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Search Count: 14

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3RTP image
Design And Synthesis Of Brain Penetrant Selective Jnk Inhibitors With Improved Pharmacokinetic Properties For The Prevention Of Neurodegeneration

4HZT image
Structure-Based Design Of Novel Dihydroisoquinoline Bace-1 Inhibitors That Do Not Engage The Catalytic Aspartates

4I0G image
Design And Synthesis Of Thiophene Dihydroisoquinolins As Novel Bace-1 Inhibitors

4I0Z image
Structure-Based Design Of Novel Dihydroisoquinoline Bace-1 Inhibitors That Do Not Engage The Catalytic Aspartates

4I10 image
Structure-Based Design Of Novel Dihydroisoquinoline Bace-1 Inhibitors That Do Not Engage The Catalytic Aspartates

4I11 image
Structure-Based Design Of Novel Dihydroisoquinoline Bace-1 Inhibitors That Do Not Engage The Catalytic Aspartates.

3QI1 image
Design And Synthesis Of Hydroxyethylamine (Hea) Bace-1 Inhibitors: Prime Side Chromane-Containing Inhibitors

3OY1 image
Highly Selective C-Jun N-Terminal Kinase (Jnk) 2 And 3 Inhibitors With In Vitro Cns-Like Pharmacokinetic Properties

3OXI image
Design And Synthesis Of Disubstituted Thiophene And Thiazole Based Inhibitors Of Jnk For The Treatment Of Neurodegenerative Diseases

3PTG image
Design And Synthesis Of A Novel, Orally Efficacious Tri-Substituted Thiophene Based Jnk Inhibitor

3N4L image
Bace-1 In Complex With Eln380842

3NSH image
Bace-1 In Complex With Eln475957
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.20 Å Release Date: 2010-09-22
Classification: HYDROLASE
Ligands: 957

3IVH image
Design And Synthesis Of Potent Bace-1 Inhibitors With Cellular Activity: Structure-Activity Relationship Of P1 Substituents
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:1.80 Å Release Date: 2010-01-05
Classification: HYDROLASE
Ligands: 1LI

3IVI image
Design And Synthesis Of Potent Bace-1 Inhibitors With Cellular Activity: Structure-Activity Relationship Of P1 Substituents
Organism: Homo sapiens
Method: X-RAY DIFFRACTION
Resolution:2.20 Å Release Date: 2010-01-05
Classification: HYDROLASE
Ligands: SO4, GOL, 2LI
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