NO donor compound, preparation method thereof, pharmaceutical composition comprising same, and use thereof

US12275686B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12275686-B2
Application numberUS-202418812980-A
CountryUS
Kind codeB2
Filing dateAug 22, 2024
Priority dateFeb 22, 2022
Publication dateApr 15, 2025
Grant dateApr 15, 2025

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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

Official abstract text for this publication.

Disclosed is NO donor compound and preparation method, pharmaceutical composition, and use. The compound has a structure represented by formula The NO donor compound and the pharmaceutical composition thereof, as hypoxia-activated NO donors, may be prepared as drugs for treating myocardial hypoxic damage disease. The prepared drugs can exert efficacy at both the cellular level and the animal level, and the synthesis method of the compound is simple and easy to operate.

First claim

Opening claim text (preview).

What is claimed is: 1. A NO donor compound, wherein a structure of the NO donor compound is represented by a formula I: wherein: when R1 is nitro group, R2 is selected from the group consisting of hydrogen, halogen, and C 1 -C 4 alkyl, R3 is selected from the group consisting of hydrogen, halogen, and C 1 -C 4 alkyl; or when R2 is selected from the group consisting of nitro group, R1 is hydrogen, halogen, and C 1 -C 4 alkyl, and R3 is selected from the group consisting of hydrogen, halogen, and C 1 -C 4 alkyl. 2. The NO donor compound of claim 1 , wherein in the formula I, R1 is nitro group, R2 is selected from the group consisting of hydrogen, halogen, and methyl, and R3 is hydrogen. 3. The NO donor compound of claim 1 , wherein the NO donor compound is selected from the group consisting of following compounds I1-I4: 4. A method for preparing the NO donor compound of claim 1 , comprising: obtaining the NO donor compound of formula I by acylation reaction between compound 1 and compound 2 as follows: 5. A pharmaceutical composition, comprising the NO donor compound of claim 1 and a pharmaceutically acceptable carrier.

Assignees

Inventors

Classifications

  • C07C243/06Primary

    N-nitroso-amines · CPC title

  • the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil · CPC title

  • A61P9/10Primary

    for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis · CPC title

  • Azo (—N=N—), diazo (=N2), azoxy (>N—O—N< or N(=O)—N<), azido (—N3) or diazoamino (—N=N—N<) compounds · CPC title

  • Preparation of compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes · CPC title

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What does patent US12275686B2 cover?
Disclosed is NO donor compound and preparation method, pharmaceutical composition, and use. The compound has a structure represented by formula The NO donor compound and the pharmaceutical composition thereof, as hypoxia-activated NO donors, may be prepared as drugs for treating myocardial hypoxic damage disease. The prepared drugs can exert efficacy at both the cellular level and the animal le…
Who is the assignee on this patent?
Univ Southeast
What technology area does this patent fall under?
Primary CPC classification C07C243/06. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Apr 15 2025 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).