Index | Ligand Name | Structure | PDB code | ligand desolvation |
1 | 1hk | Crystal Structure of the CHK1 | 4ftm | 91.78 |
2 | 1ao | X-RAY Crystal structure of compound 40 bound to human chk1 kinase domain | 4hyi | 91.6 |
3 | 09h | X-ray crystal structure of compound 1 bound to human CHK1 kinase domain | 3u9n | 90.28 |
4 | 12c | 4-(Aminoalkylamino)-3-Benzimidazole-Quinolinones As Potent CHK1 Inhibitors | 2gdo | 89.51 |
5 | 77a | Structure of h-CHK1 complexed with A771129 | 2e9p | 88.19 |
6 | a25 | Structure of h-CHK1 complexed with A780125 | 2e9u | 87.91 |
7 | zyr | Crystal structure of checkpoint kinase 1 (Chk1) in complex with inhibitors | 2wmr | 86.74 |
8 | 1am | X-RAY Crystal structure of compound 39 bound to human chk1 kinase domain | 4hyh | 86.65 |
9 | 3d3 | Identification of chemically diverse Chk1 inhibitors by receptor- based virtual screening | 2cgx | 86.37 |
10 | 4ym | Crystal structure of checkpoint kinase 1 (Chk1) in complex with inhibitors | 2ym4 | 85.81 |
11 | 22k | X-ray crystal structure of compound 22k bound to human Chk1 kinase domain | 3ot3 | 85.1 |
12 | 7cs | crystal structure of Chek1 in complex with inhibitor 2a | 2qhm | 85.08 |
13 | h2k | Crystal Structure of the CHK1 | 4ft5 | 85.01 |
14 | ym8 | Crystal structure of checkpoint kinase 1 (Chk1) in complex with inhibitors | 2ym8 | 84.59 |
15 | h0k | Crystal Structure of the CHK1 | 4ftl | 84.51 |
16 | 3dv | CHK1 kinase domain in complex with aminopyrazine compound 13 | 4qyf | 84.49 |
17 | 3dl | CHK1 kinase domain in complex with diarylpyrazine compound 1 | 4qye | 84.44 |
18 | ym6 | Crystal structure of checkpoint kinase 1 (Chk1) in complex with inhibitors | 2ym6 | 83.65 |
19 | mi5 | X-ray crystal structure of compound 17r bound to human Chk1 kinase domain | 3ot8 | 82.71 |
20 | zyv | Crystal structure of checkpoint kinase 1 (Chk1) in complex with inhibitors | 2wmv | 82.67 |
21 | ydk | Discovery of Checkpoint Kinase Inhibitor AZD7762 by Structure Based Design and Optimization of Thiophene Carboxamide Ureas | 2ydk | 82.54 |
22 | hk7 | Crystal Structure of the CHK1 | 4fsy | 82.53 |
23 | x8i | Discovery of a Novel Class of triazolones as Checkpoint Kinase Inhibitors - Hit to Lead Exploration | 2x8i | 82.36 |
24 | h1k | Crystal Structure of the CHK1 | 4ft3 | 82.29 |
25 | m54 | Crystal Structure of Chek1 in Complex with Inhibitor 54 | 2r0u | 82.1 |
26 | d58 | CHK1 KINASE IN COMPLEX WITH COMPOUND 44 | 6fcf | 81.86 |
27 | df2 | Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity | 2bro | 81.71 |
28 | df1 | Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity | 2brn | 81.6 |
29 | d4z | CHK1 KINASE IN COMPLEX WITH COMPOUND 13 | 6fck | 81.31 |
30 | ym5 | Crystal structure of checkpoint kinase 1 (Chk1) in complex with inhibitors | 2ym5 | 81.06 |
31 | hk1 | Crystal Structure of the CHK1 | 4fsm | 80.85 |
32 | zyq | Crystal structure of checkpoint kinase 1 (Chk1) in complex with inhibitors | 2wmq | 80.83 |
33 | d4q | CHK1 KINASE IN COMPLEX WITH COMPOUND 13 | 6fc8 | 80.73 |
34 | hk9 | Crystal Structure of the CHK1 | 4ft0 | 80.07 |
35 | 7hk | Crystal Structure of the CHK1 | 4ftu | 79.98 |
36 | c73 | X-ray crystal structure of compound 1 bound to human CHK1 kinase domain | 3pa5 | 79.39 |
37 | hk5 | Crystal Structure of the CHK1 | 4fsu | 79.05 |
38 | pfq | Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity | 2brb | 78.9 |
