Search Count: 28
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Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: GOL, LZ1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: GOL, LZ1
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H-Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: GOL, LZ2 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: GOL, LZ2
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ3 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ3
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: GOL, LZ4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: GOL, LZ4
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ5
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZM
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ7 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ7
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.19 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ8 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ8
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.15 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ9
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZA |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZA
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.89 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZB |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZB
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZC |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZC
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.68 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZD
 |
Identification Of N-(4-Piperidinyl)-4-(2,6-Dichlorobenzoylamino)-1H- Pyrazole-3-Carboxamide (At7519), A Novel Cyclin Dependent Kinase Inhibitor Using Fragment-Based X-Ray Crystallography And Structure Based Drug Design.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.85 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZE
 |
Thrombin Inhibitors
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:1.96 Å Release Date: 2006-07-04 Classification: HYDROLASE/HYDROLASE INHIBITOR |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2006-07-04
 |
Thrombin Inhibitors
Organism: Hirudo medicinalis, Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.17 Å Release Date: 2006-07-04 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: DMS, NA, C5M |
Organism: Hirudo medicinalis, Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2006-07-04
Ligands: DMS, NA, C5M
 |
Thrombin Inhibitors
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2006-07-04 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: DMS, NA, C3M |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2006-07-04
Ligands: DMS, NA, C3M
 |
Thrombin Inhibitors
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:2.14 Å Release Date: 2006-07-04 Classification: HYDROLASE/HYDROLASE INHIBITOR |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2006-07-04
 |
Thrombin Inhibitors
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:2.25 Å Release Date: 2006-07-04 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: DMS, NA, C1M |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2006-07-04
Ligands: DMS, NA, C1M
 |
Thrombin Inhibitors
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION Resolution:2.20 Å Release Date: 2006-07-04 Classification: HYDROLASE/HYDROLASE INHIBITOR Ligands: DMS, NA, C4M |
Organism: Homo sapiens, Hirudo medicinalis
Method: X-RAY DIFFRACTION
Release Date: 2006-07-04
Ligands: DMS, NA, C4M