WO2016159604A2 - 코지산 유도체를 유효성분으로 포함하는 장수 유전자 활성화용 조성물 - Google Patents
코지산 유도체를 유효성분으로 포함하는 장수 유전자 활성화용 조성물 Download PDFInfo
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- WO2016159604A2 WO2016159604A2 PCT/KR2016/003116 KR2016003116W WO2016159604A2 WO 2016159604 A2 WO2016159604 A2 WO 2016159604A2 KR 2016003116 W KR2016003116 W KR 2016003116W WO 2016159604 A2 WO2016159604 A2 WO 2016159604A2
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- skin
- acid
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- klotho
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Definitions
- a longevity gene comprising kojic acid derivative as an active ingredient, specifically, a composition for activating Sirt-1, Klotho, XPD, ERCC8, FoxO3a gene.
- Retinoid refers to retinol, retinoic acid or derivatives thereof.
- Retinoids have a variety of biological effects, and skin-related effects have been reported on hyperkeratosis and acne, and retinoids such as retinol and retinoic acid have been known as external preparations for anti-aging (Dermatology therapy, 1998, 16, 357). 364).
- these retinoids have a positive effect and have a disadvantage in that irritation occurs even when only a small amount is applied to the skin, and because of their instability, they are easily oxidatively altered when exposed to air.
- studies to stabilize the retinoids continue to progress, but the stimulation to the skin, that is, the situation of safety has not yet been solved.
- aging research has been mainly focused on photoaging and endogenous aging.
- photoaging methods that can block ultraviolet rays, which are the main cause and prevent changes caused by UV irradiation, have been actively studied, and methods for mitigating endogenous aging caused by aging have been studied.
- Recently, research has been focused on finding ways to control the aging phenomenon. In particular, research on how to prevent aging and prolong life based on genetic research that controls the aging and life span of individuals.
- the present disclosure aims to provide a composition for activating the Sirt-1, Klotho, XPD, ERCC8, or FoxO3a gene, which is a longevity gene associated with anticancer or life extension.
- the present specification solves the problem of skin irritation, which is a problem of retinoids, and at the same time, a kojic acid derivative capable of specifically binding to the retinoic acid receptor (RAR), which is a receptor for retinoids, to solve the instability of the formulation as a skin external preparation.
- RAR retinoic acid receptor
- the disclosed technology is Sirt-1, Klotho, XPD, comprising a kojic acid derivative represented by the following formula (1), salts thereof, prodrugs thereof, hydrates thereof, solvates thereof or isomers thereof as an active ingredient
- a composition for activating one or more genes selected from the group consisting of ERCC8, and FoxO3a is provided.
- R 1 is -CH 2 -or -CH 2 CH 2-
- R 2 is -C (O) OCH 2-
- the kojic acid derivative may be cozyl methylene dioxycinnamate represented by the following formula (2).
- the kojic acid derivative, salt thereof, prodrug thereof, hydrate thereof, solvate thereof or isomer thereof may be included in 0.00001 to 10% by weight based on the total weight of the composition.
- the composition may be for enhancing expression of one or more proteins selected from the group consisting of Sirt-1, Klotho, XPD, ERCC8, and FoxO3a.
- the composition may be for anticancer.
- the composition may be for anticancer against skin cancer.
- the composition may be for extending the life.
- the composition may be for extending skin cell life.
- the skin cells may be dermal dermal derived fibroblasts.
- the composition may be for skin moisturizing or skin barrier strengthening.
- the composition may be a topical skin composition.
- the technology disclosed herein has the effect of providing a composition that activates the Sirt-1, Klotho, XPD, ERCC8, or FoxO3a gene, which is a longevity gene associated with anticancer or life extension.
- the technology disclosed herein can specifically bind to the retinoic acid receptor (RAR), a receptor for retinoids, to solve the skin irritation problem that is a problem of retinoids and at the same time solve the instability of the formulation as an external preparation for skin.
- RAR retinoic acid receptor
- the longevity gene Sirt-1, Klotho, XPD, ERCC8, or FoxO3a gene is activated to provide an effective skin improvement composition for prolonging skin cell life, moisturizing skin or strengthening skin barrier.
- Figure 1 is a photograph of the DAPI staining observation results of the control (control) not treated with seletinoid G in the test example of the present specification (Phase; transmitted light, DAPI; blue, FoxO3a; red, Merge; violet). The top photo and bottom photo show the results of two independent test runs.
