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Crystal structure of HCV NS3 protease with a boronate inhibitorCrystal structure of HCV NS3 protease with a boronate inhibitor
Structural highlights
FunctionPublication Abstract from PubMedWe have designed and synthesized a novel series of alpha-amino cyclic boronates and incorporated them successfully in several acyclic templates at the P1 position. These compounds are inhibitors of the HCV NS3 serine protease, and structural studies show that they inhibit the NS3 protease by trapping the Ser-139 hydroxyl group in the active site. Synthetic methodologies and SARs of this series of compounds are described. Synthesis and evaluation of novel alpha-amino cyclic boronates as inhibitors of HCV NS3 protease.,Li X, Zhang YK, Liu Y, Ding CZ, Li Q, Zhou Y, Plattner JJ, Baker SJ, Qian X, Fan D, Liao L, Ni ZJ, White GV, Mordaunt JE, Lazarides LX, Slater MJ, Jarvest RL, Thommes P, Ellis M, Edge CM, Hubbard JA, Somers D, Rowland P, Nassau P, McDowell B, Skarzynski TJ, Kazmierski WM, Grimes RM, Wright LL, Smith GK, Zou W, Wright J, Pennicott LE Bioorg Med Chem Lett. 2010 Jun 15;20(12):3550-6. Epub 2010 May 20. PMID:20493689[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See AlsoReferences
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Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)
OCA- Hepacivirus C
- Large Structures
- Baker SJ
- Ding CZ
- Edge CM
- Ellis M
- Fan D
- Grimes RM
- Hubbard JA
- Jarvest RL
- Kazmierski WM
- Lazarides LX
- Li Q
- Li X
- Liao L
- Liu Y
- McDowell B
- Mordaunt JE
- Nassau P
- Ni Z-J
- Pennicott LE
- Plattner JJ
- Qian X
- Rowland P
- Skarzynski TJ
- Slater MJ
- Smith GK
- Somers DO
- Thommes P
- White GV
- Wright J
- Wright LL
- Zhang Y-K
- Zhou Y
- Zou W