Patent Application
20130129832
The present invention relates to a cognitive impairment ameliorant comprising as an active ingredient thereof nobiletin, an analog thereof or citrus fruit extract, and royal jelly.
In Japan where the size of the elderly population is continuing to grow, the prevention and treatment of cognitive impairment attributable to aging, including impairment of the ability to concentrate, memory recall, organizational ability, planning ability and problem-solving ability, and particularly the representative disease thereof in the form of Alzheimer's disease, is becoming an important issue.
Nobiletin is a polymethoxyflavonoid contained in numerous citrus fruits that has been reported to have an information transmission promoting action that manages memory as well as inhibits facillitation of learning disabilities, and is known to be useful as an ameliorant for Alzheimer's disease and other forms of cognitive impairment (Patent Documents 1 and 2).
Royal jelly is a substance secreted from the pharyngeal glands of young worker honeybees, and is consumed as nourishment by larvae that become queen bees as well as adult queen bees. This substance is the only energy source for queen bees during their entire life span, which is forty times longer than that of worker bees. In addition, royal jelly contains incomparably higher levels of vitamins, minerals and amino acids than ordinary honey, and is also known to be rich in protein and contain various nutrients. However, the effects of royal jelly on cognitive impairment are still unknown.
Patent Document 1: Japanese Unexamined Patent Publication No. 2002-60340
Patent Document 2: International Patent Publication No. W02005-082351
An object of the present invention is to provide a cognitive impairment ameliorant useful for the prevention or treatment of cognitive impairment, and particularly preferable for Alzheimer's disease.
As a result of conducting extensive studies, the inventors of the present invention found for the first time that a composition comprising nobiletin, an analog thereof or a citrus fruit extract, and royal jelly, demonstrates extremely superior effects in a learning disability model, thereby leading to completion of the present invention.
Namely, the present invention relates to:
obtaining 3-(4-benzyloxy-3-methoxyphenyl)-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)-propenone by reacting the resulting 3-(4-benzyloxy-3-methoxyphenyl)-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)-propenone in the presence of iodine, and
obtaining 2-(4-hydroxy-3-methoxyphenyl)-5,6,7,8-tetramethoxychromen-4-one by reacting the resulting 3-(4-benzyloxy-3-methoxyphenyl)-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)-propenone in the presence of hydrogen and palladium carbon.
The nobiletin used in the present invention comprises 5,6,7,8,3′,4′-hexamethoxyflavone, a pharmaceutically acceptable salt thereof, or a hydrate or solvate thereof.
The nobiletin of the present invention can be chemically synthesized using methods known among persons with ordinary skill in the art. In addition, it can also be extracted from plants of the citrus family. Extracts of members of the citrus family that contain nobiletin can also be used in the present invention. This includes, for example, the nobiletin analog, 4′-hydroxy-5,6,7,8,3′-pentamethoxyflavone (4-demethylated nobiletin), pharmacologically acceptable salts thereof, as well as hydrates or solvates thereof.
Examples of plants of the citrus family include Citrus depressa, Citrus unshiu, Citrus tangerina, Citrus erythrosa, Citrus aurantium, Citrus deliciosa, Citrus grandis, Citrus kinokuni, Citrus reticulata, Citrus tachibana and Citrus sunki.
The extract of a citrus family plant used in the present invention may be extracted from a plant in the natural state or dried state after harvesting. Examples of extracted sites include the fruit, skin, seeds, leaves, branches, roots or flowers of mature or immature. Extracts are preferable obtained from the fruit or skin.
There are no particular limitations on royal jelly able to be used in the present invention, and commercially available royal jelly can be used. The royal jelly is preferably a product manufactured by Japan Royal Jelly Co., Ltd. In the present invention, the royal jelly is royal jelly freeze-dried powder (FD powder) unless specifically indicated otherwise.
In the present invention, the content of nobiletin is 0.0025 to 2.00% by weight, preferably 0.005 to 1.50% by weight, and more preferably 0.01 to 1.00% by weight. On the other hand, in the case of using an extract comprising 10% nobiletin, the content of the extract is 0.025 to 20.0% by weight, preferably 0.05 to 15.0% by weight and more preferably 0.1 to 10.0% by weight. In addition, the content of royal jelly as royal jelly FD powder is 3 to 60% by weight, preferably 5 to 45% by weight and more preferably 10 to 30% by weight.
