WO2022050634A1 - 펩타이드 및 이를 포함하는 화장료 조성물 및 약학 조성물 - Google Patents
펩타이드 및 이를 포함하는 화장료 조성물 및 약학 조성물 Download PDFInfo
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- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
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- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
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- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/575—Hormones
- C07K14/5759—Products of obesity genes, e.g. leptin, obese (OB), tub, fat
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1002—Tetrapeptides with the first amino acid being neutral
- C07K5/1005—Tetrapeptides with the first amino acid being neutral and aliphatic
- C07K5/101—Tetrapeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
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- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Definitions
- the present invention relates to a peptide and a cosmetic composition and pharmaceutical composition comprising the same.
- Skin aging is often caused by external and internal processes associated with an increase in skin wrinkles, sagging and sagging. Because external aging is mainly caused by repeated exposure to ultraviolet (UV) rays, it is generally referred to as 'photoaging'. . Naturally aged skin is smooth, pale, and finely wrinkled, but photoaging skin has thick skin wrinkles and causes pigmentation and telangiectasia.
- UV ultraviolet
- Subcutaneous fat plays an important role in maintaining energy homeostasis by secreting hormones and adipokines that control the metabolism of other tissues.
- the fat content of human subcutaneous adipose tissue is decreased by ultraviolet rays, which are environmental factors that cause various diseases such as photoaging, inflammation, immune suppression, and cancer, and adiponectin, a fat-derived product, is decreased in aged skin, and MMP-1 It is known to induce an increase in and a decrease in collagen.
- Sensitive skin refers to skin that reacts more sensitively than normal skin to external irritants, allergens, environmental changes, or internal causes of the human body, causing irritation reactions or dermatitis. There is also an example of treating sensitive skin by treating lactic acid or DMSO, which is known to cause dermatitis.
- Metabolic disease refers to a syndrome in which risk factors such as obesity, diabetes, high blood pressure, arteriosclerosis, and nonalcoholic fatty liver disease (NAFLD) appear together due to excessive nutrient accumulation in the body and lack of exercise. was officially named metabolic syndrome or insulin resistance syndrome through the Adult Treatment Program III established by the World Health Organization and the Heart, Lung, and Blood Institute of the US National Institutes of Health.
- adiponectin is a type of adipokine, a protein hormone specifically secreted from adipocytes, and regulates cardiovascular diseases such as hyperglycemia, hyperinsulinemia, obesity, and arteriosclerosis by enhancing the function of insulin and suppressing insulin resistance. plays an important role in
- adiponectin has a function of inhibiting cancer cell metastasis and inflammatory response.
- Adiponectin not only proliferates keratinocytes but also promotes the expression of filaggrin, hyaluronic acid and extracellular matrix in the skin, thereby performing wound healing, fibrosis inhibition, skin wrinkle improvement, and moisturizing.
- Adiponectin is composed of 244 amino acids and consists of a signal sequence, a collagen-like domain located at the N-terminal and a C1q-like globular domain located at the C-terminus.
- a hexamer and a 400 kDa polymer complex are major oligomers, and the polymer complex is known to have higher activity than the low molecular complex (LMW complex).
- An object of the present invention is to provide a peptide having excellent solubility and stability.
- An object of the present invention is to provide a cosmetic composition comprising the peptide.
- An object of the present invention is to provide a cosmetic composition for improving skin wrinkles, improving sensitive skin, improving dermatitis, or promoting hair growth, including the peptide.
- An object of the present invention is to provide a pharmaceutical composition for improving skin wrinkles, improving dermatitis, or promoting hair growth, including the peptide.
- An object of the present invention is to provide a pharmaceutical composition for the treatment of metabolic diseases comprising the peptide.
- a peptide consisting of the amino acid sequence of SEQ ID NO: 1 or 2 and having an amino group at the C-terminus.
- a cosmetic composition comprising the peptide of any one of 1 to 5 above.