- Figure 2 is a photograph of DAPI staining observation results of the test group treated with 15 ppm seletinoid G in the test example of the present specification (Phase; transmitted light, DAPI; blue, FoxO3a; red, Merge; violet). The top photo and bottom photo show the results of two independent test runs.
- Figure 3 is a photograph of DAPI staining observation results of the test group treated with 150 ppm seletinoid G in the test example of the present specification (Phase; transmitted light, DAPI; blue, FoxO3a; red, Merge; violet). The top photo and bottom photo show the results of two independent test runs.
- Figure 4 is a photograph of DAPI staining observation results of the test group treated with 450 ppm seletinoid G in the test example of the present specification (Phase; transmitted light, DAPI; blue, FoxO3a; red, Merge; violet). The top photo and bottom photo show the results of two independent test runs.
- Figure 5 is a graph showing the nuclear translocation (nuclear translocation rate) in the test example of the present specification, the control group 13.2%, seletinoid G 15 ppm treatment group 35.7 &, seletinoid G 150 ppm treatment group 86.3%, seletinoid In the G 450 ppm treatment group, 66.9% confirmed that the sentinoids activated the longevity gene FoxO3a significantly.
- the disclosed technology is Sirt-1, Klotho, XPD, comprising a kojic acid derivative represented by the following formula (1), salts thereof, prodrugs thereof, hydrates thereof, solvates thereof or isomers thereof as an active ingredient
- a composition for activating at least one gene selected from the group consisting of ERCC8, and FoxO3a is provided.
- R 1 is -CH 2 -or -CH 2 CH 2-
- R 2 is -C (O) OCH 2-
- the technology disclosed herein is one selected from the group consisting of gene activation, protein expression enhancement, anticancer, life extension, bioaging delay, bioaging symptoms improvement, skin hydration or skin barrier enhancement, and gene related disease improvement
- the technology disclosed herein is at least one selected from the group consisting of kojic acid derivatives represented by the formula (1), salts thereof, prodrugs thereof, hydrates thereof, solvates thereof and isomers thereof, or effective thereof
- Compositions for gene activation, protein expression enhancement, anti-cancer, life extension, bio-aging delayed, bio-aging symptoms improvement, skin moisturizing or skin barrier enhancement, or gene-related disease improvement comprising the components, Provided are methods for activating genes, enhancing protein expression, anticancer, prolonging life, delaying bioaging, improving symptoms of bioaging, enhancing skin moisturizing or skin barriers, or improving gene related diseases, including administration to a subject in need thereof.
- the techniques disclosed herein are for gene activation, for protein expression enhancement, for anticancer, for prolonging life, for delaying bioaging, for improving symptoms of bioaging, for moisturizing or for strengthening skin barriers, or for gene association
- kojic acid derivative represented by Formula 1 a salt thereof, a prodrug thereof, a hydrate thereof, a solvate thereof, and an isomer thereof are provided.
- the gene is at least one selected from the group consisting of Sirt-1, Klotho, XPD, ERCC8, and FoxO3a
- the protein is at least one protein selected from the group consisting of Sirt-1, Klotho, XPD, ERCC8, and FoxO3a.
- the cancer includes skin cancer, the life span includes the life span of the skin cells, the living body includes the skin, and the improvement includes any one or more of prevention, treatment, or improvement.
- the kojic acid derivative may be cozyl methylene dioxycinnamate represented by the following formula (2).
- salt or “pharmaceutically acceptable salt” means a salt according to one aspect of the invention that is pharmaceutically acceptable and has the desired pharmacological activity of the parent compound.
- the salt is formed from (1) an inorganic acid such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, or the like; Or acetic acid, propionic acid, hexanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, 3- (4-hydroxybenzoyl) Benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1,2-ethane-disulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, 4-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, 4-toluenesulfonic acid, camphorsulfonic acid, 4-methylbicyclo
- Suitable base salts are sodium, lithium, potassium, magnesium, aluminum, calcium, zinc, N, N'-dibenzylethylenediamine, chloroprocaine, choline, diethanolamine, ethylenediamine, N-methylglucosamine and pro Salts of cain.
- pharmaceutically acceptable means the approval of a government or equivalent regulatory body to use in animals, more specifically in humans, by avoiding significant toxic effects when used in conventional medicinal dosages. It can be received or approved, or listed in a pharmacopoeia or recognized as another general pharmacopeia.