In the present invention, the ratio of the content of nobiletin to the content of royal jelly is 2:3 to 1:24000, preferably 3:10 to 1:9000 and more preferably 1:10 to 1:600. On the other hand, in the case of using an extract comprising 10% nobiletin, the ratio of the content of the extract to the content of royal jelly is 20:3 to 1:2400, preferably 3:1 to 1:900 and more preferably 1:1 to 1:60.
The cognitive impairment ameliorant of the present invention can be incorporated in a prescription drug, quasi drug or food and the like. In addition, a dendrite elongation agent of the present invention can be used by oral or parenteral administration.
Examples of forms of prescription drugs include tablets, capsules, granules or syrup. These prescription drugs can be produced by using additives normally used in the production of prescription drugs.
Although there are no particular limitations on the dosage of the cognitive impairment ameliorant of the present invention, in the case of oral administration, for example, the dosage is 10 to 60 mg/kg of body weight per day and preferably 20 mg/kg of body weight per day, while in the case of parenteral administration, the dosage if 2 to 6 mg/kg of body weight per day and preferably 2 to 3 mg/kg of body weight per day. The aforementioned dosages can be administered once per day or divided into 2 to 3 administrations per day, and the dosage can be suitably adjusted according to age, disease status and symptoms.
Specific examples of additives include lactose, dextrin, sucrose, mannitol, cornstarch, sorbitol, microcrystalline cellulose and polyvinyl pyrrolidone, and these additives can be used alone or in a suitable combination thereof. These prescription drugs can be produced using methods suitable for each drug form in accordance with that described in the Japanese Pharmacopeia. In addition, flavoring agents, colorants, sweeteners and the like can also be suitably used. The contents of these additives can be suitably selected by a person with ordinary skill in the art.
Examples of forms of quasi drugs include tablets, capsules, granules, jelly and drinks. These quasi drugs can be produced using additives normally used in the production of quasi drugs. Moreover, these quasi drugs can also contain other active ingredients such as vitamins. In addition, additives such as sweeteners, flavoring agents, colorants or antioxidants can also be used alone or in a suitable combination thereof. These quasi drugs can be produced by methods commonly known among persons with ordinary skill in the art.
Examples of the forms of foods include noodles, pasta, powders, tablets, jelly and liquids (beverages). These foods can be produced by suitably using various food materials. Specific examples of food materials include rice, wheat, corn, potatoes, sweet potatoes, soybeans, powdered seaweed, candy, lactose, glucose, fructose, sucrose and mannitol, and these can be used alone or in a suitable combination thereof. A desired form can be obtained by using water and the like as necessary. Moreover, additives such as flavoring agents, colorants, sweeteners, edible oils or vitamins can also be suitably added.
Although the following provides a detailed explanation of the present invention through examples thereof, these examples are only intended to be representative of the present invention, and the present invention is not limited thereto.
The cAMP/PKA/ERK/CREB-dependent signaling pathway has been demonstrated to be intimately involved in memory and learning ability of the brain. In recent years, nerve degeneration and neurological deficit attributable to accumulation of amyloid β protein (Aβ) in the brain, along with synaptic plasticity disorders accompanied by nerve cell death due to solubilizing Aβ, have come to be understood to be one of the factors of memory disorders associated with Alzheimer's disease (AD). For example, the long-term potentiation (LTP) of neural transmissions at hippocampal glutamate synapses, which is considered to be one of the cellular mechanisms of learning and memory formation, is a typical example of synapse plasticity. Aβ inhibits PKA/CREB signaling and is known to suppress the occurrence of this LTP. In other words, a food that contains a physiologically active substance capable of improving or suppressing inhibition of signaling by Ap in this manner is considered to be useful for the improvement and/or prevention of AD.
Therefore, the effects of royal jelly and the effects of the combined used of royal jelly and nobiletin on ERK activity in PC12D cells, which are considered to be model cells of nerve cells, were examined by western blotting using as an indicator thereof the effects of water-soluble components of “Royal Jelly FD Powder” on ERK phosphorylation.
