Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Donald J. Cook"'
Autor:
Terry MacIntyre, Brian Aquila, Edward J. Hennessy, Naomi Laing, Vibha Oza, David Whitston, Victor Kamhi, Jamal Carlos Saeh, Lillian Castriotta, Li Sha, Troy Patterson, Christopher Huntington, Danyang Li, Haiyun Wang, Charles A. Omer, Alexander Hird, Melissa Vasbinder, Donald J. Cook, Michael T. Rooney, Galina Repik, Maureen Hattersley, Ammar Adam
Publikováno v:
Journal of Medicinal Chemistry. 56:9897-9919
A series of dimeric compounds based on the AVPI motif of Smac were designed and prepared as antagonists of the inhibitor of apoptosis proteins (IAPs). Optimization of cellular potency, physical properties, and pharmacokinetic parameters led to the id
Autor:
Carrie L. Balliet, Srinivasu Poondru, Charles A. Omer, Davies Audrey, Thomas Gero, Scott David, Donald J. Cook, Maria-Elena Theoclitou, Boris Tyurin, Michael Zinda
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 19:697-700
3-amido-4-anilinoquinolines are potent and highly selective inhibitors of CSF-1R. Their synthesis and SAR is reported, along with initial efforts to optimize the physical properties and PK through modifications at the quinoline 6- and 7-positions.
Autor:
Lisa Drew, Les A. Dakin, Boris Tyurin, Kirsten Bell, Maureen Hattersley, Scott David, Xiaolan Zheng, Cheryl Campbell, Thomas Gero, Donald J. Cook, Charles A. Omer, David J. Del Valle
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 19:701-705
The optimization of compounds from the 3-amido-4-anilinoquinolines series of CSF-1R kinase inhibitors is described. The series has excellent activity and kinase selectivity. Excellent physical properties and rodent PK profiles were achieved through t
Autor:
Charles A. Omer, Tracy L. Deegan, Minwei Ye, Les A. Dakin, Paul Lyne, Maureen Hattersley, Donald J. Cook, Xiaolan Zheng, Stephanos Ioannidis, Brian Aquila, Geraldine Bebernitz, Scott David
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 18:4794-4797
The bisamide class of kinase inhibitors was identified as being active against CSF-1R. The synthesis and SAR of pyridyl and thiazolyl bisamides are reported, along with the pharmacokinetic properties and in vivo activity of selected examples.
Publikováno v:
2013 25th International Symposium on Power Semiconductor Devices & IC's (ISPSD).
In this paper, we discuss the fundamental design tradeoff among specific on-resistance (Ron, sp), gate charge (Cgg), quasi-saturation, and reliability characteristics for an integrated high voltage LDMOS. A novel patterned gate design is proposed and
Autor:
Rick Phelps, Theodode Letavic, Natalie B. Feilchenfeld, Donald J. Cook, Michael J. Zierak, Santosh Sharma, Yun Shi
Publikováno v:
2013 25th International Symposium on Power Semiconductor Devices & IC's (ISPSD).
This paper presents complimentary 85V-rated LDMOS devices integrated in a 180nm power management technology platform. The devices are fabricated using a design technique which utilizes tapered dielectric regions in combination with patterned floating
Autor:
John J. Ellis-Monaghan, Natalie B. Feilchenfeld, James S. Dunn, Yun Shi, Rick Phelps, Ted Letavic, Donald J. Cook, Crystal M. Hedges, Santosh Sharma
Publikováno v:
2012 24th International Symposium on Power Semiconductor Devices and ICs.
A novel JFET redesign of a laterally scaled P-LDMOS device is presented. The P-LDMOS device has excellent Rsp as it is scaled from 90V to 170V operation. This P-LDMOS design is modified to produce a 100V PJFET with good turn-off characteristics and a
Autor:
Rick Phelps, Donald J. Cook, Helmut Nauschnig, Santosh Sharma, Georg Roerher, Alain Loiseau, Rainer Minixhofer, Theodore J. Letavic, Yun Shi, John-Ellis Monaghan, James S. Dunn, Natalie B. Feilchenfeld, Christopher Lamothe
Publikováno v:
2012 24th International Symposium on Power Semiconductor Devices and ICs.
This paper presents a 20V-rated planar dual gate oxide NLDMOS power device structure fabricated in a 180nm power management technology. The performance of the planar dual gate device structure is compared to a conventional STI-based device and it is
Autor:
Dominique Custeau, Srinivasu Poondru, Qing Ye, Minhui Shen, Donald J. Cook, Jay Ezhuthachan, Michael Howard Block, Lee John W, Paul Lyne, Scott David, Allan Wu, Mei Su, Lisa Drew, Timothy Pontz, Les A. Dakin, Stephanos Ioannidis, Tracy L. Deegan, Scott Cowen, Brian Aquila, Xiaolan Zheng
Publikováno v:
Bioorganicmedicinal chemistry letters. 19(3)
A series of amidoheteroaryl compounds were designed and synthesized as inhibitors of B-Raf kinase. Several compounds from the series show excellent potency in biochemical, phenotypic and mode of action cellular assays. Potent examples from the series
Autor:
Terry MacIntyre, Brian Aquila, Edward J. Hennessy, Daniel John Russell, Bin Yang, Dave Witson, Jamal Carlos Saeh, Maureen Hattersley, Paula Lewis, Michael T. Rooney, Charles A. Omer, Galina Repik, Victor Kamhi, Li Sha, Danyang Li, Haiyun Wang, John Lee, Troy Patterson, Naomi Laing, Melissa Vasbinder, Donald J. Cook, Andrew D. Ferguson, Vibha Oza, Alexander Hird
Publikováno v:
Molecular Cancer Therapeutics. 12:B100-B100
Both monomeric and dimeric SMAC (Second Mitochondria-derived Activator of Caspaces) mimetics acting as IAP (Inhibitor of apoptosis proteins) anatgonists have been reported in the clinic as well as extensively in the literature (1). The first four ami