- prodrug refers to a drug that modulates physical and chemical properties by chemically changing a drug, which itself does not exhibit physiological activity, but is originally produced by the action of a chemical or enzyme in the body after administration.
- the drug can be turned into a drug.
- prodrugs are converted into active drugs through chemical transformation through metabolic processes.
- such prodrugs are functional derivatives of the compounds of the invention and are readily converted into the desired compounds in vivo.
- conventional methods of selecting and preparing suitable prodrug derivatives are described in "Design Of Prodrugs", H Bund Saard, Elsevier, 1985. The entire contents of this document are incorporated herein by reference.
- hydrate refers to a compound to which water is bound, and is a broad concept including an inclusion compound having no chemical bonding force between water and the compound.
- solvate means a higher order compound produced between molecules or ions of a solute and molecules or ions of a solvent.
- isomers refers to a relationship of compounds having the same chemical formula but not identical, and isomers include structural isomers, geometric isomers, optical isomers, and stereoisomers.
- Structural isomers refer to compounds having the same molecular formula but different structures, and geometric isomers refer to isomers that differ in the spatial arrangement of atoms or groups of atoms bonded to two atoms connected by double bonds, and stereoisomers to Compounds having chemical constitution but differing in terms of the arrangement of atoms or groups in space;
- optical isomers (enantiomers) refer to two stereoisomers of a compound having mirror images that do not overlap one another; diastereomers are two or more A stereoisomer with an asymmetric center whose molecules are not mirror images of each other.
- isomers in particular are not only optical isomers (eg, essentially pure enantiomers, essentially pure diastereomers or mixtures thereof), but also form isomers ( conformation isomers (ie, isomers that differ only by their angles of one or more chemical bonds), position isomers (especially tautomers) or geometric isomers (eg, cis-trans isomers) do.
- essentially pure means at least about 90%, preferably at least about 95%, of a specific compound, for example enantiomers or diastereomers, when used in connection with an enantiomer or diastereomer. More preferably at least about 97% or at least about 98%, even more preferably at least about 99%, even more preferably at least about 99.5% (w / w).
- gene activation refers to facilitating the process by which certain genes on the DNA of a chromosome are transcribed and translated into proteins to reveal their function. In other words, by promoting the gene expression means that the transcription and translation process into the mRNA is active to ensure that the function of the gene is well expressed.
- the Sirt-1, Klotho, XPD, ERCC8, and FoxO3a genes are known as longevity genes associated with lifespan.
- SIRT1 sirtuin 1
- sirtuin 1 is a NAD + dependent deacetylase, wherein the human Sirt-1 gene is located at 69.64-69.68 Mb of chromosome 10, for example, having an mRNA sequence of NM_001142498. Moreover, it has a protein sequence of NP_001135970. It is known to be an enzyme that modulates protein function by deacetylating lysine residues of various proteins (Ageing Res, Vol. 1, pages 313-326, (2002)), and is known to have an effect of inhibiting the death of senescent cells.
- SIRT1 is involved in chromatin reconstitution, DNA damage responses, and dietary restriction associated with life extension associated with gene expression inhibition (Chen et al., Science 310, 1641, 2005). SIRT1 is also known to be involved in allergic respiratory diseases (J Allergy Clin Immunol. 2010 Feb; 125 (2): 449-460.e14. Doi: 10.1016 / j.jaci.2009.08.009.Epub 2009 Oct 27 .). SIRT1, like Sir2 in yeast, reconstructs chromatin and inhibits gene expression through histone deacetylation. In addition to histone proteins, SIRT1 induces deacetylation of various transcription factors related to cell growth, stress response, and endocrine control.
- Klotho is an enzyme produced by the KL gene, which produces type I membrane proteins associated with ⁇ -glucuronidase.
- the human klotho gene is located at 33.59-33.64 Mb of chromosome 13 and has an mRNA sequence of NM_004795, for example. It also has a protein sequence of NP_004786.
- Klotho gene knock-out mice rapidly increase in aging, and atherosclerosis, angiocalcification, soft tissue calcification, emphysema, decreased activity, and gonad formation associated with elevated levels of 1,25 (OH) 2D3 Abnormality, infertility, skin atrophy, ataxia, hypoglycemia and hyperphosphatemia (Mutation of the mouse klotho gene leads to a syndrome resembling ageing. Nature 1997; 390, 45-51). Conversely, increased klotho protein expression leads to increased lifespan, increased insulin resistance and increased IGF-1 resistance (Kurosu et al., 2005).