1. Experimental Method
Culturing of PC12D Cells
PC12D cells (Aichi Prefectural County Research Institute) were sub-cultured using Dulbecco's Modified Eagle Medium (DMEM) comprising heat inactivated (56° C., 30 minutes) 5% horse serum (HS: Gibco), 10% fetal calf serum (FCS: CELLect), penicillin (50 units/mL) and streptomycin (50 pg/mL). The cells were cultured in an incubator maintained at 37° C. and comprising a mixture of 95% air and 5% CO2. Furthermore, in this experiment, medium prepared so as to contain 2% HS and 1% FCS was used to dilute the drug.
Preparation of “Royal Jelly FD Powder” Stock Solution (25%(w/v))
0.25 g of “Royal Jelly FD Powder” (Japan Royal Jelly Co., Ltd.) were weighed out into a sterilized 2 ml tube using a sterilized spatula. Subsequently, sterile PBS(−) was added to bring to a volume of 1 ml inside a laminar flow cabinet. After agitating, the solution was transferred to a refrigerator and allowed to stand undisturbed in a refrigerator overnight while repeating agitation every hour. After agitating on the following day, the solution was centrifuged for 10 minutes at 12000×g and 4° C. The supernatant was then sterilized by filtration and then stored frozen at −20° C. after dividing into individual aliquots.
Western Blotting
PC12D cells were inoculated into a 35 mm dish at 1×106 cells/dish, and after culturing for 24 hours in a CO2 incubator, the cells were treated with drug. After lysing the drug-treated cells with 90 μl of cell lysis solution (1 mM EDTA, 1% SDS, 10 mM NaF, 10 nM calyculin, 320 nM okadaic acid, 1 mM sodium orthovanadate, 1 mM p-APMSF, 10 μg/ml pepstatin, 10 μg/ml antipain, 10 μg/ml leupeptin, 10 μg/ml chymostatin, 10 μg/ml phorphoramidon and 10 mM HEPES (pH 7.5)), the lysate was recovered in a 1.5 ml tube and heated for 5 minutes at 95° C. Moreover, after subjecting to ultrasonic treatment for 5 minutes in ice water, the lysate was centrifuged for 20 minutes at 14,000 rpm followed by recovery of the supernatant and quantification of the amount of protein. Subsequently, SDS-PAGE sample buffer was added. Following SDS-PAGE, the protein was transferred to a PVDF membrane by western blotting followed by blocking for 2 hours using a blocking buffer (10 mM Tris-HCl, 100 mM NaCl, 0.05% Tween 20 and 5% skim milk: pH 7.4). Subsequently, the membrane was washed with TBST and incubated overnight at 4° C. with primary antibody diluted with blocking buffer. The membrane was further washed with TBST and incubated for 2 hours at room temperature with HRP-labeled IgG antibody diluted with blocking buffer followed by again washing with TBST. Bands were detected using the ECL method. Reprobing consisted of removing the antibody using stripping buffer (62.5 mM Tris-HCl, 2% SDS, 100 mM β-mercaptoethanol: pH 7.4) followed by detecting internal standard protein.
Data Analysis
Experiment values were shown as the mean±standard error. Student's t-test, analysis of variance and Dunnett's test were used for statistical processing, and a significant difference was judged to be present in the case of a level of significance of less than 5%.
2. Results
Effects of Royal Jelly and Nobiletin on ERK Phosphorylation in PC12D Cells
PC12D cells were inoculated into a 3.5 cm dish at 1×106 cells/dish and cultured overnight followed by treating for 15 minutes with low-serum medium comprising various drugs, and lysing the cells with cell lysis solution to obtain a cell extract. The expression levels of p-ERK and total ERK in the cell extract were then analyzed. Furthermore, the royal jelly solutions were used in the experiment after preparing a 25% solution and diluting with low-serum medium.
As a result, royal jelly remarkably promoted phosphorylation of ERK, which is an important constituent molecule of the cAMP/PKA/ERK/CREB-dependent signaling pathway that is known to play an important role in long-term potentiation of synaptic transmission, one of the cellular mechanisms of memory and learning, in PC12D cells at concentrations corresponding to dilution factors of 400-fold to 100-fold (0.0625 to 0.25% (w/v)) (
Effects of Nobiletin on Promotion of Royal Jelly-Induced ERK Phosphorylation in PC12D Cells
The following extremely interesting results were also obtained. Namely, 30 μM nobiletin, which only demonstrated weak promoting action of ERK phosphorylation when used alone, was determined to further enhance the remarkable ERK phosphorylation promoting activity of royal jelly. This finding strongly indicates the possibility that the combined use of royal jelly and nobiletin prominently promotes cAMP/PKA/ERK/CREB-dependent signaling intimately involved with memory and learning (
A study was conducted of the action of royal jelly alone or the combined use of royal jelly and nobiletin on cAMP/PKA/ERK/CREB-dependent signaling in PC12D cells. Culturing of PC12D cells and preparation of “Royal Jelly FD Powder” stock solution (25% (w/v)) were carried out in the same manner as previously described.
