Process for producing pyridazinone compound and production intermediates thereof
US-2015376138-A1 · Dec 31, 2015 · US
US10544085B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10544085-B2 |
| Application number | US-201815919395-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 13, 2018 |
| Priority date | Mar 20, 2014 |
| Publication date | Jan 28, 2020 |
| Grant date | Jan 28, 2020 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Compounds, called liamocins from Aureobasidium pullulans , having the general structure in Formula 1 are disclosed. where R 1 is either COCH 3 or H; and R 2 is between two to ten O-linked 3,5-dihydroxydecanoate; and R 3 can be a polyol (e.g., L- or D-glycerol, L- or D-threitol, L- or D-erythritol, L- or D-arabitol, L- or D-xylitol, L- or D-lyxitol, L- or D-ribitol, L- or D-allitol, L- or D-altritol, L- or D-mannitol, L- or D-iditol, L- or D-gulitol, L- or D-glucitol (also called sorbitol), L- or D-galactitol (also called dulcitol), and L- or D-talitol), 2-amino-D-mannitol, 2N-acetylamino-D-mannitol, L-rhamnitol, or D-fucitol; except when R 3 is D-mannitol, R 2 is not 2 nor 3 O-linked 3,5-dihydroxydecanoate chains. These liamocins described above in addition to D-mannitol liamocin A1, D-mannitol liamocin A2, D-mannitol liamocin B1, and D-mannitol liamocin B2, alone or in combination with each other, can be used to kill certain bacteria and to treat certain bacterial infections.
Opening claim text (preview).
The invention claimed is: 1. A method of preventing a disease caused by S. agalactiae, S. infantarius, S. mitis, S. mutans, S. pneumonia, S. salivarius, S. suis , or S. uberis in an animal susceptible to said disease comprising administering an effective amount of a composition to prevent the growth of said S. agalactiae, S. infantarius, S. mitis, S. mutans, S. pneumonia, S. salivarius, S. suis , or S. uberis in or on said animal, wherein said composition comprises one or more of the compounds of Formula 1, optionally a carrier, and optionally a diluent; and wherein said Formula 1 is where R 1 is, independently, either COCH 3 or H; and R 2 is, independently, between two to ten O-linked 3,5-dihydroxydecanoate; and R 3 is, independently, one of the following: L- or D-glycerol, L- or D-threitol, L- or D-erythritol, L- or D-arabitol, L- or D-xylitol, L- or D-lyxitol, L- or D-ribitol, L- or D-allitol, L- or D-altritol, L- or D-mannitol, L- or D-iditol, L- or D-gulitol, L- or D-glucitol, L- or D-galactitol, L- or D-talitol, 2-amino-D-mannitol, 2N-acetylamino-D-mannitol, L-rhamnitol, or D-fucitol; and a combination thereof. 2. The method of claim 1 , wherein said compound of Formula 1 is selected from the group comprising L-mannitol liamocin A1, L-mannitol liamocin A2, L-mannitol liamocin B1, L-mannitol liamocin B2, D-mannitol liamocin A1, D-mannitol liamocin A2, D-mannitol liamocin B1, D-mannitol liamocin B2, L-arabitol liamocin A1, L-arabitol liamocin A2, L-arabitol liamocin B1, L-arabitol liamocin B2, D-arabitol liamocin A1, D-arabitol liamocin A2, D-arabitol liamocin B1, D-arabitol liamocin B2, L-threitol liamocin A1, L-threitol liamocin A2, L-threitol liamocin B1, L-threitol liamocin B2, D-threitol liamocin A1, D-threitol liamocin A2, D-threitol liamocin B1, D-threitol liamocin B2, L-glycerol liamocin A1, L-glycerol liamocin A2, L-glycerol liamocin B1, L-glycerol liamocin B2, D-glycerol liamocin A1, D-glycerol liamocin A2, D-glycerol liamocin B1, and D-glycerol liamocin B2. 3. The method of claim 1 , wherein said administering said composition occurs via topical administration, oral administration, or parenteral administration to said animal. 4. The method of claim 1 , wherein said animal is selected from the group consisting of a mammal, a bird, a fish, an amphibian, and a reptile.
Antivirals · CPC title
Esters of saturated alcohols having the esterified hydroxy group bound to an acyclic carbon atom · CPC title
Carboxylic acid esters · CPC title
esterified with hydroxy compounds having more than three hydroxy groups (esters of sugars C07H) · CPC title
of saturated hydroxy-carboxylic acids · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.