- Klotho's monobasic polymorphism also known as longevity gene, has been reported to be associated with shortening of life, osteoporosis, stroke and coronary artery disease (Arking et al., 2002, Kawano et al., 2002; Mullin et al. , 2005, Ogata et al., 2002; Yamada et al., 2005).
- high Klotho protein levels prolong brain cell lifespan, reduce the incidence of related diseases such as heart disease, enhance cognitive ability such as attention, memory, and cognition, and the lack of this protein promotes the aging process.
- XPD XPD (ERCC2; Excision repair cross-complementation group 2) protein is a member of a repair device that maintains DNA retention. This is one of the two enzymes involved in DNA unwinding, and along with other XP proteins, nucleotide cleavage repair, a type of DNA repair, causes XPD gene damage to cause a variety of skin diseases and aging (Mol Cell. 2003 Jun; 11). (6): 1635-46.).
- the human XPD gene is located at 45.85-45.87 Mb of chromosome 19 and has an mRNA sequence of NM_000400, for example. Moreover, it has a protein sequence of NP_000391.
- DNA repair defects accelerate aging and cause aging-related diseases (Best, BP (2009). "Nuclear DNA damage as a direct cause of aging”. Rejuvenation Research 12 (3): 199-208.) Risk of development (Bernstein C, Bernstein H, Payne CM, Garewal H. DNA repair / pro-apoptotic dual-role proteins in five major DNA repair pathways: fail-safe protection against carcinogenesis. Mutat Res. 2002 Jun; 511 (2): 145-78.Review.).
- XPD a DNA repair protein that affects these DNA repair defects, cause pigmentary dry skin, cocaine syndrome, and hair sulfur dystrophy.
- Pigmentary dry skin disease is a recessive gene photosensitive skin disease with a high incidence of skin cancer and is caused by genetic mutations involved in DNA repair.
- Cocaine syndrome is a form of dwarfism that is characterized by delayed growth, photosensitivity, and premature ejaculation. The disease is also known to be caused by defects in DNA repair genes, and genes that cause cocaine syndrome are also involved in protein production and are thought to be caused by abnormal accumulation and production of abnormal proteins in cells.
- Cocaine Syndrome a combination of dual pigmented dry skin syndrome.
- Hair sulfur dystrophy is a yellow-deficient hair dystrophy that causes hair to break and break well due to a lack of protein production, including sulfur. The common cause of these three diseases is known as XPD, one of the DNA repair proteins.
- Excision repair cross-complementation group 8 is also a protein that plays an important role in DNA repair.
- the human ERCC8 gene is located at 60.17-60.24 Mb of chromosome 5 and has an mRNA sequence of NM_000082, for example. It also has a protein sequence of NP_000073. Mutations in ERCC8 can lead to cocaine syndrome, a hereditary disease with premature aging. From this premature aging phenomenon, it can be seen that ERCC8 significantly affects aging.
- the FoxO3a gene is known as a longevity gene associated with lifespan.
- FoxO3a is a protein encoded by FoxO3 (Forhead box O3), which is known as a longevity gene, and is a transcription factor located in the insulin signaling pathway and is a protein that acts on expression of enzymes such as Mn-SOD and Catalase.
- the human FoxO3 gene is located at 108.88-109.01 Mb of chromosome 6 and has an mRNA sequence of NM_001455, for example. It also has a protein sequence of NP_001446.
- FoxO3 protein is also known as a cancer inhibitor (Myatt SS, Lam EW (November 2007). "The emerging roles of forkhead box (Fox) proteins in cancer”. Nat. Rev. Cancer 7 (11): 847-59.) . FoxO3 gene activity is associated with cancer development, and its degradation is often seen in cancer, and FoxO3 gene is known to be involved in inflammatory diseases following lymphocyte proliferation (Immunity 2004. 21: 203-213., Proc. Natl. Acad. Sci. 2004. 101: 2975-2980., Cell 1999. 96: 857-868).
- the kojic acid derivative, salt thereof, prodrug thereof, hydrate thereof, solvate thereof or isomer thereof is included in 0.00001 to 10% by weight based on the total weight of the composition, thereby having excellent efficacy and formulation without side effects. It may have stability. More specifically, the kojic acid derivative, salt thereof, prodrug thereof, hydrate thereof, solvate thereof or isomer thereof is 0.0001 to 5% by weight, more specifically 0.0005 to 3% by weight, more specifically based on the total weight of the composition It may be from 0.001 to 2% by weight.
