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Article title matches

  1. Category:Anti-sulfonamides antibody (57 bytes)
    1: List of pages with the keyword Anti-sulfonamides antibody

Page text matches

  1. 2j94 (5,654 bytes)
    26: ...-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl }sulfonamides with different P1 groups are described. These dat...
    28: ...-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl }sulfonamides.,Chan C, Borthwick AD, Brown D, Burns-Kurtis CL, ...
  2. 2j95 (5,600 bytes)
    26: ...-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl }sulfonamides with different P1 groups are described. These dat...
    28: ...-morpholin-4-yl-2-oxoethyl]-2-oxopyrrolidin-3-yl }sulfonamides.,Chan C, Borthwick AD, Brown D, Burns-Kurtis CL, ...
  3. 2bmb (5,025 bytes)
    24: ...ctious diseases, and its activity is inhibited by sulfonamides and sulfones. These drugs are typically used as p...
  4. 2c4v (3,886 bytes)
    24: ...HQase/AH9095 complex crystal structure shows that sulfonamides can form a scaffold for nonsubstrate-like inhibit...
  5. 2c4w (4,037 bytes)
    24: ...HQase/AH9095 complex crystal structure shows that sulfonamides can form a scaffold for nonsubstrate-like inhibit...
  6. 2c57 (3,903 bytes)
    24: ...HQase/AH9095 complex crystal structure shows that sulfonamides can form a scaffold for nonsubstrate-like inhibit...
  7. 2q3k (10,729 bytes)
    24: ...tease. Recently a new class of inhibitors, lysine sulfonamides, was developed to combat the resistant variants o...
  8. 1bn1 (5,634 bytes)
    26: ... at the C-4 position of bicyclic thienothiazene-6-sulfonamides; the C-4 substituent can interact with His64, the...
  9. 1bn4 (5,625 bytes)
    26: ... at the C-4 position of bicyclic thienothiazene-6-sulfonamides; the C-4 substituent can interact with His64, the...
  10. 4hjs (7,724 bytes)
    16: ...fluorogenic stilbene-based vinyl amides and vinyl sulfonamides that covalently modify transthyretin (TTR) tracel...
    18: Stilbene vinyl sulfonamides as fluorogenic sensors of and traceless covalent ...
  11. 1gfw (5,554 bytes)
    24: ...rted peptide-based caspase inhibitors, the isatin sulfonamides derive their selectivity for caspases 3 and 7 by ...
  12. 1yw7 (4,852 bytes)
    24: ...nhibitors of MetAP2, a series of anthranilic acid sulfonamides with micromolar affinities for human MetAP2 were ...
    26: Discovery and optimization of anthranilic acid sulfonamides as inhibitors of methionine aminopeptidase-2: a s...
  13. 1yw8 (4,113 bytes)
    22: ...nhibitors of MetAP2, a series of anthranilic acid sulfonamides with micromolar affinities for human MetAP2 were ...
    24: Discovery and optimization of anthranilic acid sulfonamides as inhibitors of methionine aminopeptidase-2: a s...
  14. 1yw9 (4,927 bytes)
    24: ...nhibitors of MetAP2, a series of anthranilic acid sulfonamides with micromolar affinities for human MetAP2 were ...
    26: Discovery and optimization of anthranilic acid sulfonamides as inhibitors of methionine aminopeptidase-2: a s...
  15. 2g8n (5,171 bytes)
    24: ...or much of the enhanced inhibitory potency of the sulfonamides versus the sulfones.
    26: ...,3,4-tetrahydroisoquinolines with their isosteric sulfonamides to the active site of phenylethanolamine N-methyl...
  16. 2ga2 (4,397 bytes)
    24: ...ve site metal. After a series of anthranilic acid sulfonamides with micromolar affinities was identified, chemis...
  17. 2hd6 (5,747 bytes)
    26: ...geting the tumor-associated isoforms is reported. Sulfonamides incorporating 3,3'-dithiodipropionamide/2,2'-dith...
    28: ...arbonic anhydrase inhibitors: Hypoxia-activatable sulfonamides incorporating disulfide bonds that target the tum...
  18. 8q19 (3,709 bytes)
    14: ...e binding modes that exhibit both similarities to sulfonamides and distinct orientations of the ligand tail. Our...
  19. 8q1a (3,703 bytes)
    14: ...e binding modes that exhibit both similarities to sulfonamides and distinct orientations of the ligand tail. Our...
  20. 8q18 (3,714 bytes)
    14: ...e binding modes that exhibit both similarities to sulfonamides and distinct orientations of the ligand tail. Our...

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