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Search Count: 33

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8C78 image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound Cct374705

7QK0 image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound 12A

6TOF image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound 4

6TOG image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound 5

6TOH image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound 6

6TOI image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound 11F

6TOJ image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound 17A

6TOK image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound 23D

6TOL image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound 25A

6TOM image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound 1

6TON image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound 25B

6TOO image
Crystal Structure Of Human Bcl6 Btb Domain In Complex With Compound 11A

6H3K image
Introduction Of A Methyl Group Curbs Metabolism Of Pyrido[3,4-D]Pyrimidine Mps1 Inhibitors And Enables The Discovery Of The Phase 1 Clinical Candidate Bos172722.
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.48 Å Release Date: 2018-09-19
Classification: TRANSFERASE
Ligands: FMW, 7PE

5EHL image
Rapid Discovery Of Pyrido[3,4-D]Pyrimidine Inhibitors Of Monopolar Spindle Kinase 1 (Mps1) Using A Structure-Based Hydridization Approach
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.66 Å Release Date: 2016-11-09
Classification: TRANSFERASE
Ligands: 0SQ

5EHO image
Rapid Discovery Of Pyrido[3,4-D]Pyrimidine Inhibitors Of Monopolar Spindle Kinase 1 (Mps1) Using A Structure-Based Hydridization Approach
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.18 Å Release Date: 2016-11-09
Classification: TRANSFERASE
Ligands: 5O1, DMS

5F4N image
Multi-Parameter Lead Optimization To Give An Oral Chk1 Inhibitor Clinical Candidate: (R)-5-((4-((Morpholin-2-Ylmethyl)Amino)-5-(Trifluoromethyl)Pyridin-2-Yl)Amino)Pyrazine-2-Carbonitrile (Cct245737)
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.91 Å Release Date: 2016-05-25
Classification: TRANSFERASE
Ligands: 5UY, EDO, GOL

5EH0 image
Rapid Discovery Of Pyrido[3,4-D]Pyrimidine Inhibitors Of Monopolar Spindle Kinase 1 (Mps1) Using A Structure-Based Hydridization Approach
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.18 Å Release Date: 2016-04-20
Classification: TRANSFERASE
Ligands: 5NW, DMS

5EHY image
Rapid Discovery Of Pyrido[3,4-D]Pyrimidine Inhibitors Of Monopolar Spindle Kinase 1 (Mps1) Using A Structure-Based Hydridization Approach
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.26 Å Release Date: 2016-04-20
Classification: TRANSFERASE
Ligands: 7PE, 5O4, EDO, DMS

5EI2 image
Rapid Discovery Of Pyrido[3,4-D]Pyrimidine Inhibitors Of Monopolar Spindle Kinase 1 (Mps1) Using A Structure-Based Hydridization Approach
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.67 Å Release Date: 2016-04-20
Classification: TRANSFERASE
Ligands: 5O7

5EI6 image
Rapid Discovery Of Pyrido[3,4-D]Pyrimidine Inhibitors Of Monopolar Spindle Kinase 1 (Mps1) Using A Structure-Based Hydridization Approach
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.01 Å Release Date: 2016-04-20
Classification: TRANSFERASE
Ligands: 5OQ, DMS
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