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Article title matches

  1. Category:Indazole inhibitor (49 bytes)
    1: List of pages with the keyword Indazole inhibitor
  2. Category:Indazole (39 bytes)
    1: List of pages with the keyword Indazole

Page text matches

  1. 3w2c (3,605 bytes)
    2: ...re of Aurora kinase A complexed to benzoimidazole-indazole inhibitor XV==
  2. 2uzw (7,305 bytes)
    2: ==PKA structures of indazole-pyridine series of AKT inhibitors==
    24: ... analogues of 7 at the C-6 position of the methyl indazole scaffold. These modifications resulted in the dis...
    26: ...ses of potent, selective, and orally bioavailable indazole-pyridine series of protein kinase b/akt inhibitor...
  3. 2uzt (7,322 bytes)
    2: ==PKA structures of AKT, indazole-pyridine inhibitors==
    24: ... analogues of 7 at the C-6 position of the methyl indazole scaffold. These modifications resulted in the dis...
    26: ...ses of potent, selective, and orally bioavailable indazole-pyridine series of protein kinase b/akt inhibitor...
  4. 2uzu (7,340 bytes)
    2: ==PKA structures of indazole-pyridine series of AKT inhibitors==
    24: ... analogues of 7 at the C-6 position of the methyl indazole scaffold. These modifications resulted in the dis...
    26: ...ses of potent, selective, and orally bioavailable indazole-pyridine series of protein kinase b/akt inhibitor...
  5. 2uzv (5,295 bytes)
    2: ==PKA structures of indazole-pyridine series of AKT inhibitors==
    24: ... analogues of 7 at the C-6 position of the methyl indazole scaffold. These modifications resulted in the dis...
    26: ...ses of potent, selective, and orally bioavailable indazole-pyridine series of protein kinase b/akt inhibitor...
  6. 2c3l (8,134 bytes)
    7: ...e name='pdbligand=IDZ:3-(1H-BENZIMIDAZOL-2-YL)-1H-INDAZOLE'>IDZ</scene>, <scene name='pdbligand=SO4:SULFATE+...
    24: ...inhibitors complexed with Chk1 show that only the indazole series utilizes the pocket of interest. Therefore...
  7. 2c3j (8,118 bytes)
    24: ...inhibitors complexed with Chk1 show that only the indazole series utilizes the pocket of interest. Therefore...
  8. 2c3k (8,104 bytes)
    24: ...inhibitors complexed with Chk1 show that only the indazole series utilizes the pocket of interest. Therefore...
  9. Dehaloperoxidase 3D structures (2,349 bytes)
    31: **[[5lk9]] - AoDHP B + indazole<br />
  10. 2hog (7,580 bytes)
    24: ...s and heteroaryl groups at the C6 position of the indazole ring system provided sufficient Chek1 potency and...
    26: 3-(Indol-2-yl)indazoles as Chek1 kinase inhibitors: Optimization of pote...
  11. 7nr4 (4,973 bytes)
    2: ==X-RAY STRUCTURE OF PRMT6 IN COMPLEX WITH indazole type inhibitor==
  12. 1dm6 (4,756 bytes)
    24: ...). A small-molecule inhibitor of NOS (3-Br-7-nitroindazole, 7-NIBr) is profoundly neuroprotective in mouse m...
    26: ...structure of nitric oxide synthase bound to nitro indazole reveals a novel inactivation mechanism.,Raman CS,...
  13. 1ed5 (4,545 bytes)
    24: ...). A small-molecule inhibitor of NOS (3-Br-7-nitroindazole, 7-NIBr) is profoundly neuroprotective in mouse m...
    26: ...structure of nitric oxide synthase bound to nitro indazole reveals a novel inactivation mechanism.,Raman CS,...
  14. 2ymd (3,770 bytes)
    14: ...erve a critical cation-pi interaction between the indazole moiety of the ligand and a cationic centre in loo...
  15. 8nse (4,509 bytes)
    24: ...). A small-molecule inhibitor of NOS (3-Br-7-nitroindazole, 7-NIBr) is profoundly neuroprotective in mouse m...
    26: ...structure of nitric oxide synthase bound to nitro indazole reveals a novel inactivation mechanism.,Raman CS,...
  16. 2oh0 (6,358 bytes)
    24: ...s have been introduced at the C-6 position of the indazole scaffold, leading to a significant drop in Akt po...
  17. 2ojf (6,366 bytes)
    24: ...s have been introduced at the C-6 position of the indazole scaffold, leading to a significant drop in Akt po...
  18. 4izy (5,712 bytes)
    14: A novel series of indole/indazole-aminopyrimidines was designed and synthesized wit...
    16: Development of indole/indazole-aminopyrimidines as inhibitors of c-Jun N-termina...
  19. 4jg7 (7,125 bytes)
    16: ...se domain. Guided by X-ray co-crystal structures, indazole fragment 1 was elaborated to afford 12 (RMM-46), ...
  20. 4jg8 (7,175 bytes)
    16: ...se domain. Guided by X-ray co-crystal structures, indazole fragment 1 was elaborated to afford 12 (RMM-46), ...

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