1. Experimental Method
Sub-culturing of Rat Hippocampal Neuronal Cells
A pregnant SD rat (E18) was sacrificed by cervical dislocation under ether anesthesia. After subsequently disinfecting the abdomen with 70% EtOH, the fetus was excised by making a midline incision in the abdomen. Moreover, the brain was excised from the rat fetus and the hippocampus was isolated using a stereo microscope. Culturing of hippocampal neuronal cells was carried out using the Sumitomo Nerve Cell Culture System manufactured by Sumitomo Bakelite Co., Ltd. The hippocampal tissue was dispersed with a dispersion solution comprising papain enzyme (Sumilon) and the supernatant was removed after centrifuging for 4 minutes at 1,000 rpm. The resulting pellet was dispersed with a dispersion solution (Sumilon), an isolation solution (Sumilon) was added to the cells after being adequately dispersed by pipetting, and the supernatant was removed after centrifuging for 5 minutes at 800 rpm. The resulting pellet was suspended using Neurobasal medium (comprising 500 ml of phenol red-free Neurobasal medium, 10 ml of 50× B-27 supplement, 0.5 mM L-glutamine and 0.005% penicillin-streptomycin), the suspension was inoculated into a polylysine-coated 48-well plate at 8×104 cells/well, and after culturing for 1 day, the cells were washed with PBS following by replacing with fresh medium and culturing with medium comprising 10 μM AraC by replacing half of the medium every 2 to 3 days.
Transfection and Reporter Gene Assay
PC12D cells were inoculated into a 48-well plate at 8×104 cells/well, and after culturing for 24 hours in growth medium, co-transfection was carried out using Lipofectamine® 2000 reagent (Invitrogen) at a concentration of pCRE reporter gene plasmid (firefly luciferase) of 0.1 μg/well and at a concentration of internal standard pRG-TK plasmid (Renilla mushroom luciferase) of 0.01 μg/well. 16 hours after transfection, the medium was replaced with medium comprising various drugs. After treating for 5 hours with medium comprising various concentrations of drugs, the medium was aspirated followed by lysing and recovering the cells by addition of passive lysis buffer (Dual-Luciferase Reporter Assay System, Cat. No. E1960 (Promega)). Furthermore, activities of the firefly and Renilla mushroom luciferases were measured with a luminometer (Mini Lumat LB9506 (Berthold)) using the Dual-Luciferase Reporter Assay System (Promega).
On the other hand, hippocampal neuronal cells prepared according to the method described above were cultured for 10 to 14 days with Neurobasal medium, transfected with reporter plasmid (0.1 μg/well) and Renilla mushroom pRG-TK plasmid (0.01 μg/well) by lipofection, and treated with drug for a fixed period of time. Measurement of transcription activity was carried out using the Dual-Luciferase® Reporter Assay System manufactured by Promega.
Statistical Analysis
Results obtained from the reporter gene assay were evaluated using one-way ANOVA (Tukey). The presence of a significant difference was tested based on a level of significance of 5% on both sides, and a significant difference was judged to be present in the case of a level of significance of less than 5%.
A study was made of the effects of combined use of royal jelly (RI) and nobiletin on CRE-dependent transcription in PC12D cells.
As shown in
Next, a study was made of the effects of combined use of royal jelly and citrus fruit extract on CRE-dependent transcription in PC12D cells.
As shown in
Moreover, a study was also conducted on the effects of nobiletin on CRE-dependent transcription in sub-cultured rat hippocampal neuronal cells.
As a result of examining the effects of nobiletin on CRE-dependent transcription using the reporter gene assay method, nobiletin was determined to concentration-dependently promote CRE-dependent transcription in hippocampal neuronal cells.
