Compositions comprising amino lipid compounds and methods of making and use thereof

US2025032415A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2025032415-A1
Application numberUS-202218708499-A
CountryUS
Kind codeA1
Filing dateNov 9, 2022
Priority dateNov 11, 2021
Publication dateJan 30, 2025
Grant date

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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

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Disclosed herein are compositions comprising amino lipid compounds and methods of making and use thereof.

First claim

Opening claim text (preview).

1 . A composition comprising a compound defined by Formula I, or a pharmaceutically acceptable salt thereof: wherein R 10 is substituted or unsubstituted C 1 -C 5 alkyl; R 11 is substituted or unsubstituted C 1 -C 5 alkyl; R 12 , R 13 , and R 14 are each independently substituted or unsubstituted C 6 -C 20 alkyl; with the proviso that when R 10 is —C 5 H 10 — and R 11 is —C 3 H 6 —, then R 12 , R 13 , and R 14 are not all and with the proviso that when R 10 is —C 5 H 10 — and R 11 is —C 3 H 6 —, then R 12 , R 13 , and R 14 are not all 2 . (canceled) 3 . (canceled) 4 . (canceled) 5 . (canceled) 6 . The composition of claim 1 , wherein the compound is defined by Formula I-A: or a pharmaceutically acceptable salt thereof. 7 . (canceled) 8 . The composition of claim 1 , wherein the compound is defined by Formula I-B, or a pharmaceutically acceptable salt thereof: wherein n is an integer from 1 to 5. 9 . (canceled) 10 . (canceled) 11 . (canceled) 12 . The composition of claim 1 , wherein R 12 , R 13 , and R 14 are each independently a substituted or unsubstituted C 10 -C 18 alkyl. 13 . (canceled) 14 . (canceled) 15 . (canceled) 16 . (canceled) 17 . (canceled) 18 . Tag composition of claim 1 , wherein the compound is defined by Formula I-C, or a pharmaceutically acceptable salt thereof: wherein n is an integer from 1 to 4. 19 . The composition of claim 1 , wherein the compound is selected from the group consisting of: pharmaceutically acceptable salts thereof, and combinations thereof. 20 . (canceled) 21 . (canceled) 22 . (canceled) 23 . The composition of claim 1 , wherein the compound is selected from the group consisting of: pharmaceutically acceptable salts thereof, and combinations thereof. 24 . A composition comprising a compound defined by Formula II, or a pharmaceutically acceptable salt thereof: wherein R 15 is substituted or unsubstituted C 1 -C 5 alkyl; R 16 is substituted or unsubstituted C 1 -C 5 alkyl; R 17 , R 18 , and R 19 are each independently substituted or unsubstituted C 6 -C 20 alkyl; with the proviso that when R 15 is —C 5 H 10 — and R 16 is —C 3 H 6 —, then R 17 , R 18 , and R 19 are not all and with the proviso that when R 15 is —C 5 H 10 — and R 16 is —C 3 H 6 —, then R 17 , R 18 , and R 19 25 . (canceled) 26 . (canceled) 27 . (canceled) 28 . (canceled) 29 . The composition of claim 24 , wherein the compound is defined by Formula II-A: or a pharmaceutically acceptable salt thereof. 30 . (canceled) 31 . The composition of claim 24 , wherein the compound is defined by Formula II-B, or a pharmaceutically acceptable salt thereof: wherein m is an integer from 1 to 5. 32 . (canceled) 33 . (canceled) 34 . (canceled) 35 . The composition of claim 24 , wherein R 17 , R 18 , and R 19 are each independently a substituted or unsubstituted C 10 -C 18 alkyl. 36 . (canceled) 37 . (canceled) 38 . (canceled) 39 . (canceled) 40 . (canceled) 41 . The composition of claim 24 , wherein the compound is selected from the group consisting of: pharmaceutically acceptable salts thereof, and combinations thereof. 42 . (canceled) 43 . (canceled) 44 . The composition of claim 24 , wherein the compound is selected from the group consisting of: pharmaceutically acceptable salts thereof, and combinations thereof. 45 . A composition comprising a compound defined by Formula III, or a pharmaceutically acceptable salt thereof: wherein R 20 is substituted or unsubstituted C 1 -C 5 alkyl; and R 21 and R 22 are each independently substituted or unsubstituted C 6 -C 20 alkyl. 46 . (canceled) 47 . (canceled) 48 . (canceled)

Assignees

Inventors

Classifications

  • Amino acids, e.g. glycine, EDTA or aspartame · CPC title

  • Amines; Amides; Ureas; Quaternary ammonium compounds; Amino acids; Oligopeptides having up to five amino acids · CPC title

  • A61K9/1617Primary

    Organic compounds, e.g. phospholipids, fats · CPC title

  • Compounds having three or more nucleosides or nucleotides · CPC title

  • Oils, fats or waxes according to two or more groups of A61K47/02-A61K47/42; Natural or modified natural oils, fats or waxes, e.g. castor oil, polyethoxylated castor oil, montan wax, lignite, shellac, rosin, beeswax or lanolin (synthetic glycerides, e.g. medium-chain triglycerides, A61K47/14) · CPC title

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Frequently asked questions

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What does patent US2025032415A1 cover?
Disclosed herein are compositions comprising amino lipid compounds and methods of making and use thereof.
Who is the assignee on this patent?
Ohio State Innovation Foundation
What technology area does this patent fall under?
Primary CPC classification A61K9/1617. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Jan 30 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). 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).