Search Count: 24
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Structure Of Glutamate Dehydrogenase Complexed With Bithionol
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2009-06-09 Classification: OXIDOREDUCTASE Ligands: GLU, NDP, GTP, B1T |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2009-06-09
Ligands: GLU, NDP, GTP, B1T
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Crystal Structure Of Bovine Glutamate Dehydrogenase Complexed With Hexachlorophene
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:3.00 Å Release Date: 2009-06-09 Classification: OXIDOREDUCTASE Ligands: GLU, NDP, GTP, H3P |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2009-06-09
Ligands: GLU, NDP, GTP, H3P
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Glutamate Dehydrogenase Complexed With Gw5074
Organism: Bos taurus
Method: X-RAY DIFFRACTION Resolution:2.50 Å Release Date: 2009-06-09 Classification: OXIDOREDUCTASE Ligands: GLU, NDP, GTP, GWD |
Organism: Bos taurus
Method: X-RAY DIFFRACTION
Release Date: 2009-06-09
Ligands: GLU, NDP, GTP, GWD
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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
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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: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
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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: LZ5 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ5
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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:2.25 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZM |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZM
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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:2.20 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ7 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ7
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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:2.19 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ8 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ8
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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:2.15 Å Release Date: 2008-08-05 Classification: TRANSFERASE Ligands: LZ9 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2008-08-05
Ligands: LZ9
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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: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
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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: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
 |
Fragment Based P38 Inhibitors
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2005-11-03 Classification: TRANSFERASE Ligands: L09 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2005-11-03
Ligands: L09
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Identification Of Novel P38 Alpha Map Kinase Inhibitors Using Fragment-Based Lead Generation.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2005-11-03 Classification: TRANSFERASE Ligands: LI2, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2005-11-03
Ligands: LI2, GOL
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Identification Of Novel P38 Alpha Map Kinase Inhibitors Using Fragment-Based Lead Generation.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2005-11-03 Classification: TRANSFERASE Ligands: WBT |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2005-11-03
Ligands: WBT