As shown in
The following provides an example of a method for producing 4-demethylated nobiletin. However, the method used to produce 4-demethylated nobiletin is not limited to the method described here.
A scheme for organic synthesis of 4-demethylated nobiletin is shown below.
After adding concentrated sulfuric acid (0.54 ml, 10.2 mmol) to an MeOH solution (20.4 ml, 0.5 M) of 3,4,5-trimethoxybenzaldehyde (2.0 g, 10.2 mmol) while cooling with ice, a 30% aqueous hydrogen peroxide solution (3.5 ml, 30.6 mmol) was added slowly. After stirring for 15 minutes at room temperature, a 10% aqueous sodium hydroxide solution and sodium sulfite were added while cooling with ice to stop the reaction. After washing an organic layer extracted with AcOEt with brine, the organic layer was dried with MgSO4 followed by distilling off the solvent under reduced pressure. The residue was subjected to a silica gel chromatography, and 3,4,5-trimethoxyphenol (1.08 g, 7.0 mmol, 58%) was obtained in the form of a colorless solid from a elution part of AcOEt/hexane (5:6 v/v).
Colorless plate (AcOEt/hexane): mp 145-147° C. IR (CHCl3): 3303, 1612, 1129 cm−1. 1H-NMR (400 MHz, CDCl3) δ: 6.09 (2H, s), 5.90 (1H, s), 3.79 (3H, s), 3.76 (6H, s). 13C-NMR (100 MHz, CDCl3) δ: 153.6, 152.7, 131.4, 93.0, 61.0, 55.9. MS m/z : 184 (M+). HRMS Calcd. for C9H12O4: 184.0736. Found: 184.0715.
2-iodoxybenzoic acid (IBX) (160 mg, 5.7 mmol) were added to a DMF solution (3.6 ml, 0.15 M) of 3,4,5-trimethoxyphenol (0.10 g, 0.54 mmol) at room temperature followed by stirring for 30 minutes. After adding 1% Pd/C (10 mg), the system was replaced with a hydrogen atmosphere followed by stirring for 1 day. After returning the system to an argon atmosphere, potassium carbonate (220 mg, 1.6 mmol) and dimethyl sulfate (0.13 ml, 1.4 mmol) were added, and after additionally stirring for 3 hours at room temperature, the reaction solution was filtered with Celite and the solvent was distilled off under reduced pressure. After washing the organic layer, obtained by extracting the residue with Et2O, with brine, the organic layer was dried with MgSO4 and the solvent was distilled off under reduced pressure. The residue was subjected to a silica gel chromatography, and 1,2,3,4,5-pentamethoxybenzene (42 mg, 0.18 mmol, 34%) was obtained in the form of a colorless solid from a elution part of AcOEt/hexane (5:7 v/v).
Colorless needle (hexane): mp 59-61° C. IR (CHCl3): 1108 cm−1. 1H-NMR (400 MHz, CDCl3) δ: 6.30 (1H, s), 3.95 (3H, s), 3.85 (6H, s), 3.83 (6H, s). 13C-NMR (100 MHz, CDCl3) δ: 149.1, 147.9, 136.7, 93.7, 61.4, 61.3, 56.5. MS m/z: 228 (M+). HRMS Calcd. for C11H16O5: 228.0998. Found: 228.0983. Anal. Calcd. for C11H16O5: C, 57.88. H, 7.07. Found: C, 57.77. H, 7.00.
2,6-dimethoxy[1,4]benzoquinone (10 g, 58.8 mmol) was added to an MeOH solution (100 ml, 0.59 M) of Raney nickel (3.5 g) followed by stirring for 6 hours at room temperature in a hydrogen atmosphere. The reaction solution was filtered with Celite and the solvent was distilled off under reduced pressure to obtain crude 2,6-dimethoxybenzene-1,4-diol.
Potassium carbonate (41 g, 297 mmol) and dimethyl sulfate (14 ml, 147 mmol) were added to an acetone solution (100 ml, <0.59 M) of crude 2,6-dimethoxybenzene-1,4-diol (<58.8 mmol) followed by additionally stirring for 3 hours while heating at reflux. After washing an organic layer extracted with AcOEt with brine, the organic layer was dried with MgSO4 followed by distilling off the solvent under reduced pressure. The residue was subjected to a silica gel chromatography, and 1,2,3,5-tetramethoxybenzene (11.5 g, 158.1 mmol, 99%) was obtained in the form of a colorless oil from a elution part of AcOEt/hexane (1:2 v/v).