- the composition may be for enhancing expression of one or more proteins selected from the group consisting of Sirt-1, Klotho, XPD, ERCC8, and FoxO3a.
- the composition may be for anticancer.
- the composition may be for cancer against the skin.
- the composition may be for prolonging life, delaying aging of the living body or improving symptoms of living aging.
- the composition may be for extending skin cell life.
- the skin cells may be dermal dermal derived fibroblasts.
- the composition may be for skin moisturizing or skin barrier strengthening.
- the composition may be for the prevention, amelioration or treatment of diseases associated with Sirt-1, Klotho, XPD, ERCC8, or FoxO3a gene.
- Sirt-1-related diseases are diseases caused by Sirt-1, such as a lack or inhibition of the Sirt-1 protein, an enzyme that deacetylates lysine residues of various proteins to regulate protein function, specifically cancer, diabetes, and degenerative nerves. Diseases, obesity, inflammatory diseases, allergic respiratory diseases, and the like.
- the degenerative neurological disease may be Alzheimer's, muscular dystrophy, axonal sclerosis, Parkinson's disease, Huntington's disease or multiple sclerosis, and the inflammatory disease is dermatitis, allergy, conjunctivitis, periodontitis, rhinitis, otitis media, sore throat, tonsillitis, pneumonia, gastric ulcer, duodenal ulcer , Hepatitis, esophagitis, gastritis, enteritis, pancreatitis, colitis, nephritis, arthritis, systemic edema, local edema.
- the inflammatory disease is dermatitis, allergy, conjunctivitis, periodontitis, rhinitis, otitis media, sore throat, tonsillitis, pneumonia, gastric ulcer, duodenal ulcer , Hepatitis, esophagitis, gastritis, enteritis, pancreatitis, colitis, nephritis, arthritis, systemic e
- Klotho-related diseases are diseases caused by klotho, such as lack of klotho protein, and specifically, cancer, arteriosclerosis, osteoporosis, stroke, and Alzheimer's disease.
- XPD-related diseases are diseases caused by XPD, a DNA repair protein that affects DNA repair defects, and specifically include cancer, pigmentary dry skin, cocaine syndrome, and hair sulfur dystrophy.
- ERCC8-related diseases are diseases caused by ERCC8, a DNA repair protein that affects DNA repair defects, and specifically include cancer and cocaine syndrome.
- FoxO3-related diseases are diseases caused by FoxO3 gene activity or inhibition, and include cancer, neurodegenerative diseases, and inflammatory diseases.
- degenerative neurological diseases include Alzheimer's disease, Parkinson's disease, Lou Gehrig's disease, Huntington's disease, multiple sclerosis, and the like.
- inflammatory diseases include dermatitis, allergies, conjunctivitis, periodontitis, rhinitis, otitis media, sore throat, tonsillitis, pneumonia, gastric ulcer, duodenal ulcer, hepatitis, esophagitis, gastritis, enteritis, pancreatitis, colitis, nephritis, arthritis, systemic edema, local edema, etc. Can be mentioned.
- the composition may be an external composition for skin, wherein the external composition for skin is used herein to include both pharmaceutical compositions and cosmetic compositions.
- the pharmaceutical composition may further comprise appropriate carriers, excipients and diluents commonly used in the manufacture of pharmaceutical compositions in one aspect.
- the carriers, excipients and diluents that may be included in the composition include lactose, dextrose, sucrose, sorbitol, mannitol, xylitol, erythritol, maltitol, starch, acacia rubber, alginate, gelatin, calcium phosphate, calcium silicate, Cellulose, methyl cellulose, microcrystalline cellulose, polyvinyl pyrrolidone, water, methylhydroxybenzoate, propylhydroxybenzoate, talc, magnesium stearate and mineral oil.
- the components included in the cosmetic composition may include components commonly used in cosmetic compositions in addition to kojic acid derivatives, salts thereof, prodrugs thereof, hydrates thereof, solvates thereof or isomers thereof as active ingredients, such as antioxidants, Conventional adjuvants such as stabilizers, solubilizers, vitamins, pigments, pigments and flavorings, and carriers.
- the cosmetic composition may be prepared in any formulation commonly prepared in the art, for example, solutions, suspensions, emulsions, pastes, gels, creams, lotions, powders, soaps, surfactant-containing cleansing, oils It may be formulated as powder foundation, emulsion foundation, wax foundation, spray, and the like, but is not limited thereto.