- a pharmaceutical composition for improving skin wrinkles, improving dermatitis, or promoting hair growth comprising the peptide of any one of 1 to 5 above.
- a pharmaceutical composition for treating metabolic diseases comprising the peptide of any one of 1 to 5 above.
- the present invention relates to a peptide and a cosmetic composition and a pharmaceutical composition comprising the same, and has excellent solubility and stability, so it is advantageous for formulation when manufacturing a cosmetic or drug containing the same, thereby improving skin wrinkles, sensitive skin and dermatitis, promoting hair growth and The drug efficacy for metabolic diseases can be improved.
- 1 is a cell permeability test result of the peptide of the present invention.
- Figure 4 confirms the in vitro AMPK-phosporylation activity of the peptide of the present invention.
- 5 to 7 are results of experiments on the efficacy of the peptide of the present invention for promoting adiponectin production, procollagen and p-AMPK expression.
- FIG. 8 is a view confirming the ability of the peptide of the present invention to inhibit hepatocellular fat accumulation.
- 9 to 10 are results of experiments on the efficacy of the peptide of the present invention for improving sensitive skin and dermatitis.
- the present invention provides a peptide comprising the amino acid sequence of SEQ ID NO: 1 or 2 and having an amino group at the C-terminus.
- the peptide of the present invention consists of the amino acid sequence of SEQ ID NO: 1 (LYYF) or SEQ ID NO: 2 (GLYYF) and has an amino group at the C-terminus. Toxicity and stability are improved.
- the peptide may be one in which at least one amino acid is D-form. At this time, regardless of the position of the amino acid, if at least one amino acid is D-form, the above effect can be achieved.
- the peptide of the present invention can be prepared by general chemical synthesis, for example, solid-phase peptide synthesis, and by culturing a microorganism transformed with a recombinant vector containing the nucleic acid encoding the peptide. After expressing the peptide, it may be prepared by purification by a conventional method, but is not limited thereto.
- the present invention may include functional equivalents and variants of a peptide comprising the amino acid sequence of SEQ ID NO: 1 or 2 and having an amino group at the C-terminus.
- the functional equivalent of the peptide includes a peptide that does not change the activity of the peptide as a whole, and a peptide capable of performing the same functionally is included in the scope of the present invention.
- the variant means, for example, one or several amino acids deleted, substituted or added in the amino acid sequence, and has 95% or more, preferably 98% or more, more preferably 99% or more identity to the amino acid sequence. say things, etc.
- identity refers to the number of amino acid residues in one amino acid sequence, including the number of gaps, when aligning (alignment) to the highest degree of identity with or without introducing a gap into the two amino acid sequences.
- “several” means an integer of 2 to 10, for example, an integer of 2 to 7, 2 to 5, 2 to 4, or 2 to 3.
- Specific examples of the natural variant include variants based on polymorphisms such as SNP (single nucleotide polymorphism), splice variants, and the like.
- the substitution is a conservative amino acid substitution. This is because if it is a conservative amino acid substitution, it may have a structure or property substantially equivalent to that of a peptide having the amino acid sequence.
- Conservative amino acids are mutually non-polar amino acids (glycine, alanine, phenylalanine, valine, leucine, isoleucine, methionine, proline, tryptophan) and polar amino acids (amino acids other than non-polar amino acids), charged amino acids (acidic amino acids (aspartic acid, glutamic acid) and basic Amino acids (arginine, histidine, lysine) and uncharged amino acids (amino acids other than charged amino acids), aromatic amino acids (phenylalanine, tryptophan, tyrosine), branched amino acids (leucine, isoleucine, valine) and aliphatic amino acids (glycine, alanine, leucine) , isoleucine, valine) and the like are known.
- it may include a peptide in which structural stability to heat, pH, etc. of the peptide is increased or peptide activity is increased due to mutation or modification in the amino acid sequence.
- the present invention provides a peptide comprising the amino acid sequence of SEQ ID NO: 1 or 2, wherein at least one amino acid is D-form.