Colorless oil IR (CHCl3): 2931, 1594, 1506, 1129 cm−1. 1H-NMR (400 MHz, CDCl3) δ: 6.15 (2H, s), 3.85 (6H, s), 3.79 (3H, s), 3.79 (3H, s). 13C-NMR (100 MHz, CDCl3) δ: 156.2, 153.7, 132.4, 91.7, 61.0, 56.1, 55.5. MS m/z : 198 (M+). HRMS Calcd. for C10H14O4: 198.0892. Found: 198.0885.
AlCl3 (26 g, 192 mmol) was added to an Et2O solution (200 ml, 0.29 M) of 1,2,3,5-tetramethoxybenzene (11.5 g, 58.1 mmol) while cooling with ice. AcCl (5.4 ml, 75.5 mmol) was then added slowly followed by stirring for 2 hours at room temperature. The reaction was stopped by adding water until the aluminum dissolved while cooling with ice. After washing an organic layer extracted with Et2O with brine, the organic layer was dried with MgSO4 followed by distilling off the solvent under reduced pressure. The residue was subjected to a silica gel chromatography, and T-hydroxy-3′,4′,6′-trimethoxyacetophenone (11.1 g, 49.1 mmol, 85%) was obtained in the form of a yellow solid from a elution part of AcOEt/hexane (1:1 v/v).
Yellow needle (AcOEt): mp 114-116° C. IR (CHCl3): 1626, 1587, 1126 cm−1. 1H-NMR (400 MHz, CDCl3) δ: 13.80 (1H, s), 5.97 (1H, s), 3.94 (3H, s), 3.90 (3H, s), 3.82 (3H, s), 2.62 (3H, s). 13C-NMR (100 MHz, CDCl3) δ: 203.7, 159.0, 158.8, 158.4, 130.5, 106.3, 86.4, 60.7, 55.9, 55.5, 33.2. MS m/z : 226 (M+). HRMS Calcd. for C11H14O5: 226.0841. Found: 226.0829. Anal. Calcd. for C11H14O5: C, 58.40. H, 6.24. Found : C, 58.37. H, 6.18.
An aqueous sodium hydroxide solution (40 ml, 48 mmol) was added to an MeOH solution (130 ml, 0.37 M) of 2-hydroxy-3′,4′,6′-trimethoxyacetophenone (1.08 g, 47.7 mmol) while cooling with ice followed by slowly adding a 6% aqueous hydrogen peroxide solution (82 ml, 143 mmol). After stirring for 30 minutes at room temperature, 10% hydrochloric acid and sodium sulfite were added while cooling with ice to stop the reaction. After washing an organic layer extracted with AcOEt with brine, the organic layer was dried with MgSO4 followed by distilling off the solvent under reduced pressure to obtain crude 3,4,6-trimethoxybenzene-1,2-diol in the form of a colorless solid.
Potassium carbonate (170 g, 1.2 mol) and dimethyl sulfate (22 ml, 239 mmol) were added to an acetone solution (150 ml) of crude 3,4,6-trimethoxybenzene-1,2-diol followed by heating at reflux for 3 hours. After washing an organic layer extracted with AcOEt with brine, the organic layer was dried with MgSO4 followed by distilling off the solvent under reduced pressure. The residue was subjected to a silica gel chromatography, and 1,2,3,4,5-pentamethoxybenzene (11.5 g, 158.1 mmol, 99%) was obtained in the form of inseparable mixture with dimethyl sulfate from a elution part of AcOEt/hexane (5:7 v/v).
AlCl3 (42 g, 313 mmol) was added to an Et2O solution (330 ml) of crude 1,2,3,4,5-pentamethoxybenzene while cooling with ice. Subsequently, AcCl (14 ml, 187.5 mmol) was added slowly followed by stirring for 2 hours at room temperature. The reaction was stopped by adding water until the aluminum dissolved while cooling with ice. After washing an organic layer extracted with Et2O with brine, the organic layer was dried with MgSO4 followed by distilling off the solvent under reduced pressure. The residue was subjected to a silica gel chromatography, and 2′-hydroxy-3′,4′,5′,6′-tetramethoxyacetophenone (4.5 g, 17.6 mmol, 37%) was obtained in the form of a yellow oil from a elution part of AcOEt/hexane (1:3 v/v).
