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- The discovery and evaluation of diaryl ether heterocyclic sulfonamides as URAT1 inhibitors for the treatment of gout. R. Ian Storer, Robert M. Owen, Andy Pike, Caroline L. Benn, Emma Armstrong, David C. Blakemore, Magda Bictash, Kathryn Costelloe, Emma Impey, Philip H. Milliken, Elisabeth Mortimer-Cassen, Hannah J. Pearce, Benjamin Pibworth, Gianna Toschi
, Med. Chem. Commun.
, 2016
, 7
, 1587
- Strengthening N⋯X halogen bonding via nitrogen substitution in the aromatic framework of halogen-substituted arylpyrazinamides. Hamid Reza Khavasi, Mahdieh Hosseini, Alireza Azhdari Tehrani, Soheila Naderi
, CrystEngComm
, 2014
, 16
, 4546
- Halogenated tennimides and trezimides: impact of halogen bonding and solvent role on porous network formation and inclusion. P. Mocilac, J. F. Gallagher
, CrystEngComm
, 2016
, 18
, 2375
- A threonine turnstile defines a dynamic amphiphilic binding motif in the AAA ATPase p97 allosteric binding site. James C. Burnett, Chaemin Lim, Brian D. Peyser, Lalith P. Samankumara, Marina Kovaliov, Raffaele Colombo, Stacie L. Bulfer, Matthew G. LaPorte, Ann R. Hermone, Connor F. McGrath, Michelle R. Arkin, Rick Gussio, Donna M. Huryn, Peter Wipf
, Org. Biomol. Chem.
, 2017
, 15
, 4096