Search Count: 30
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Crystal Structure Of A Phosphocoumarin Derivative In Complex With Human Carbonic Anhydrase Ii
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.65 Å Release Date: 2026-05-13 Classification: LYASE Ligands: ZN, A1JX9, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-05-13
Ligands: ZN, A1JX9, GOL
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Crystal Structure Of Human Carbonic Anhydrase Vii In Complex With A Benzenesulfonamide Derivative Containing The Duloxetine Moiety.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.35 Å Release Date: 2026-04-15 Classification: LYASE Ligands: ZN, A1I9B |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-04-15
Ligands: ZN, A1I9B
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Crystal Structure Of Human Carbonic Anhydrase Vii In Complex With A Benzenesufonamide Derivative Containing The Duloxetine Moiety
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2026-04-15 Classification: LYASE Ligands: ZN, A1I9C |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2026-04-15
Ligands: ZN, A1I9C
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Carbonic Anhydrase Ii In Complex With 3-Ureido Benzenesulfonamide Derivative
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.29 Å Release Date: 2022-06-08 Classification: Lyase/Inhibitor Ligands: ZN, 65M, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-06-08
Ligands: ZN, 65M, GOL
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Carbonic Anhydrase Ii In Complex With 4-Ureido Benzenesulfonamide Derivative
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.30 Å Release Date: 2022-06-08 Classification: Lyase/Inhibitor Ligands: ZN, 64W, GOL, AZI |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2022-06-08
Ligands: ZN, 64W, GOL, AZI
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Crystal Structure For The Complex Of Human Carbonic Anhydrase Ii And 3-(3-Methyl-3-Phenethylureido)Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.43 Å Release Date: 2021-11-24 Classification: LYASE Ligands: ZN, GOL, NA, RWH |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-11-24
Ligands: ZN, GOL, NA, RWH
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Human Carbonic Anhydrase Ii Bound To An Inhibitor Modified With Azidothymidine
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.34 Å Release Date: 2021-02-24 Classification: LYASE Ligands: ZN, U4V |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2021-02-24
Ligands: ZN, U4V
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Human Carbonic Anhydrase Ii In Complex With A Sulfonamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.26 Å Release Date: 2020-06-10 Classification: LYASE Ligands: ZN, L8N, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-06-10
Ligands: ZN, L8N, DMS
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Human Carbonic Anhydrase Vii In Complex With A Sulfonamide Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.94 Å Release Date: 2020-06-10 Classification: LYASE Ligands: ZN, L8N |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-06-10
Ligands: ZN, L8N
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Crystal Structure Of Human Carbonic Anhydrase Ii In Complex With (R)-4-(2-Benzylpiperazin-1-Yl)Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.32 Å Release Date: 2020-05-13 Classification: LYASE Ligands: ZN, GOL, K1W |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-05-13
Ligands: ZN, GOL, K1W
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Crystal Structure Of Human Carbonic Anhydrase Ii In Complex With (R)-4-(2-Benzyl-4-Methylpiperazin-1-Yl)Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.25 Å Release Date: 2020-05-13 Classification: LYASE Ligands: ZN, GOL, K45 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-05-13
Ligands: ZN, GOL, K45
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Crystal Structure Of Human Carbonic Anhydrase Isozyme Ii With 4-(4-Benzyl-1,4-Diazepane-1-Carbonyl)Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.44 Å Release Date: 2020-05-13 Classification: LYASE Ligands: ZN, GOL, K4H |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-05-13
Ligands: ZN, GOL, K4H
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The Crystal Structure Of Human Carbonic Anhydrase Ii In Complex With 4-(3-Benzylimidazolidine-1-Carbonyl)Benzenesulfonamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.44 Å Release Date: 2020-05-13 Classification: LYASE Ligands: ZN, K4B, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2020-05-13
Ligands: ZN, K4B, GOL
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Benzensulfonamides Bearing Spyrohydantoin Moieties Act As Potent Inhibitors Of Human Carbonic Anhydrases Ii And Vii And Show Neuropathic Pain Attenuating Effects
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.30 Å Release Date: 2019-06-12 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, M8J, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-06-12
Ligands: ZN, M8J, GOL
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Benzensulfonamides Bearing Spyrohydantoin Moieties Act As Potent Inhibitors Of Human Carbonic Anhydrases Ii And Vii And Show Neuropathic Pain Attenuating Effects
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.30 Å Release Date: 2019-06-12 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, M8S, GOL |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-06-12
Ligands: ZN, M8S, GOL
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Benzensulfonamides Bearing Spyrohydantoin Moieties Act As Potent Inhibitors Of Human Carbonic Anhydrases Ii And Vii And Show Neuropathic Pain Attenuating Effects
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.45 Å Release Date: 2019-06-12 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, GOL, M8V, SO4 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-06-12
Ligands: ZN, GOL, M8V, SO4
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Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target The Tumor-Associated Carbonic Anhydrase Isoforms Ix And Xii And Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.88 Å Release Date: 2018-11-28 Classification: LYASE/LYASE inhibitor Ligands: ZN, J3V |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-11-28
Ligands: ZN, J3V
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Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target The Tumor-Associated Carbonic Anhydrase Isoforms Ix And Xii And Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.21 Å Release Date: 2018-11-28 Classification: LYASE/LYAS INHIBITOR Ligands: ZN, J4D |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-11-28
Ligands: ZN, J4D
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Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target The Tumor-Associated Carbonic Anhydrase Isoforms Ix And Xii And Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.88 Å Release Date: 2018-11-28 Classification: LYASE/LYASE INHIBITOR Ligands: ZN, J3V |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-11-28
Ligands: ZN, J3V
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Bioreductive 4-Hydroxy-3-Nitro-5-Ureido-Benzenesulfonamides Selectively Target The Tumor-Associated Carbonic Anhydrase Isoforms Ix And Xii And Show Hypoxia-Enhanced Cytotoxicity Against Human Cancer Cell Lines.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.63 Å Release Date: 2018-11-28 Classification: LYASE/LYASE inhibitor Ligands: ZN, J3V |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2018-11-28
Ligands: ZN, J3V