Yellow oil. IR (CHCl3): 2985, 1621, 1409, 1064 cm−1. 1H-NMR (400 MHz, CDCl3) δ: 13.12 (1H, s), 4.08 (3H, s), 3.96 (3H, s), 3.86 (3H, s), 3.81 (3H, s), 2.68 (3H, s). 13C-NMR (100 MHz, CDCl3) δ: 204.2, 154.6, 153.7, 151.4, 138.0, 136.8, 110.4, 61.3, 61.2, 61.1, 61.0, 32.2. MS m/z: 256 (M+). HRMS Calcd. for C12H16O6: 256.0947. Found: 256.0963.
A 50% potassium hydroxide solution (0.37 ml, 3.3 mol) was dropped in an EtOH solution (5.0 ml, 0.19 M) of 4-benzyloxy-3-methoxybenzaldehyde (340 mg, 1.41 mmol) and T-hydroxy-3′,4′,5′,6′-tetramethoxyacetophenone (240 mg, 0.94 mmol) at room temperature. After stirring for 24 hours, the reaction was stopped by adding 10% hydrochloric acid while cooling with ice. After washing the organic layer with brine, the organic layer was dried with MgSO4 and the solvent was distilled off under reduced pressure. The residue was subjected to a silica gel chromatography, and 3-(4-benzyloxy-3-methoxyphenyl)-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)-propenone (0.32 mg, 0.66 mmol, 71%) was obtained in the form of a yellow solid from a elution part of AcOEt/hexane (1:2 v/v).
Yellow needle (AcOEt/hexane): mp 99-100° C. IR (CHCl3): 1626, 1509, 1408, 1259, 1055 cm−1. 1H-NMR (400 MHz, CDCl3) δ: 13.26 (1H, s), 7.82 (1H, d, J=15.6 Hz), 7.78 (1H, d, J=15.6 Hz), 7.45-7.31 (5H, m), 7.17 (1H, d, J=8.4 Hz), 7.16 (1H, s), 6.90 (1H, d, J=8.4 Hz), 5.21 (2H, s), 4.09 (3H, s), 3.95 (3H, s), 3.89 (3H, s), 3.87 (3H, s), 3.86 (3H, s). 13C-NMR (100 MHz, CDCl3) δ: 193.3, 154.8, 153.2, 150.7, 150.4, 149.6, 144.0, 138.3, 137.1, 136.4, 128.5, 128.4, 127.9, 127.1, 124.2, 122.8, 113.4, 111.0, 110.9, 70.8, 62.2, 61.6, 61.3, 61.0, 56.0. Anal. Calcd. for C22H28O8: C, 67.49. H, 5.87. Found : C, 67.28. H, 5.83.
Iodine (3 mg, 0.01 mmol) was added to a DMSO solution (1.5 ml, 0.13 M) of 3-(4-benzyloxy-3-methoxyphenyl)-1-(2-hydroxy-3,4,5,6-tetramethoxyphenyl)-propenone (95 mg, 0.20 mmol) at room temperature followed by stirring for 1.5 hours at 150° C. The reaction was then stopped by adding sodium sulfite while cooling with ice. After washing an organic layer extracted with Et2O with brine, the organic layer was dried with MgSO4 followed by distilling off the solvent under reduced pressure. The residue was subjected to a silica gel chromatography, and 2-(4-benzyloxy-3-methoxyphenyl)-5,6,7,8-tetramethoxychromen-4-one (79 mg, 0.16 mmol, 83%) was obtained in the form of a yellow solid from a elution part of AcOEt/hexane (3:1 v/v).
Slightly yellow plate (AcOEt/hexane): mp 109-111° C. IR (CHCl3): 1641, 1514, 1361 cm−1. 1H-NMR (400 MHz, CDCl3) δ: 7.49-7.32 (7H, m), 6.99 (1H, d, J=8.5 Hz), 6.60 (1H, s), 5.24 (2H, s), 4.10 (3H, s), 4.01 (3H, s), 3.98 (3H, s), 3.95 (6H, s). 13C-NMR (100 MHz, CDCl3) δ: 177.2, 160.8, 151.3, 150.9, 149.7, 148.3, 147.6, 144.0, 137.9, 136.2, 128.6, 128.0, 127.1, 124.2, 119.4, 114.8, 113.4, 108.9, 106.9, 70.9, 62.3, 62.0, 61.8, 61.7, 56.1. Anal. Calcd. for C27H26O8: C, 67.77. H, 5.48. Found : C, 67.55. H, 5.58.