- the peptide of the present invention consists of the amino acid sequence of SEQ ID NO: 1 (LYYF) or SEQ ID NO: 2 (GLYYF), and at least one amino acid is D-form, solubility, cell permeability, and cell Toxicity and stability are improved.
- the peptide may be one in which one amino acid is D-form. At this time, regardless of the position of the amino acid, if one amino acid is D-form, the above effect can be achieved.
- the peptide of the present invention can be prepared by general chemical synthesis, for example, solid-phase peptide synthesis, and by culturing a microorganism transformed with a recombinant vector containing the nucleic acid encoding the peptide. After expressing the peptide, it may be prepared by purification by a conventional method, but is not limited thereto.
- the present invention may include functional equivalents and variants of a peptide consisting of the amino acid sequence of SEQ ID NO: 1 or 2, wherein at least one amino acid is D-form.
- the functional equivalent of the peptide includes a peptide that does not change the activity of the peptide as a whole, and a peptide capable of performing the same functionally is included in the scope of the present invention.
- the variant means, for example, one or several amino acids deleted, substituted or added in the amino acid sequence, and has 95% or more, preferably 98% or more, more preferably 99% or more identity to the amino acid sequence. say things, etc.
- identity refers to the number of amino acid residues in one amino acid sequence, including the number of gaps, when aligning (alignment) to the highest degree of identity with or without introducing a gap into the two amino acid sequences.
- “several” means an integer of 2 to 10, for example, an integer of 2 to 7, 2 to 5, 2 to 4, or 2 to 3.
- Specific examples of the natural variant include variants based on polymorphisms such as SNP (single nucleotide polymorphism), splice variants, and the like.
- the substitution is a conservative amino acid substitution. This is because if it is a conservative amino acid substitution, it may have a structure or property substantially equivalent to that of a peptide having the amino acid sequence.
- Conservative amino acids are mutually non-polar amino acids (glycine, alanine, phenylalanine, valine, leucine, isoleucine, methionine, proline, tryptophan) and polar amino acids (amino acids other than non-polar amino acids), charged amino acids (acidic amino acids (aspartic acid, glutamic acid) and basic Amino acids (arginine, histidine, lysine) and uncharged amino acids (amino acids other than charged amino acids), aromatic amino acids (phenylalanine, tryptophan, tyrosine), branched amino acids (leucine, isoleucine, valine) and aliphatic amino acids (glycine, alanine, leucine) , isoleucine, valine) and the like are known.
- it may include a peptide in which structural stability to heat, pH, etc. of the peptide is increased or peptide activity is increased due to mutation or modification in the amino acid sequence.
- the present invention provides a cosmetic composition comprising the peptide.
- the cosmetic composition of the present invention may be for improving skin wrinkles, improving sensitive skin, improving dermatitis, or promoting hair growth.
- the sensitive skin may refer to skin showing various hypersensitivity reactions due to deterioration or abnormality in skin physiological function due to external or internal factors. Specifically, it refers to skin that exhibits symptoms such as dry skin, rough skin, stinging, itching, allergic reactions, redness and erythema due to skin irritants that do not respond to non-sensitive skin, lack of sleep, overwork, changing seasons, or stress. can
- the dermatitis may include a variety of inflammatory diseases appearing on the skin, for example, psoriatic dermatitis, dry dermatitis, atopic dermatitis, seborrheic dermatitis, contact dermatitis and molar dermatitis may include, but is not limited thereto.
- improvement refers to any process in which the symptoms are improved to some extent due to the cosmetic composition of the present invention, and may mean prevention, alleviation, and the like.
- the hair growth promotion includes other terms used in the art, such as wool or hair growth promotion, and may mean preventing or alleviating hair loss.
- the cosmetic composition containing the peptide of the present invention may include components commonly used in the cosmetic composition, for example, conventional adjuvants such as antioxidants, stabilizers, solubilizers, vitamins, pigments and fragrances, and carriers.