39 | ydj | Discovery of Checkpoint Kinase Inhibitor AZD7762 by Structure Based Design and Optimization of Thiophene Carboxamide Ureas | 2ydj | 78.68 |
40 | x8e | Discovery of a Novel Class of triazolones as Checkpoint Kinase Inhibitors - Hit to Lead Exploration | 2x8e | 78.18 |
41 | c70 | X-ray crystal structure of compound 70 bound to human CHK1 kinase domain | 3pa3 | 78 |
42 | 1ko | X-RAY Crystal structure of compound 22a (R)-2-(4-chlorophenyl)-8-(piperidin-3-ylamino)imidazo[1,2-c]pyrimidine-5-carboxamide bound to human chk1 kinase domain | 4jik | 77.64 |
43 | 2hk | Crystal Structure of the CHK1 | 4ftn | 77.6 |
44 | dfy | Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity | 2brg | 77.59 |
45 | zyw | Crystal structure of checkpoint kinase 1 (Chk1) in complex with inhibitors | 2wmw | 77.51 |
46 | c72 | X-ray crystal structure of compound 2a bound to human CHK1 kinase domain | 3pa4 | 77.2 |
47 | s25 | Crystal structure of Chk1 in complex with inhibitor S25 | 3tki | 76.96 |
48 | 5be | Novel kinase profile highlights the temporal basis of context dependent checkpoint pathways to cell death | 3nlb | 75.71 |
49 | hk6 | Crystal Structure of the CHK1 | 4fsw | 75.55 |
50 | dfw | Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity | 2brh | 75.03 |
51 | zy6 | Crystal structure of checkpoint kinase 1 (Chk1) in complex with inhibitors | 2wmx | 74.83 |
52 | ym3 | Crystal structure of checkpoint kinase 1 (Chk1) in complex with inhibitors | 2ym3 | 74.44 |
53 | 710 | crystal structure of Chek1 in complex with inhibitor 20 | 2hog | 74.31 |
54 | 4hk | Crystal Structure of the CHK1 | 4ftq | 73.89 |
55 | 3x7 | CHK1 kinase domain with diazacarbazole compound 19 | 4rvm | 73.87 |
56 | 85a | Structure of h-CHK1 complexed with A859017 | 2e9v | 73.48 |
57 | 6hk | Crystal Structure of the CHK1 | 4ftt | 72.64 |
58 | hk8 | Crystal Structure of the CHK1 | 4fsz | 72.46 |
59 | a58 | Crystal Structure of the CHK1 | 4fsn | 72.39 |
60 | a58 | Structure of h-CHK1 complexed with AA582939 | 2e9o | 71.34 |
61 | pfp | Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity | 2br1 | 71.25 |
62 | 199 | Co-crystal structure of Checkpoint Kinase Chk1 with a pyrrolo-pyridine inhibitor | 1zys | 70.84 |
63 | 306 | crystal structure of chek1 in complex with inhibitor 22 | 2hy0 | 70.81 |
64 | 5cv | Identification of Novel, in vivo Active Chk1 Inhibitors Utilizing Structure Guided Drug Design | 5dls | 70.15 |
65 | 3dw | CHK1 kinase domain in complex with diazacarbazole compound 14 | 4qyg | 69.71 |
66 | hk0 | Crystal Structure of the CHK1 | 4gh2 | 68.73 |
67 | 76a | Structure of h-CHK1 complexed with A767085 | 2e9n | 68.46 |
68 | 422 | crystal structure of Chek1 in complex with inhibitor 1 | 2hxl | 66.68 |
69 | h8k | Crystal Structure of the CHK1 | 4ftj | 66.3 |
70 | h7k | Crystal Structure of the CHK1 | 4fti | 65.83 |
71 | 3hk | Crystal Structure of the CHK1 | 4fto | 65.64 |
72 | 373 | crystal structure of Chek1 in complex with inhibitor 2 | 2hxq | 65.29 |
73 | agx | Characterization of the Chk1 allosteric inhibitor binding site | 3jvr | 64.46 |
74 | 38m | Crystal structure of chk1 kinase in complex with inhibitor 38 | 3f9n | 62.95 |
75 | ydi | Discovery of Checkpoint Kinase Inhibitor AZD7762 by Structure Based Design and Optimization of Thiophene Carboxamide Ureas | 2ydi | 62.07 |
76 | 07s | Crystal structure of Chk1 in complex with inhibitor S01 | 3tkh | 55.89 |