2015
Correction to Structure-Guided Design of a Series of MCL-1 Inhibitors with High Affinity and Selectivity
Milan Bruncko, Le Wang, George S Sheppard, et al.
Journal of Medicinal Chemistry
|
February 14, 2015
Structure-guided design of a series of MCL-1 inhibitors with high affinity and selectivity
Milan Bruncko, Le Wang, George S Sheppard, et al.
Molecular Cancer Therapeutics
|
March 20, 2024
Inhibition of MALT1 and BCL2 Induces Synergistic Antitumor Activity in Models of B-Cell Lymphoma
Joshua P Plotnik, Adam E Richardson, Haopeng Yang, et al.
Communications Medicine
|
October 25, 2023
Selective MCL-1 inhibitor ABBV-467 is efficacious in tumor models but is associated with cardiac troponin increases in patients
Junichiro Yuda, Christine Will, Darren C Phillips, et al.
Nature Cancer
|
March 8, 2022
An anti-PD-1-GITR-L bispecific agonist induces GITR clustering-mediated T cell activation for cancer immunotherapy
Sarah Chan, Nicole Belmar, Sun Ho, et al.
Molecular Cancer Therapeutics
|
March 31, 2021
Expanding the Repertoire for "Large Small Molecules": Prodrug ABBV-167 Efficiently Converts to Venetoclax with Reduced Food Effect in Healthy Volunteers
Ahmed Hamed Salem, Zhi-Fu Tao, Orlando F Bueno, et al.
ACS Medicinal Chemistry Letters
|
October 16, 2020
Discovery of A-1331852, a First-in-Class, Potent, and Orally-Bioavailable BCL-X<sub>L</sub> Inhibitor
Le Wang, George A Doherty, Andrew S Judd, et al.
Journal of Medicinal Chemistry
|
November 3, 2018
Identification of Selective Dual ROCK1 and ROCK2 Inhibitors Using Structure-Based Drug Design
Adrian D Hobson, Russell A Judge, Ana L Aguirre, et al.
ACS Medicinal Chemistry Letters
|
October 15, 2014
Discovery of a Potent and Selective BCL-XL Inhibitor with in Vivo Activity
Zhi-Fu Tao, Lisa Hasvold, Le Wang, et al.
Science Advances
|
October 4, 2024
BCL-X<sub>L</sub>-targeting antibody-drug conjugates are active in preclinical models and mitigate on-mechanism toxicity of small-molecule inhibitors
Andrew S Judd, Bhupinder Bawa, Wayne R Buck, et al.
Page
of 23