- conventional adjuvants such as antioxidants, stabilizers, solubilizers, vitamins, pigments and fragrances, and carriers.
- Products to which the composition can be added include, for example, astringent lotion, softening lotion, nourishing lotion, various creams, essence, pack, foundation, etc. , but not limited thereto.
- compositions of the present invention include skin lotion, skin softener, skin toner, astringent, lotion, milk lotion, moisture lotion, nourishing lotion, massage cream, nourishing cream, moisture cream, hand cream, essence, nourishing essence, pack, It includes formulations such as soap, shampoo, cleansing foam, cleansing lotion, cleansing cream, body lotion, body cleanser, emulsion, lipstick, makeup base, foundation, press powder, loose powder, eye shadow, conditioner, gel, wax, mist, etc. , but not necessarily limited thereto.
- the composition may be formulated by containing the peptide inside the nanoliposome and stabilizing it.
- the peptide When the peptide is contained inside the nanoliposome, the components of the peptide are stabilized to solve problems such as precipitation and deformation during formulation, and the solubility and percutaneous absorption of the component can be increased, thereby maximizing the efficacy expected from the peptide. can be expressed.
- the present invention provides a pharmaceutical composition comprising the peptide.
- the pharmaceutical composition of the present invention may be used to improve skin wrinkles, improve dermatitis, promote hair growth, or treat metabolic diseases.
- the dermatitis may include, for example, psoriatic dermatitis, dry dermatitis, atopic dermatitis, seborrheic dermatitis, contact dermatitis and molar dermatitis, but is not limited thereto.
- improvement refers to any process in which the symptoms are improved to some extent due to administration of the pharmaceutical composition of the present invention, and may mean prevention, alleviation, treatment, and the like.
- the hair growth promotion includes other terms used in the art to promote hair growth or hair growth, and may mean preventing or treating hair loss.
- Metabolic disease may be, for example, obesity, diabetes, complications of diabetes, fatty liver, dyslipidemia, insulin resistance, cardiovascular disease, arteriosclerosis, hyperglycemia, hyperlipidemia or abnormal carbohydrate metabolism, but is not limited thereto.
- the pharmaceutical composition comprising the peptide of the present invention may further include a pharmaceutically acceptable carrier, and may be formulated together with the carrier.
- a pharmaceutically acceptable carrier refers to a carrier or diluent that does not stimulate the organism and does not inhibit the biological activity and properties of the administered compound.
- Acceptable pharmaceutical carriers for compositions formulated as liquid solutions include sterile and biocompatible, saline, sterile water, Ringer's solution, buffered saline, albumin injection, dextrose solution, maltodextrin solution, glycerol, ethanol and One or more of these components may be mixed and used, and other conventional additives such as antioxidants, buffers, and bacteriostats may be added as needed.
- diluents such as an aqueous solution, suspension, emulsion, etc., pills, capsules, granules or tablets.
- the pharmaceutical composition of the present invention can be applied in any dosage form containing the peptide of the present invention as an active ingredient, and can be prepared as an oral or parenteral dosage form.
- Specific dosage forms include oral, rectal, nasal, topical (including buccal and sublingual), subcutaneous, vaginal or parenteral (intramuscular, subcutaneous and intravenous). It may include a suitable form for administration or a form suitable for administration by inhalation, injection or application, but is not necessarily limited thereto.
- the pharmaceutical composition of the present invention is administered in a pharmaceutically effective amount.
- the effective dose level depends on the patient's disease type, severity, drug activity, drug sensitivity, administration time, administration route and excretion rate, duration of treatment, factors including concomitant drugs, and other factors well known in the medical field. can be decided.
- the pharmaceutical composition of the present invention may be administered as an individual therapeutic agent or may be administered in combination with other therapeutic agents, may be administered sequentially or simultaneously with conventional therapeutic agents, and may be administered single or multiple. In consideration of all of the above factors, it is important to administer an amount that can obtain the maximum effect with a minimum amount without side effects, which can be easily determined by those skilled in the art.
