Compositions and methods for viral sensitization
US-2024360115-A1 · Oct 31, 2024 · US
US9468209B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9468209-B2 |
| Application number | US-201414548289-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 20, 2014 |
| Priority date | Sep 26, 2005 |
| Publication date | Oct 18, 2016 |
| Grant date | Oct 18, 2016 |
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.
A compound represented by formula (I), or (II), or a salt thereof, for eradicating weeds.
Opening claim text (preview).
What is claimed is: 1. A compound represented by formula (I), or (II), or a salt thereof, wherein R 1 independently and at each occurrence represents H; or —C k H 2k+1 , —OC k H 2k+1 , —(C═O)C k H 2k+1 , —COOC k H 2k+1 , —C k H 2k−1 , —OC k H 2k−1 , —(C═O)C k H 2k−1 , or —COOC k H 2k−1 , each unsubstituted or substituted by one or more substituents selected from a heterocycle, an aryl, a phenylalkyl, a heterocycloalkyl phenyl, a heterocycloalkyl, a heterocycloalkoxyl, a phenoxyl; a phenoxy phenyl; a halogen, a cyano, a nitro, an alkoxyalkyl, an alkoxycarbonyl, and/or an amido; wherein k represents an integer from 1 to 8; R 2 represents H, CH 3 — or CH 3 CH 2 —; and R 3 represents a straight or branched chain C n H 2n+1 , or C n H 2n−1 group which is substituted by a halogen group or a cyano group wherein n is an integer from 3 to 15. 2. A compound of claim 1 , represented by formula (III), (IV) or (V), or a salt thereof, wherein X independently and at each occurrence represents H; or —C m H 2m+1 , or —OC m H 2m+1 , each unsubstituted or substituted by one or more substituents selected from a heterocyclic alkyl, a heterocyclic aryl, an aryl, a phenylalkyl, a heterocycloalkyl phenyl, a heterocycloalkyl, a heterocycloalkoxyl, a phenoxyl; a phenoxy phenyl; a halogen, a cyano, a nitro, an alkoxyalkyl, an alkoxycarbonyl, and/or an amido; R 3 is a halogen, —CN, a phenyl, a halogenated alkyl, a cyano-alkyl, a phenylalkyl, a halogenoalkenyl, a cyanoalkenyl, or a phenylalkenyl; and m represents an integer from 1 to 7. 3. A herbicide composition for killing weeds, comprising an effective amount of the compound of claim 1 and a suitable additive. 4. A method of eradicating weeds, the method comprises applying to weeds selected from the group consisting of broadleaf weeds, grassy weeds, and sedge weeds an effective amount of a compound of claim 1 , or a salt thereof. 5. A method of eradicating weeds, comprises applying to weeds selected from the group consisting of broadleaf weeds, grassy weeds, and sedge weeds an effective amount of a herbicide composition of claim 3 . 6. The method of claim 4 , wherein the compound is applied in a solution having a concentration of 10-800 μg of the compound per 1 g of the solution. 7. The method of claim 4 , wherein the compound is applied under exposure to sun light. 8. The method of claim 4 , wherein the broadleaf weeds are crofton weeds.
2-Pyrrolones · CPC title
five-membered rings · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.