Methods for use of small molecule activators of hem-Y / protoporphyrinogen oxidase (PPO)

US9867879B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9867879-B2
Application numberUS-201615004141-A
CountryUS
Kind codeB2
Filing dateJan 22, 2016
Priority dateJan 22, 2015
Publication dateJan 16, 2018
Grant dateJan 16, 2018

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  1. Title

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  2. Abstract

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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.

A method for treating a microbial infection involves administering an effective amount of a compound of the formula: wherein R 1 is H, alkyl, aryl, heteroaryl, R 2 is H, halogen, alkyl, aryl, heteroaryl, R 3 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl, acetamide, R 4 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl, acetamide, R 5 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl, acetamide, R 6 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl, acetamide, R 7 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl, acetamide, R 8 is —CR 3 , O, S, wherein R 5 and R 6 , R 7 and R 6 , R 5 and R 4 , R 4 and R 3 can cyclize forming a 3-10 member ring comprising C, O, S, and/or N optionally substituted with one or more R 3 ; and administering light therapy, such as a photodynamic therapy (PDT) light source.

First claim

Opening claim text (preview).

What is claimed is: 1. A method for treating a gram-positive bacterial infection, comprising: activating protoporphyrinogen oxidase (PPO) in the gram-positive bacteria, thereby producing compounds via the heme biosynthetic pathway in the gram-positive bacteria, by administering an effective amount of a compound of the formula: wherein, R 1 is H, alkyl, aryl, heteroaryl; R 2 is H, halogen, alkyl, aryl, heteroaryl; R 3 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl, acetamide; R 4 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl, acetamide; R 5 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl, acetamide; R 6 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl, acetamide; R 7 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl, acetamide; R 8 is —CR 3 , O, S; wherein R 5 and R 6 , R 7 and R 6 , R 5 and R 4 , R 4 and R 3 can cyclize forming a 3-10 member ring comprising C, O, S, and/or N optionally substituted with one or more R 3 ; and administering light therapy. 2. The method of claim 1 , wherein: R 1 is H, alkyl, aryl; R 2 is H, halogen, alkyl, aryl, heteroaryl; R 3 is H, alkyl, hydroxyl, alkoxy, amino, amino sulfonyl, acetamide, aryl, heteroaryl; R 4 is H, alkyl, hydroxyl, alkoxy, amino, amino sulfonyl, acetamide; R 5 is H, alkyl, hydroxyl, alkoxy, amino, amino sulfonyl, acetamide; R 6 is H, alkyl, aryl. 3. The method of claim 1 , wherein R 1 is H, CH 3 , or R 2 is H, CH 3 , CH 2 CH 3 , R 3 is H, OH, R 4 is H, OH, or R 4 and R 5 , taken together with the carbon atoms to which they are bonded, can form an aromatic ring containing 6 carbon atoms; R 5 is H, OH, or R 4 and R 5 , taken together with the carbon atoms to which they are bonded, can form an aromatic ring containing 6 carbon atoms, or R 5 and R 6 , taken together with the carbon atoms to which they are bonded, can form an aromatic ring containing 6 carbon atoms; R 6 is H, or R 5 and R 6 , taken together with the carbon atoms to which they are bonded, can form an aromatic ring containing 6 carbon atoms; R 7 is H or OH; and R 8 is O or S. 4. The method of claim 1 , wherein the compound is selected from the compounds set forth in Table 1. 5. The method of claim 1 , wherein the compound is: 6. The method of claim 1 , wherein the compound is provided in a pharmaceutical composition. 7. The method of claim 1 , and further comprising administration of another compound or composition having microbial activity. 8. The method of claim 1 , wherein the compound is administered topically. 9. The method of claim 1 , wherein the light therapy uses light having a wavelength of about 380 nm.

Assignees

Inventors

Classifications

  • Screening for pharmacological compounds · CPC title

  • Photodynamic therapy, i.e. excitation of an agent · CPC title

  • for eliminating microbes, germs, bacteria on or in the body · CPC title

  • Polymorphic or mutational markers · CPC title

  • Protoporphyrinogen oxidase (1.3.3.4) · CPC title

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What does patent US9867879B2 cover?
A method for treating a microbial infection involves administering an effective amount of a compound of the formula: wherein R 1 is H, alkyl, aryl, heteroaryl, R 2 is H, halogen, alkyl, aryl, heteroaryl, R 3 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl, acetamide, R 4 is H, hydroxyl, alkoxy, alkyl, aryl, heteroaryl, amino, amino sulfonyl,…
Who is the assignee on this patent?
Univ Vanderbilt
What technology area does this patent fall under?
Primary CPC classification A61K41/0057. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Tue Jan 16 2018 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).