Search Count: 14
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Ii With 2-Chloro-4-{[(4,6-Dimethylpyrimidin-2-Yl)Sulfanyl]Acetyl}Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2013-11-06 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, DMS, MES, E1E |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-06
Ligands: ZN, DMS, MES, E1E
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Ii With 2-Chloro-4-[(Pyrimidin-2-Ylsulfanyl)Acetyl]Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.00 Å Release Date: 2013-11-06 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, E1F, DMS, MES |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-06
Ligands: ZN, E1F, DMS, MES
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Xiii With 2-Chloro-4-{[(4,6-Dimethylpyrimidin-2-Yl)Sulfanyl]Acetyl}Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2013-11-06 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, E1E, PGE |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-06
Ligands: ZN, E1E, PGE
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Xiii With 2-Chloro-4-[(Pyrimidin-2-Ylsulfanyl)Acetyl]Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.40 Å Release Date: 2013-11-06 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, E1F, CIT, EDO, ACY, PEG |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-06
Ligands: ZN, E1F, CIT, EDO, ACY, PEG
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Crystal Structure Of Catalytic Domain Of Human Carbonic Anhydrase Isozyme Xii With 2-Chloro-4-[(Pyrimidin-2-Ylsulfanyl)Acetyl]Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.45 Å Release Date: 2013-11-06 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, E1F, EDO, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-06
Ligands: ZN, E1F, EDO, SO4
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Crystal Structure Of Catalytic Domain Of Human Carbonic Anhydrase Isozyme Xii With 3-[(Pyrimidin-2-Ylsulfanyl)Acetyl]Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.80 Å Release Date: 2013-11-06 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, E1G, DMS, PEG, EDO |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2013-11-06
Ligands: ZN, E1G, DMS, PEG, EDO
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Ii With 4-{2-[N-(6-Methoxy-5-Nitropyrimidin-4-Yl)Amino]Ethyl}Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.68 Å Release Date: 2010-10-20 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, DMS, JS7 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-10-20
Ligands: ZN, DMS, JS7
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Ii With 4-[N-(6-Chloro-5-Nitropyrimidin-4-Yl)Amino]Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2010-10-20 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, J45, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-10-20
Ligands: ZN, J45, DMS
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Ii With 4-{[N-(6-Chloro-5-Formyl-2-Methylthiopyrimidin-4-Yl)Amino]Methyl}Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2010-10-20 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, DMS, JDR |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-10-20
Ligands: ZN, DMS, JDR
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Ii With 4-{[(5-Nitro-6-Oxo-1,6-Dihydro-4-Pyrimidinyl)Amino]Methyl}Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2010-10-20 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, J90, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-10-20
Ligands: ZN, J90, DMS
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Ii With 4-{[N-(6-Methoxy-5-Nitropyrimidin-4-Yl)Amino]Methyl}Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2010-10-20 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, DMS, J71 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-10-20
Ligands: ZN, DMS, J71
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Ii With 4-{[N-(6-Benzylamino-5-Nitropyrimidin-4-Yl)Amino]Methyl}Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.50 Å Release Date: 2010-10-20 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, DMS, J75 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-10-20
Ligands: ZN, DMS, J75
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Ii With 4-[N-(6-Chloro-5-Formyl-2-Methylthiopyrimidin-4-Yl)Amino]Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.15 Å Release Date: 2010-10-20 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, DMS, J43, UNL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-10-20
Ligands: ZN, DMS, J43, UNL
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Ii With 3-Methylthiobenzimidazo[1,2-C][1,2,3]Thiadiazol-7-Sulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.44 Å Release Date: 2010-03-02 Classification: LYASE Ligands: V21, NA, UNX, ZN |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2010-03-02
Ligands: V21, NA, UNX, ZN