Systems and methods for treatment of hearing using dihexa
US-2024424050-A1 · Dec 26, 2024 · US
US10111892B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10111892-B2 |
| Application number | US-201013513909-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 20, 2010 |
| Priority date | Dec 21, 2009 |
| Publication date | Oct 30, 2018 |
| Grant date | Oct 30, 2018 |
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The anti-cancer agent of the present invention contains at least one kind of phosphine transition metal complex selected from a group of compounds represented by the following Formulae (1a) to (1d). According to this anti-cancer agent, an anti-cancer agent is provided which has a higher anti-cancer activity and lower toxicity compared to anti-cancer agents in the related art. In Formulae (1a), (1b), (1c), and (1d), R 1 and R 2 represent a linear or branched alkyl group, and R 1 has a higher priority than R 2 as ranked according to RS notation. R 3 and R 4 represent a hydrogen atom or a linear or branched alkyl group. M represents an atom of a transition metal selected from a group consisting of gold, copper, and silver. X − represents an anion.
Opening claim text (preview).
The invention claimed is: 1. An anti-cancer agent comprising: at least one kind of phosphine transition metal complex selected from a group of compounds represented by Formulae (1a) to (1d), at least one kind of phosphine transition metal complex selected from a group of compounds represented by Formulae (2a) to (2c), and a phosphine transition metal complex represented by Formula (3), wherein in the Formulae, R 1 and R 2 represent a linear or branched alkyl group, a cycloalkyl group, a cycloalkyl group having a substituent, an adamantyl group, a phenyl group, or a phenyl group having a substituent that has 1 to 10 carbon atoms; R 1 and R 2 are different from each other, and R 1 has a higher priority than R 2 as ranked according to RS notation; R 3 and R 4 represent a hydrogen atom or a linear or branched alkyl group having 1 to 6 carbon atoms, and may be groups that are the same as or different from each other; R 3 and R 4 may form a saturated or unsaturated ring by binding to each other, and the saturated or unsaturated ring may have a substituent; M represents an atom of a transition metal selected from a group consisting of gold, copper, and silver; and X − represents an anion; and wherein the mixing ratio (molar ratio) among the total amount of the compounds represented by Formulae (1a) to (1d), the total amount of the compounds represented by Formulae (2a) to (2c), and the compound represented by Formula (3) is Formulae (1a) to (1d):Formulae (2a) to (2c):Formula (3)=20 to 80:10 to 30:10 to 80. 2. An anti-cancer agent comprising: at least one kind of phosphine transition metal complex selected from a group of compounds represented by Formulae (1a) to (1d), at least one kind of phosphine transition metal complex selected from a group of compounds represented by Formulae (2a) to (2c), and a phosphine transition metal complex represented by Formula (3), wherein in the Formulae, R 1 and R 2 represent a linear or branched alkyl group, a cycloalkyl group, a cycloalkyl group having a substituent, an adamantyl group, a phenyl group, or a phenyl group having a substituent that has 1 to 10 carbon atoms; R 1 and R 2 are different from each other, and R 1 has a higher priority than R 2 as ranked according to RS notation; R 3 and R 4 represent a hydrogen atom or a linear or branched alkyl group having 1 to 6 carbon atoms, and may be groups that are the same as or different from each other; R 3 and R 4 may form a saturated or unsaturated ring by binding to each other, and the saturated or unsaturated ring may have a substituent; M represents an atom of a transition metal selected from a group consisting of gold, copper, and silver; and X − represents an anion; and wherein the mixing ratio (molar ratio) among the total amount of the compounds represented by Formulae (1a) to (1d), the total amount of the compounds represented by Formulae (2a) to (2c), and the compound represented by Formula (3) is Formulae (1a) to (1d):Formulae (2a) to (2c):Formula (3)=40 to 70:5 to 25:15 to 50.
having the nitrogen atoms in the positions 1 and 4 · CPC title
having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate · CPC title
Six-membered rings · CPC title
Mouth and digestive tract, i.e. intraoral and peroral administration · CPC title
Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner (non-active ingredients are additionally classified in A61K47/00) · CPC title
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