- the dosage of the pharmaceutical composition of the present invention varies greatly depending on the patient's weight, age, sex, health status, diet, administration time, administration method, excretion rate and severity of disease, etc., and the appropriate dosage is, for example, It may vary depending on the amount of drug accumulated in the patient's body and/or the specific efficacy of the peptide of the present invention to be used.
- the composition can be calculated based on the EC50 measured to be effective in an in vivo animal model and in vitro, for example, it can be 0.01 ⁇ g to 1 g per 1 kg of body weight, daily, weekly, In a monthly or annual unit period, it may be administered once to several times per unit period, or may be administered continuously for a long period of time using an infusion pump. The number of repeated administrations is determined in consideration of the time the drug stays in the body, the concentration of the drug in the body, and the like. According to the course of disease treatment, the composition may be administered for relapse even after treatment has been completed.
- the pharmaceutical composition of the present invention may further contain at least one active ingredient exhibiting the same or similar function in relation to the improvement and treatment of the disease, or a compound that maintains/increases solubility and/or absorption of the active ingredient.
- a chemotherapeutic agent, an anti-inflammatory agent, an antiviral agent, and/or an immunomodulatory agent may be further included.
- compositions of the present invention may be formulated using methods known in the art to provide rapid, sustained or delayed release of the active ingredient after administration to a mammal.
- Formulations may be in the form of powders, granules, tablets, emulsions, syrups, aerosols, soft or hard gelatin capsules, sterile injectable solutions, or sterile powders.
- the peptides used in the present invention were synthesized by a solid phase method using Fmoc (9-fluorenylmethoxycarbonyl) as a protecting group of N ⁇ -amino acid (Fmoc Solid Phase Peptide Synthesis), and HOBt-DIC (N-hydroxybenzotriazole-diisopropylcarbodiimide) method was used. Peptide extension was followed (Wang C. Chan, Perter D. white, "Fmoc solid phase peptide synthesis” Oxford).
- the synthesized peptide was purified using high-performance liquid chromatography (Prep-HPLC, column C18, 10um, 250mm X 22mm) and lyophilized to obtain a powder form, liquid chromatography mass spectrometry (LC/MS) The molecular weights of the compounds of Table 1 were confirmed. A more detailed synthesis process is described below.
- Rink Amide AM Resin (1mmol, 1.43g) and piperidine 20% containing 50ml of dimethylformamide (N,N-DimethylFormamide, DMF) were put into a 50ml reaction vessel and reacted at room temperature for 10 minutes. . The reaction solution was removed by filtration and washed sequentially with 50 ml of dichloromethane (DCM), methyl alcohol, dichloromethane, and dimethylformamide, respectively.
- DCM dichloromethane
- the reaction solution was removed by filtration, and the synthesized resin was sequentially washed with 50 ml of dichloromethane, methyl alcohol, dichloromethane, and dimethylformamide.
- the compound 1d was quantitatively obtained in the form of a solid phase by vacuum drying.
- Fmoc-Gly-OH (Fmoc-Glycine) (8 mmol, 2.38 g), HOBt (8 mmol, 1.081 g) and DIC (8 mmol, 1.24 mL) were added to the product from which Fmoc was removed in solid form by vacuum drying 50 ml of dimethyl It was added by dissolving in formamide and reacted at room temperature for 4 hours. The reaction solution was removed by filtration, and the synthesized resin was sequentially washed using 50 ml of dichloromethane, methyl alcohol, dichloromethane, and dimethylformamide, respectively. The compound 2a was quantitatively obtained in the form of a solid phase by vacuum drying.
- Rink Amide AM Resin (1mmol, 1.43g) and piperidine (piperidine) containing 20% of dimethylformamide (N,N-Dimethylformamide, DMF) 50ml into a 50ml reaction vessel, and reacted at room temperature for 10 minutes. .
