Small molecule inhibitors selective for polo-like kinase protein

US12415822B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12415822-B2
Application numberUS-202318106543-A
CountryUS
Kind codeB2
Filing dateFeb 7, 2023
Priority dateApr 5, 2016
Publication dateSep 16, 2025
Grant dateSep 16, 2025

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Disclosed are small molecule PLK inhibitors that can target the polo box domain (PBD). Inhibitors can have an atomic mass of about 1000 Da or less and a general structure ofFor instance, the inhibitors can include an alkyl benzamido benzoic acid core structure.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for inhibiting Polo-like Kinase proteins, the method comprising: providing a small molecule PLK inhibitor to a medium containing one or more Polo-like Kinase proteins, wherein the small molecule PLK inhibitor has the following structure: wherein R 1 comprises an alkyl, —O-alkyl, —S-alkyl, or —NH-alkyl, and optionally includes a terminal aryl; R 7 is selected from: 2. The method of claim 1 , wherein the medium comprises a solution. 3. The method of claim 1 , wherein the medium comprises one or more cells. 4. The method of claim 1 , wherein the medium comprises one or more cells and the inhibitor induces apoptosis in a least a portion of the one or more cells. 5. The method of claim 1 , wherein the one or more Polo-like Kinase proteins comprise PLK1. 6. The method of claim 1 , wherein the one or more Polo-like Kinase proteins comprise PLK3. 7. The method of claim 3 , wherein the one or more cells comprise HeLa cervical cancer cells, PTEN-deficient prostate cancer (PC3) cells, KRAS mutant lung cancer (A-549) cells, or a combination thereof. 8. The method of claim 1 , wherein R 1 comprises a C10 to C12 alkyl. 9. The method of claim 1 , wherein the small molecule PLK inhibitor has an atomic mass of about 1000 Daltons or less. 10. The method of claim 1 , wherein the small molecule PLK inhibitor has an atomic mass of about 500 Daltons or less. 11. The method of claim 1 , wherein the small molecule PLK inhibitor has a polar surface area of about 200 Å or less. 12. The method of claim 1 , wherein the small molecule PLK inhibitor has a polar surface area of about 100 Å or less. 13. A method for inhibiting Polo-like Kinase proteins, the method comprising: providing a small molecule PLK inhibitor to a medium containing one or more Polo-like Kinase proteins, wherein the small molecule PLK inhibitor has the structure of one or more of:

Assignees

Inventors

Classifications

  • the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil · CPC title

  • having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol · CPC title

  • Antineoplastic agents · CPC title

  • specific for metastasis · CPC title

  • with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring · CPC title

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Frequently asked questions

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What does patent US12415822B2 cover?
Disclosed are small molecule PLK inhibitors that can target the polo box domain (PBD). Inhibitors can have an atomic mass of about 1000 Da or less and a general structure ofFor instance, the inhibitors can include an alkyl benzamido benzoic acid core structure.
Who is the assignee on this patent?
Univ South Carolina
What technology area does this patent fall under?
Primary CPC classification C07F9/222. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 16 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).