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Edithistory:Xeruborbactam

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oldid date/time username edit summary
1317671664 2025-10-19T10:25:57Z KylieTastic draft
1315192249 2025-10-05T09:41:18Z Boghog /* Clinical development */ added table of clinical trials
1315191653 2025-10-05T09:35:27Z Boghog /* Spectrum of activity */ wikify
1315191557 2025-10-05T09:34:30Z Boghog /* Mechanism of action */ wikify
1315191167 2025-10-05T09:30:09Z Citation bot Add: doi-access, article-number. Removed parameters. Some additions/deletions were parameter name changes. | [[:en:WP:UCB|Use this bot]]. [[:en:WP:DBUG|Report bugs]]. | Suggested by Headbomb | #UCB_toolbar
1315191102 2025-10-05T09:29:36Z Boghog copyedit to reduce the hype; added review article citation
1315190295 2025-10-05T09:22:05Z Boghog + graphics; added chemical categories
1315188813 2025-10-05T09:05:25Z Boghog added missing data to drug box
1315185809 2025-10-05T08:30:54Z Boghog consistent citation formatting; correct errors in drug box
1315080660 2025-10-04T19:27:37Z Mousumi701
1315079145 2025-10-04T19:18:10Z ChildrenWillListen Added {{[[Template:COI|COI]]}} tag
1315077003 2025-10-04T19:05:56Z Mousumi701
1315069397 2025-10-04T18:20:11Z ChildrenWillListen Added {{[[Template:COI|COI]]}} tag
1315069350 2025-10-04T18:19:53Z ChildrenWillListen [[WP:AFC|AFC]] draft
1315069346 2025-10-04T18:19:52Z ChildrenWillListen ChildrenWillListen moved page [[Xeruborbactam]] to [[Draft:Xeruborbactam]]: [[WP:DRAFTIFY|Not ready]] for mainspace, incubate in draftspace. See author's page creation log, etc. Reason/s: more sources needed, possible COI
1315060454 2025-10-04T17:14:51Z Mousumi701
1315057151 2025-10-04T16:53:02Z Mousumi701
1315057095 2025-10-04T16:52:37Z Mousumi701
1315056904 2025-10-04T16:51:28Z Mousumi701
1315056683 2025-10-04T16:50:01Z Mousumi701 [[WP:AES|←]]Created page with '** [[Xeruborbactam]], the first nanomolar β-lactamase inhibitor in clinical development, has very broad-spectrum efficacy against all Ambler classes (A–D), including OXA carbapenemases and metallo-enzymes. It is a boronic acid-based transition-state analogue that strongly inhibits carbapenemases with a Ki(app) of 4 nM, which is more effective than current inhibitors. Structural investigations showed that the cyclopropyl group covalently binds to Ser70 an...'