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The Journal of Organic Chemistry
|
February 3, 2025
Factors to Consider for Synthesis in 1536-Well Plates─An Amide Coupling Case Study for PROTAC Synthesis
Rebecca Stevens, Harry E P Palmer, Afjal H Miah, et al.
Organic & Biomolecular Chemistry
|
February 12, 2014
Lead identification and structure-activity relationships of heteroarylpyrazole arylsulfonamides as allosteric CC-chemokine receptor 4 (CCR4) antagonists
Afjal H Miah, Royston C B Copley, Daniel O'Flynn, et al.
Bioorganic & Medicinal Chemistry
|
August 13, 2017
Identification of pyrazolopyrimidine arylsulfonamides as CC-chemokine receptor 4 (CCR4) antagonists
Afjal H Miah, Aurelie C Champigny, Rebecca H Graves, et al.
Chemical Society Reviews
|
April 10, 2024
Innovative, combinatorial and high-throughput approaches to degrader synthesis
Rebecca Stevens, James D F Thompson, Julie C L Fournier, et al.
RSC Medicinal Chemistry
|
December 25, 2024
Expanding the reaction toolbox for nanoscale direct-to-biology PROTAC synthesis and biological evaluation
Rebecca Stevens, Harry J Shrives, Jenni Cryan, et al.
ACS Chemical Biology
|
June 13, 2015
HaloPROTACS: Use of Small Molecule PROTACs to Induce Degradation of HaloTag Fusion Proteins
Dennis L Buckley, Kanak Raina, Nicole Darricarrere, et al.
ACS Chemical Biology
|
June 30, 2026
A Systematic Direct-to-Biology Approach Identified Potent Cereblon HaloPROTACs
Rebecca Stevens, Kwok-Ho Chan, Alice Moore, et al.
Bioorganic & Medicinal Chemistry
|
June 10, 2014
Lead identification of benzimidazolone and azabenzimidazolone arylsulfonamides as CC-chemokine receptor 4 (CCR4) antagonists
Afjal H Miah, Hossay Abas, Malcolm Begg, et al.
Journal of Medicinal Chemistry
|
November 7, 2023
Integrated Direct-to-Biology Platform for the Nanoscale Synthesis and Biological Evaluation of PROTACs
Rebecca Stevens, Enrique Bendito-Moll, David J Battersby, et al.
European Journal of Medicinal Chemistry
|
March 19, 2016
2,8-Diazaspiro[4.5]decan-8-yl)pyrimidin-4-amine potent CCR4 antagonists capable of inducing receptor endocytosis
Lena Shukla, Laura A Ajram, Malcolm Begg, et al.
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Search research articles
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Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
The Journal of Organic Chemistry
|
February 3, 2025
Factors to Consider for Synthesis in 1536-Well Plates─An Amide Coupling Case Study for PROTAC Synthesis
Rebecca Stevens, Harry E P Palmer, Afjal H Miah, et al.
Organic & Biomolecular Chemistry
|
February 12, 2014
Lead identification and structure-activity relationships of heteroarylpyrazole arylsulfonamides as allosteric CC-chemokine receptor 4 (CCR4) antagonists
Afjal H Miah, Royston C B Copley, Daniel O'Flynn, et al.
Bioorganic & Medicinal Chemistry
|
August 13, 2017
Identification of pyrazolopyrimidine arylsulfonamides as CC-chemokine receptor 4 (CCR4) antagonists
Afjal H Miah, Aurelie C Champigny, Rebecca H Graves, et al.
Chemical Society Reviews
|
April 10, 2024
Innovative, combinatorial and high-throughput approaches to degrader synthesis
Rebecca Stevens, James D F Thompson, Julie C L Fournier, et al.
RSC Medicinal Chemistry
|
December 25, 2024
Expanding the reaction toolbox for nanoscale direct-to-biology PROTAC synthesis and biological evaluation
Rebecca Stevens, Harry J Shrives, Jenni Cryan, et al.
ACS Chemical Biology
|
June 13, 2015
HaloPROTACS: Use of Small Molecule PROTACs to Induce Degradation of HaloTag Fusion Proteins
Dennis L Buckley, Kanak Raina, Nicole Darricarrere, et al.
ACS Chemical Biology
|
June 30, 2026
A Systematic Direct-to-Biology Approach Identified Potent Cereblon HaloPROTACs
Rebecca Stevens, Kwok-Ho Chan, Alice Moore, et al.
Bioorganic & Medicinal Chemistry
|
June 10, 2014
Lead identification of benzimidazolone and azabenzimidazolone arylsulfonamides as CC-chemokine receptor 4 (CCR4) antagonists
Afjal H Miah, Hossay Abas, Malcolm Begg, et al.
Journal of Medicinal Chemistry
|
November 7, 2023
Integrated Direct-to-Biology Platform for the Nanoscale Synthesis and Biological Evaluation of PROTACs
Rebecca Stevens, Enrique Bendito-Moll, David J Battersby, et al.
European Journal of Medicinal Chemistry
|
March 19, 2016
2,8-Diazaspiro[4.5]decan-8-yl)pyrimidin-4-amine potent CCR4 antagonists capable of inducing receptor endocytosis
Lena Shukla, Laura A Ajram, Malcolm Begg, et al.
Page
of 2