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4B1F

Design of Inhibitors of Helicobacter pylori Glutamate Racemase as Selective Antibacterial Agents: Incorporation of Imidazoles onto a Core Pyrazolopyrimidinedione Scaffold to Improve Bioavailabilty

Summary for 4B1F
Entry DOI10.2210/pdb4b1f/pdb
Related2JFX 2JFY 2JFZ 2W4I
DescriptorGLUTAMATE RACEMASE, 5-methyl-3-(1-methyl-1H-imidazol-5-yl)-7-(2-methylpropyl)-2-(naphthalen-1-ylmethyl)-2H-pyrazolo[3,4-d]pyrimidine-4,6(5H,7H)-dione, D-GLUTAMIC ACID, ... (4 entities in total)
Functional Keywordsisomerase, improved bioavailability
Biological sourceHELICOBACTER PYLORI
Total number of polymer chains2
Total formula weight58243.67
Authors
Basarab, G.S.,Hill, P.,Eyermann, C.J.,Gowravaram, M.,Kack, H.,Osimoni, E. (deposition date: 2012-07-10, release date: 2012-07-18, Last modification date: 2018-05-02)
Primary citationBasarab, G.S.,Hill, P.,Eyermann, C.J.,Gowravaram, M.,Kack, H.,Osimoni, E.
Design of Inhibitors of Helicobacter Pylori Glutamate Racemase as Selective Antibacterial Agents: Incorporation of Imidazoles Onto a Core Pyrazolopyrimidinedione Scaffold to Improve Bioavailabilty.
Bioorg.Med.Chem.Lett., 22:5600-, 2012
Cited by
PubMed: 22877632
DOI: 10.1016/J.BMCL.2012.07.004
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.05 Å)
Structure validation

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数据于2024-04-24公开中

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