- Basic cosmetics such as powder, oil-in-water (O / W) or oil-in-water (O / W), makeup cosmetics such as lipstick, makeup base or foundation, cleaning agent such as shampoo, rinse, body cleanser, toothpaste or mouthwash It may be prepared in the form of a hair cosmetic such as hair tonic, gel or mousse, hair or hair dye.
- the carrier component is animal oil, vegetable oil, wax, paraffin, starch, tracant, cellulose derivative, polyethylene glycol, silicone, bentonite, silica, talc or zinc oxide, or the like. This can be used.
- the formulation of the cosmetic composition of the present disclosure is a powder or a spray
- lactose, talc, silica, aluminum hydroxide, calcium silicate or polyamide powder may be used as the carrier component, and in particular, in the case of a spray, additionally chlorofluorohydro Propellant such as carbon, propane / butane or dimethyl ether.
- a solvent, solubilizer or emulsion may be used as the carrier component, such as water, ethanol, isopropanol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate , Propylene glycol, butylene glycol, 1,3-butyl glycol oil, polyoxyethylene hardened castor oil, glycerol, glycerin, aliphatic ester, phenoxyethanol, triethanolamine, polyethylene glycol, beeswax, polysorbate 60, sorbitan Quiolade, paraffin, sorbitan stearate, lipophilic monostearic acid glycerine, stearic acid, glyceryl stearate / fig-400 stearate, carboxypolymer, cytosterol, polyglyceryl 2-oleate, ceramide, cholesterol, steares- 4,
- the carrier component such as water, ethanol, isopropanol
- a liquid diluent such as water, ethanol, butylene glycol or propylene glycol, ethoxylated isostearyl alcohol, polyoxyethylene sorbitol ester and polyoxyethylene sorbitan ester as carrier components
- Suspending agents such as, microcrystalline cellulose, hydroxyethyl cellulose, sodium hyaluronate, phenoxyethanol, aluminum meta hydroxide, bentonite, agar or tracant and the like can be used.
- the carrier component is an aliphatic alcohol sulfate, an aliphatic alcohol ether sulfate, a sulfosuccinic acid monoester, isethionate, an imidazolinium derivative, methyl taurate, sarcosinate.
- Cozymethylene dioxycinnamate 20mg, isomerized sugar 10g, mannitol 5g, a suitable amount of purified water was added to the purified water according to the conventional method for dissolving each component, and the lemon flavor was added appropriately, the above components were mixed and purified water was added to the whole After adjusting to 100ml to fill a brown bottle sterilized to prepare a liquid.
- Ointments were prepared in a conventional manner (% by weight) according to the compositions described below.
- Beta Glucan >................wave 7.0
- the nutritional lotion was prepared in a conventional manner according to the composition described below (% by weight).
- a nutritious cream was prepared in a conventional manner according to the composition described below (% by weight).
- NHF normal human fibroblast
- DMEM medium
- NHEKs normal human epidermal keratinocytes
- Lonza Allendale, NJ, USA
- KGM-GOLD Lonza, Allendale, NJ, USA
- keratinocyte growth medium KGM-GOLD, Lonza, Allendale, NJ, USA
- the kojic acid derivatives disclosed herein significantly increase the expression of Sirt-1, Klotho, XPD and ERCC8 genes known as longevity genes. That is, the kojic acid derivatives can be seen that activate the Sirt-1, Klotho, XPD and ERCC8 gene to activate their function to act as a longevity gene.
- the keratinocytes which make up most of the epidermis of the cells that make up human skin, are deeply involved in moisturizing, which inhibits skin moisture evaporation, and the barrier function that protects the skin from external harmful factors.
- the composition according to the present disclosure includes the kojic acid derivative as an active ingredient, and thus Sirt-1, Klotho, XPD and ERCC8 genes in keratinocytes that function as a barrier to protect skin from moisture and external harmful factors that inhibit skin moisture evaporation. It can be seen that there is a skin improvement effect useful for moisturizing the skin and strengthening the skin barrier by activating.
- the kojic acid derivative disclosed in the present specification activates the longevity genes Sirt-1, Klotho, XPD, and ERCC8, indicating that it has an effect of extending the lifespan of skin cells, specifically fibroblasts that occupy most of the dermis. Can be. This effect was found to be superior to retinol.
