Energy augmentation structures, energy emitters or energy collectors containing the same, and their use in solar cells and other energy conversion devices
US-2024115878-A1 · Apr 11, 2024 · US
US9867879B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9867879-B2 |
| Application number | US-201615004141-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 22, 2016 |
| Priority date | Jan 22, 2015 |
| Publication date | Jan 16, 2018 |
| Grant date | Jan 16, 2018 |
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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.
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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.
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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