Search Count: 17
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Hmcl1 Inhibitor Complex
Organism: Homo sapiens
Method: SOLUTION NMR Release Date: 2019-05-22 Classification: APOPTOSIS/INHIBITOR Ligands: N8J |
Organism: Homo sapiens
Method: SOLUTION NMR
Release Date: 2019-05-22
Ligands: N8J
 |
Co-Crystal Structure Of Mcl1 With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2019-05-15 Classification: APOPTOSIS/INHIBITOR Ligands: LOD |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-05-15
Ligands: LOD
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Co-Crystal Structure Of Mcl1 With Inhibitor
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.40 Å Release Date: 2019-05-15 Classification: APOPTOSIS/INHIBITOR Ligands: LOJ |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-05-15
Ligands: LOJ
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Co-Crystal Structure Of Mcl1 With Inhibitor 10
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.60 Å Release Date: 2019-05-15 Classification: APOPTOSIS/INHIBITOR Ligands: N0J |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-05-15
Ligands: N0J
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Crystal Structure Of Mcl1 With Inhibitor 8
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.48 Å Release Date: 2019-05-15 Classification: APOPTOSIS/INHIBITOR Ligands: N0M |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-05-15
Ligands: N0M
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Crystal Structure Of Mcl1 With Inhibitor 7
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.70 Å Release Date: 2019-05-15 Classification: APOPTOSIS Ligands: N0P |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2019-05-15
Ligands: N0P
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Crystal Structure Of Btk Kinase Domain Complexed With 4-Tert-Butyl-N-(3-{8-[4-(4-Methyl-Piperazine-1-Carbonyl)-Phenylamino]-Imidazo[1,2-A]Pyrazin-6-Yl}-Phenyl)-Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2014-05-14 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 481, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-05-14
Ligands: 481, DMS
 |
Crystal Structure Of Btk Kinase Domain Complexed With 4-Methanesulfonyl-N-(3-{8-[4-(Morpholine-4-Carbonyl)-Phenylamino]-Imidazo[1,2-A]Pyrazin-6-Yl}-Phenyl)-Benzamide
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2014-05-14 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2V1 |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-05-14
Ligands: 2V1
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Crystal Structure Of Btk Kinase Domain Complexed With 1-[5-[3-(7-Tert-Butyl-4-Oxo-Quinazolin-3-Yl)-2-Methyl-Phenyl]-1-Methyl-2-Oxo-3-Pyridyl]-3-Methyl-Urea
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.55 Å Release Date: 2014-05-14 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2V2, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-05-14
Ligands: 2V2, DMS
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Crystal Structure Of Btk Kinase Domain Complexed With 6-Cyclopropyl-2-[3-[5-[[5-(4-Ethylpiperazin-1-Yl)-2-Pyridyl]Amino]-1-Methyl-6-Oxo-3-Pyridyl]-2-(Hydroxymethyl)Phenyl]-8-Fluoro-Isoquinolin-1-One
Organism: Homo sapiens
Method: X-RAY DIFFRACTION Resolution:1.95 Å Release Date: 2014-05-14 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 2V3, DMS |
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Release Date: 2014-05-14
Ligands: 2V3, DMS
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Hepatitis C Virus Polymerase Ns5B Genotype 1B (Bk) In Complex With Rg7109 (N-{4-[6-Tert-Butyl-5-Methoxy-8-(6-Methoxy-2-Oxo-2,5-Dihydropyridin-3-Yl)Quinolin-3-Yl]Phenyl}Methanesulfonamide)
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2014-05-07 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: ZN, 28L |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2014-05-07
Ligands: ZN, 28L
 |
Hepatitis C Virus Polymerase Ns5B Genotype 1B (Bk) In Complex With Compound 48 (N-({(3S)-1-[6-Tert-Butyl-5-Methoxy-8-(2-Oxo-1,2-Dihydropyridin-3-Yl)Quinolin-3-Yl]Pyrrolidin-3-Yl}Methyl)Methanesulfonamide)
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:2.30 Å Release Date: 2014-05-07 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: DMS, 28M |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2014-05-07
Ligands: DMS, 28M
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Hepatitis C Virus Polymerase Ns5B Genotype 1B (Bk) In Complex With Inhibitor 2 (3-(3-Tert-Butyl-4-Methoxyphenyl)Pyridin-2(1H)-One)
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:2.80 Å Release Date: 2013-10-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: MG, DMS, 28O |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2013-10-09
Ligands: MG, DMS, 28O
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Hepatitis C Virus Polymerase Ns5B Genotype 1B (Bk) In Complex With Inhibitor 4 (N-(4-{2-[3-Tert-Butyl-2-Methoxy-5-(2-Oxo-1,2-Dihydropyridin-3-Yl)Phenyl]Ethyl}Phenyl)Methanesulfonamide)
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:2.09 Å Release Date: 2013-10-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: DMS, 28Q, GOL |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2013-10-09
Ligands: DMS, 28Q, GOL
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Hepatitis C Virus Polymerase Ns5B Genotype 1B (Bk) In Complex With Inhibitor 12 (N-{2-[3-Tert-Butyl-2-Methoxy-5-(2-Oxo-1,2-Dihydropyridin-3-Yl)Phenyl]-1,3-Benzoxazol-5-Yl}Methanesulfonamide)
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2013-10-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 28R, GOL |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2013-10-09
Ligands: 28R, GOL
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Hepatitis C Virus Polymerase Ns5B Genotype 1B (Bk) In Complex With Inhibitor 13 (N-{2-[3-Tert-Butyl-2-Methoxy-5-(2-Oxo-1,2-Dihydropyridin-3-Yl)Phenyl]-1,3-Benzoxazol-5-Yl}Methanesulfonamide)
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:2.05 Å Release Date: 2013-10-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: GOL, 2AY, DMS |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2013-10-09
Ligands: GOL, 2AY, DMS
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Hepatitis C Virus Polymerase Ns5B Genotype 1B (Bk) In Complex With Inhibitor 14 (N-(4-{(E)-2-[3-Tert-Butyl-2-Methoxy-5-(3-Oxo-2,3-Dihydropyridazin-4-Yl)Phenyl]Ethenyl}Phenyl)Methanesulfonamide)
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION Resolution:1.90 Å Release Date: 2013-10-09 Classification: TRANSFERASE/TRANSFERASE INHIBITOR Ligands: 28V |
Organism: Hepatitis c virus
Method: X-RAY DIFFRACTION
Release Date: 2013-10-09
Ligands: 28V