- human melanoma cells (Human MNT1 melanoma cells) were purchased from Lonza, and the effect of seletinoid G on the FoxO3a gene activation was investigated. It was confirmed by the nuclear translocation rate.
- seletinoid G was treated with human melanoma celloma at concentrations of 15, 150, and 450 ppm for 48 hours and stained with DAPI solution diluted at 1/10000 for 30 minutes, followed by Confocal Laser Scanning Microscope, Zeiss) was used to evaluate the degree of FoxO3a activation to the extent that red and blue fluorescence were superimposed in the nucleus and observed as violet fluorescence.
- the kojic acid derivative disclosed herein significantly increases the expression amount of FoxO3a gene known as longevity gene. That is, the kojic acid derivatives can be seen that activate the FoxO3a gene to activate its function to act as a cancer inhibitor, longevity gene.
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Abstract
Description
Claims (11)
- 제 1항에 있어서,상기 코지산 유도체, 이의 염, 이의 프로드럭, 이의 수화물, 이의 용매화물 또는 이의 이성질체는 조성물 총 중량을 기준으로 0.00001 내지 10 중량%로 포함되는, 조성물.
- 제 1항에 있어서,상기 조성물은 Sirt-1, Klotho, XPD, ERCC8, 및 FoxO3a로 이루어진 군에서 선택되는 1 이상의 단백질 발현 증진용인, 조성물.
- 제 1항에 있어서,상기 조성물은 항암용인, 조성물.
- 제 1항에 있어서,상기 조성물은 피부암에 대한 항암용인, 조성물.
- 제 1항에 있어서,상기 조성물은 수명 연장용인, 조성물.
- 제 7항에 있어서,상기 조성물은 피부 세포 수명 연장용인, 조성물.
- 제 8항에 있어서,상기 피부 세포는 피부 진피 유래 섬유아세포인, 조성물.
- 제 1항에 있어서,상기 조성물은 피부 보습용 또는 피부 장벽 강화용인, 조성물.
- 제 1항에 있어서,상기 조성물은 피부 외용제 조성물인, 조성물.
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US15/563,119 US10238624B2 (en) | 2015-03-31 | 2016-03-28 | Composition for activating longevity genes, containing kojic acid derivative as active ingredient |
JP2017551113A JP6799542B2 (ja) | 2015-03-31 | 2016-03-28 | コウジ酸誘導体を有効成分として含む長寿遺伝子活性化用組成物 |
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KR10-2015-0045129 | 2015-03-31 | ||
KR1020150045129A KR20160116831A (ko) | 2015-03-31 | 2015-03-31 | 코지산 유도체를 유효성분으로 포함하는 장수 유전자 활성화용 조성물 |
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CN115721575A (zh) * | 2022-05-10 | 2023-03-03 | 株式会社爱茉莉太平洋 | 缓和皮肤敏感性或者抑制皮脂分泌用组合物 |
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KR100483113B1 (ko) | 2002-09-17 | 2005-04-14 | 주식회사 태평양 | 코질-벤조산 유도체와 그 제조방법 및, 이를 함유하는화장료 조성물 |
KR101853718B1 (ko) | 2011-09-02 | 2018-05-03 | (주)아모레퍼시픽 | 코지산 유도체 제조 방법 |
CN102503908B (zh) * | 2011-11-22 | 2013-09-04 | 江苏省原子医学研究所 | 维a酸衍生物、其制备方法、其药物组合物及其在制备抗肿瘤药物中的应用 |
-
2016
- 2016-03-28 US US15/563,119 patent/US10238624B2/en active Active
- 2016-03-28 WO PCT/KR2016/003116 patent/WO2016159604A2/ko active Application Filing
- 2016-03-28 JP JP2017551113A patent/JP6799542B2/ja active Active
- 2016-03-28 CN CN201680024945.4A patent/CN107592810A/zh active Pending
- 2016-03-30 TW TW105110000A patent/TW201642851A/zh unknown
Also Published As
Publication number | Publication date |
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JP2018510182A (ja) | 2018-04-12 |
JP6799542B2 (ja) | 2020-12-16 |
WO2016159604A3 (ko) | 2016-12-08 |
TW201642851A (zh) | 2016-12-16 |
CN107592810A (zh) | 2018-01-16 |
US10238624B2 (en) | 2019-03-26 |
US20180078522A1 (en) | 2018-03-22 |
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