Zobrazeno 1 - 10
of 2 349
pro vyhledávání: '"Jonathan Coates"'
Publikováno v:
Clinical Psychology Forum. 1:72-81
Publikováno v:
Proceedings of the 41st ACM SIGPLAN Conference on Programming Language Design and Implementation
Emrich, F, Lindley, S, Stolarek, J, Cheney, J & Coates, J 2020, FreezeML : Complete and Easy Type Inference for First-Class Polymorphism . in Proceedings of the 41st ACM SIGPLAN Conference on Programming Language Design and Implementation . Association for Computing Machinery (ACM), pp. 423-437, 41st ACM SIGPLAN Conference on Programming Language Design and Implementation, London, United Kingdom, 15/06/20 . https://doi.org/10.1145/3385412.3386003
PLDI
Emrich, F, Lindley, S, Stolarek, J, Cheney, J & Coates, J 2020, FreezeML : Complete and Easy Type Inference for First-Class Polymorphism . in Proceedings of the 41st ACM SIGPLAN Conference on Programming Language Design and Implementation . Association for Computing Machinery (ACM), pp. 423-437, 41st ACM SIGPLAN Conference on Programming Language Design and Implementation, London, United Kingdom, 15/06/20 . https://doi.org/10.1145/3385412.3386003
PLDI
ML is remarkable in providing statically typed polymorphism without the programmer ever having to write any type annotations. The cost of this parsimony is that the programmer is limited to a form of polymorphism in which quantifiers can occur only a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bea7287ff18673400fc09a6d9808581
Autor:
Renate Griffith, Neal Dalton, Stephen G. Pyne, John B. Bremner, Nicholas Vandegraaff, Christopher P. Gordon, David Ian Rhodes, John Deadman, Paul A. Keller, Jonathan Coates
Publikováno v:
Tetrahedron. 74:1253-1268
As of mid-2017, only one structure of the human immunodeficiency virus (HIV) integrase core domain co-crystallised with an active site inhibitor was reported. In this structure (1QS4), integrase is complexed with a diketo-acid based strand-transfer i
Publikováno v:
Pain Management. 7:223-227
Autor:
Christopher P. Gordon, Timothy P. Boyle, Stephen G. Pyne, Nicholas Vandegraaf, Neal Dalton, David Ian Rhodes, John B. Bremner, John Deadman, Paul A. Keller, Jonathan Coates
Publikováno v:
Organic & Biomolecular Chemistry. 14:6010-6023
From library screening of synthetic antimicrobial peptides, an O-allyltyrosine-based tripeptide was identified to possess inhibitory activity against HIV-1 integrase (IN) exhibiting an IC50 value of 17.5 μM in a combination 3'-processing and strand
Autor:
Philip Rea, Nicholas J. Ede, John Deadman, Thomas S. Peat, Jonathan Coates, Janet Newman, Dharshini Jeevarajah, David Ian Rhodes, Nick Vandegraaff, John Martyn
Publikováno v:
ChemBioChem. 12:2311-2315
An optimised method of solution cyclisation gave us access to a series of peptides including SLKIDNLD (2). We investigated the crystallographic complexes of the HIV integrase (HIV-IN) catalytic core domain with 13 of the peptides and identified multi
Autor:
John Deadman, G. Paul Savage, Craig L. Francis, John H. Ryan, Thomas S. Peat, Jessica A. Smith, Dharshini Jeevarajah, Jonathan Coates, Janet Newman, Lisa Jane Winfield, Del Lucent, Giang Thanh Le, Neeranat Thienthong, Eric Dale Jones, David Ian Rhodes, Nick Vandegraaff
Publikováno v:
Antiviral Chemistry and Chemotherapy. 21:155-168
Background: HIV-1 integrase is a clinically validated therapeutic target for the treatment of HIV-1 infection, with one approved therapeutic currently on the market. This enzyme represents an attractive target for the development of new inhibitors to
Autor:
Xiao Feng, Changjiang Yu, Katherine Macfarlane, Giang Thanh Le, Eric Dale Jones, John Deadman, David Ian Rhodes, Neeranat Thienthong, Nick Vandegraaff, Long Lu, Xinming Li, Lisa Jane Winfield, Jonathan Coates, Neil Choi, William Issa
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:5913-5917
HIV integrase inhibitors based on a novel bicyclic pyrimidinone core is presented. Nine variations of the core scaffold are evaluated leading to optimization of the 6:6 core giving compound 48 with an EC50 of 3 nM against wild type HIV infected T-cel
Design of a series of bicyclic HIV-1 integrase inhibitors. Part 2: Azoles: Effective metal chelators
Autor:
John Deadman, Eric Dale Jones, David Ian Rhodes, Changjiang Yu, Nick Vandegraaff, Jonathan Coates, Xinming Li, Xiao Feng, Giang Thanh Le, Lisa Jane Winfield, Long Lu, Neeranat Thienthong
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:5909-5912
Synthesis of a diverse set of azoles and their utilizations as an amide isostere in the design of HIV integrase inhibitors is described. The Letter identified thiazole, oxazole, and imidazole as the most promising heterocycles. Initial SAR studies in
Autor:
John Deadman, Xiao Feng, Changjiang Yu, Jonathan Coates, Xinming Li, Eric Dale Jones, David Ian Rhodes, Nick Vandegraaff, Long Lu, Giang Thanh Le
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 20:5013-5018
A series of novel HIV integrase inhibitors active against rategravir resistant strains are reported. Initial SAR studies revealed that activities against wild-type virus were successfully maintained at single digit nanomolar level with a wide range o