2-(4-benzyloxy-3-methoxyphenyl)-5,6,7,8-tetramethoxychromen-4-one (79 mg, 0.17 mmol) was added to an EtOH solution (2 ml, 0.08 M) of Pd/C (8 mg) followed by stirring for 2 hours at room temperature in a hydrogen atmosphere. The reaction solution was filtered with Celite and the solvent was distilled off under reduced pressure. The residue was subjected to a silica gel chromatography, and G010 (64 mg, 0.17 mmol, 99%) was obtained in the form of a yellow solid from a elution part of AcOEt.
Colorless prism (AcOEt/hexane): mp 155-156° C. IR (CHCl3): 3201, 1634, 1515, 1355, 1076 cm−1. 1H-NMR (400 MHz, CDCl3) δ: 7.53 (1H, d, J=8.3 Hz), 7.40 (1H, s), 7.05 (1H, d, J=8.3 Hz), 6.60 (1H, s), 6.13 (1H, m), 4.09 (3H, s), 4.04 (3H, s), 3.97 (3H, s), 3.93 (6H, s). 13C-NMR (100 MHz, CDCl3) δ: 177.4, 161.2, 151.4, 149.1, 148.3, 147.6, 147.0, 144.0, 138.0, 123.4, 120.2, 115.1, 114.7, 108.2, 106.5, 62.2, 61.9, 61.7, 61.6, 56.0. Anal. Calcd. for C20H20O8 : C, 61.85. H, 5.19. Found : C, 61.72. H, 5.29.
In the synthesis method described above, the oxidative cyclization reaction of 2′-hydroxychalcone to flavone using I2/DMSO (flavone backbone synthesis) is described in A. M. S. Silva, D. C. G. A. Pinto and J. A. S. Cavaleiro, Tetrahedron Lett., 1994, 35, 5899-5092, the conversion of compound 1 to compound 2 (oxidation of aromatic aldehyde to phenol) is described in M. Matsumoto, H. Kobayashi and Y. Hotta, J. Org. Chem., 1984, 49, 4740, the conversion of compound 2 to compound 3 (synthesis of catechol from phenol) is described in D. Magdziak, A. A. Rodriguez, R. W. Van De Water and T. R. R. Pettus, Org. Lett., 2002, 4, 285-288, the alternative synthesis of compound 3 (scheme 2, synthesis of compound 3 from compound 4) is described in M. Tsukayama, Y. Kawamura, T. Ishizuka, S. Hayashi and F. Torii, Heterocycles, 2003, 60, 2775-2784, and the synthesis of compound 9 (Friedel-Crafts acetylation) is described in M. Tsukayama, E. Kusunoki, M.M. Hossain, Y. Kawamura and S. Hayashi, Heterocycles, 2007, 71, 1589-1600.
The following indicates recommended amounts of incorporated components in the case of using a product of the present invention as a health food. The following also indicates the recommended daily dietary intake of health food materials considered to be effective for cognitive impairment. However, only a portion of healthy foods shown and are not limited thereto.
Ginkgo biloba leaf extract
Rhodiola sacra extract
The following indicates an example of using a product of the present invention as a health food. Although essential ingredients consist of royal jelly and nobiletin, DHA (docosahexanoic acid), Rhodiola sacra extract, phosphatidyl serine or ferulic acid and the like may also be contained. Although the health food may be in any form, the following indicates the example of sugar-coated tablets.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2008-158085 | Jun 2008 | JP | national |
This application is a Divisional of, and claims priority to copending U.S. application Ser. No. 12/672,768 filed on Feb. 9, 2010, which is a National Phase of PCT International Application No. PCT/JP2009/060937 filed on Jun. 16, 2009, which claims priority under 35 U.S.C. §119(a) to Japanese Application No. 2008-158085 filed in Japan on Jun. 17, 2008. The entire contents of all of the above applications are hereby incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12672768 | Feb 2010 | US |
| Child | 13741846 | US |
