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Organic & Biomolecular Chemistry
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June 16, 2007
Structure-based design of 2-arylamino-4-cyclohexylmethoxy-5-nitroso-6-aminopyrimidine inhibitors of cyclin-dependent kinase 2
Francesco Marchetti, Kerry L Sayle, Johanne Bentley, et al.
ACS Combinatorial Science
|
July 12, 2016
High-Throughput Screening and Hit Validation of Extracellular-Related Kinase 5 (ERK5) Inhibitors
Stephanie M Myers, Ruth H Bawn, Louise C Bisset, et al.
Journal of Medicinal Chemistry
|
October 13, 2006
Small-molecule inhibitors of the MDM2-p53 protein-protein interaction based on an isoindolinone scaffold
Ian R Hardcastle, Shafiq U Ahmed, Helen Atkins, et al.
Journal of Medicinal Chemistry
|
November 18, 2010
DNA-dependent protein kinase (DNA-PK) inhibitors. Synthesis and biological activity of quinolin-4-one and pyridopyrimidin-4-one surrogates for the chromen-4-one chemotype
Céline Cano, Olivier R Barbeau, Christine Bailey, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 28, 2003
Structure-based design of 2-arylamino-4-cyclohexylmethyl-5-nitroso-6-aminopyrimidine inhibitors of cyclin-dependent kinases 1 and 2
Kerry L Sayle, Johanne Bentley, F Thomas Boyle, et al.
Journal of Medicinal Chemistry
|
July 26, 2002
Probing the ATP ribose-binding domain of cyclin-dependent kinases 1 and 2 with O(6)-substituted guanine derivatives
Ashleigh E Gibson, Christine E Arris, Johanne Bentley, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 17, 2002
4-Alkoxy-2,6-diaminopyrimidine derivatives: inhibitors of cyclin dependent kinases 1 and 2
Veronique Mesguiche, Rachel J Parsons, Christine E Arris, et al.
Journal of Medicinal Chemistry
|
August 24, 2000
Identification of novel purine and pyrimidine cyclin-dependent kinase inhibitors with distinct molecular interactions and tumor cell growth inhibition profiles
C E Arris, F T Boyle, A H Calvert, et al.
Journal of Medicinal Chemistry
|
July 9, 2004
N2-substituted O6-cyclohexylmethylguanine derivatives: potent inhibitors of cyclin-dependent kinases 1 and 2
Ian R Hardcastle, Christine E Arris, Johanne Bentley, et al.
Nature Structural Biology
|
September 24, 2002
Structure-based design of a potent purine-based cyclin-dependent kinase inhibitor
Thomas G Davies, Johanne Bentley, Christine E Arris, et al.
Page
of 20
Search research articles
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Showing results (171-180 of 192) with videos related to
Sort By:
Page
of 20
Organic & Biomolecular Chemistry
|
June 16, 2007
Structure-based design of 2-arylamino-4-cyclohexylmethoxy-5-nitroso-6-aminopyrimidine inhibitors of cyclin-dependent kinase 2
Francesco Marchetti, Kerry L Sayle, Johanne Bentley, et al.
ACS Combinatorial Science
|
July 12, 2016
High-Throughput Screening and Hit Validation of Extracellular-Related Kinase 5 (ERK5) Inhibitors
Stephanie M Myers, Ruth H Bawn, Louise C Bisset, et al.
Journal of Medicinal Chemistry
|
October 13, 2006
Small-molecule inhibitors of the MDM2-p53 protein-protein interaction based on an isoindolinone scaffold
Ian R Hardcastle, Shafiq U Ahmed, Helen Atkins, et al.
Journal of Medicinal Chemistry
|
November 18, 2010
DNA-dependent protein kinase (DNA-PK) inhibitors. Synthesis and biological activity of quinolin-4-one and pyridopyrimidin-4-one surrogates for the chromen-4-one chemotype
Céline Cano, Olivier R Barbeau, Christine Bailey, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 28, 2003
Structure-based design of 2-arylamino-4-cyclohexylmethyl-5-nitroso-6-aminopyrimidine inhibitors of cyclin-dependent kinases 1 and 2
Kerry L Sayle, Johanne Bentley, F Thomas Boyle, et al.
Journal of Medicinal Chemistry
|
July 26, 2002
Probing the ATP ribose-binding domain of cyclin-dependent kinases 1 and 2 with O(6)-substituted guanine derivatives
Ashleigh E Gibson, Christine E Arris, Johanne Bentley, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 17, 2002
4-Alkoxy-2,6-diaminopyrimidine derivatives: inhibitors of cyclin dependent kinases 1 and 2
Veronique Mesguiche, Rachel J Parsons, Christine E Arris, et al.
Journal of Medicinal Chemistry
|
August 24, 2000
Identification of novel purine and pyrimidine cyclin-dependent kinase inhibitors with distinct molecular interactions and tumor cell growth inhibition profiles
C E Arris, F T Boyle, A H Calvert, et al.
Journal of Medicinal Chemistry
|
July 9, 2004
N2-substituted O6-cyclohexylmethylguanine derivatives: potent inhibitors of cyclin-dependent kinases 1 and 2
Ian R Hardcastle, Christine E Arris, Johanne Bentley, et al.
Nature Structural Biology
|
September 24, 2002
Structure-based design of a potent purine-based cyclin-dependent kinase inhibitor
Thomas G Davies, Johanne Bentley, Christine E Arris, et al.
Page
of 20