Pyridazinedione-based heterobicyclic covalent linkers and methods and applications thereof
US-2024425465-A1 · Dec 26, 2024 · US
US9745323B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9745323-B2 |
| Application number | US-201314418342-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 30, 2013 |
| Priority date | Jul 30, 2012 |
| Publication date | Aug 29, 2017 |
| Grant date | Aug 29, 2017 |
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The present invention provides a compound and a pharmaceutical composition for neuropsychological disorders or malignant tumors, the use of the compound and the pharmaceutical composition, or a method for preventing, improving, inhibiting the development of, and/or treating neuropsychological disorders or malignant tumors with the use of the compound and the pharmaceutical composition. One or more embodiments disclose a compound expressed by the following general formula (I) or (II) or a pharmaceutically acceptable salt of the compound:
Opening claim text (preview).
The invention claimed is: 1. A compound expressed by the following formula (I) or a prodrug of the compound or a pharmaceutically acceptable salt of the compound: wherein, in formula (I), R 1 and R 2 each independently represent a hydrogen atom or a C 1-6 hydrocarbon chain, R 3 represents where Z and atoms marked with a and b form a ring selected from the group consisting of one benzene ring, one heteroaromatic ring, an aromatic ring in which one or more benzene rings are condensed, a heteroaromatic ring in which one or more heteroaromatic rings are condensed, a mixed condensed polycyclic ring in which one or more benzene rings are condensed with one or more heteroaromatic rings, and a cyclic aliphatic, and the ring may have at least one substituent that is a hydrogen atom, a halogen atom, or a C 1-6 alkyl group, and R 4 represents a hydrogen atom, a halogen atom, or a C 1-6 alkyl group. 2. The compound according to claim 1 , said compound being or a prodrug of the compound or a pharmaceutically acceptable salt of the compound. 3. The compound according to claim 1 expressed by the following formula (III) or a prodrug of the compound or a pharmaceutically acceptable salt of the compound: wherein, in formula (III), R 7 and R 8 each independently represent a hydrogen atom, a halogen atom, or a linear or branched C 1-6 alkyl group. 4. The compound according to claim 1 , said compound being or a pharmaceutically acceptable salt of the compound. 5. A pharmaceutical composition containing the compound or the prodrug of the compound or the pharmaceutically acceptable salt of the compound according to claim 1 as an active ingredient. 6. A method for treating Down's syndrome, brain cancer, lung cancer, breast cancer, or Alzheimer's disease, said method comprising: administering a compound expressed by the following formula (I) or a prodrug of the compound or a pharmaceutically acceptable salt of the compound to a subject in need thereof: where, in the formula (I), R 1 and R 2 each independently represent a hydrogen atom or a C 1-6 hydrocarbon chain, R 3 represents where Z and atoms marked with a and b form a ring selected from the group consisting of one benzene ring, one heteroaromatic ring, an aromatic ring in which one or more benzene rings are condensed, a heteroaromatic ring in which one or more heteroaromatic rings are condensed, a mixed condensed polycyclic ring in which one or more benzene rings are condensed with one or more heteroaromatic rings, and a cyclic aliphatic, and the ring may have at least one substituent that is a hydrogen atom, a halogen atom, or a C 1-6 alkyl group, and R 4 represents a hydrogen atom, a halogen atom, or a C 1-6 alkyl group. 7. The method according to claim 6 , comprising: administering a compound expressed by or a prodrug of the compound or a pharmaceutically acceptable salt of the compound to a subject in need thereof. 8. The method according to claim 6 , comprising: administering a compound expressed by the following formula (III) or a prodrug of the compound or a pharmaceutically acceptable salt of the compound to a subject in need thereof: where, in the formula (III), R 7 and R 8 each independently represent a hydrogen atom, a halogen atom, or a linear or branched alkyl group. 9. The method according to claim 8 , comprising: administering a compound expressed by or a prodrug of the compound or a pharmaceutically acceptable salt of the compound to a subject in need thereof.
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