- the reaction solution was removed by filtration and washed sequentially with 50 ml of dichloromethane (DCM), methyl alcohol, dichloromethane, and dimethylformamide, respectively.
- DCM dichloromethane
- the solid product was collected using a centrifuge, washed twice with 500 ml of diethyl ether and dried.
- the obtained solid product was purified using Prep-HPLC (column C18, 10 ⁇ m, 250mm X 22mm), and then lyophilized to obtain each peptide.
- BG is butylene glycol and PG is propylene glycol.
- each cell was seeded into 5 ⁇ 10 4 cells per well in a 24-well plate and cultured for 24 hours in each cell culture condition. The medium was discarded, washed with PBS, and then replaced with a new medium not containing 10% FBS, treated with peptides for each concentration, and incubated for 24 hours. After carefully removing the medium and washing with PBS, MTT reagent was added according to the manufacturer's method, and after reacting at room temperature for 30 minutes, absorbance was measured at 450 nm to confirm that there was no toxicity by each peptide in all cell lines (FIG. 2).
- the mouse adipocyte line 3T3-L1 was treated with each peptide at a concentration of 10 ⁇ M and cultured for 24 hours, then the cells were obtained, the protein was extracted, and the effect on AMPK phosphorylation, which is responsible for the main sub-signaling of adiponectin, was compared and confirmed by Western blot (Fig. 4). It was confirmed that the peptides of the present invention increase phosphorylation of AMPK (V: DMSO, p5: GLYYF)
- a biopsy was performed 24 hours later, and the expression of adiponectin, matrix protein procollagen and p-AMPK was observed using Western blot and immunochemical staining.
- Adiponectin, procollagen and p-AMPK expression were increased in the peptide of the present invention compared to the negative control (vehicle) and the existing P5 peptide ( FIGS. 5 to 7 ).
- the liver cancer cell line HepG2 cells were treated with 1 mM free fatty acid (FFA) and 10 ⁇ M of peptide to compare the triglyceride content.
- FFA free fatty acid
- the fat accumulation inhibitory ability of the peptide of the present invention was superior to that of rosiglitazone and P5, which are positive controls ( Fig. 8).
- ACC acetyl-CoA carboxylase
- AMPK a sub-signal regulator of adiponectin responsible for its regulation were increased (p-ACC is inactive and inhibits triglyceride synthesis).
- the expression of adiponectin and P-AMPK increased after application, and the expression of TRPV1 was decreased.
- the expression of adiponectin increased statistically and significantly more than 4 times compared to before application.
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Abstract
Description
펩타이드 | 분자량 |
LYYF-NH2 | 603.71 |
GLYYF-NH2 | 660.76 |
lYYF | 604.69 |
LyYF | 604.69 |
LYyF | 604.69 |
LYYf | 604.69 |
GlYYF | 661.74 |
GLyYF | 661.74 |
GLYyF | 661.74 |
GLYYf | 661.74 |
lYYF-NH2 | 603.71 |
LyYF-NH2 | 603.71 |
LYyF-NH2 | 603.71 |
LYYf-NH2 | 603.71 |
GlYYF-NH2 | 660.76 |
GLyYF-NH2 | 660.76 |
GLYyF-NH2 | 660.76 |
GLYYf-NH2 | 660.76 |
펩타이드 | 반응물질 |
LYYF-NH2 | 화합물 1d |
GLYYF-NH2 | 화합물 2a |
lYYF | 화합물 3d |
LyYF | 화합물4b |
LYyF | 화합물 5c |
LYYf | 화합물 6d |
GlYYF | 화합물 7a |
GLyYF | 화합물 8a |
GLYyF | 화합물 9a |
GLYYf | 화합물 10a |
lYYF-NH2 | 화합물 11a |
LyYF-NH2 | 화합물 12b |
LYyF-NH2 | 화합물 13c |
LYYf-NH2 | 화합물 14d |
GlYYF-NH2 | 화합물 15a |
GLyYF-NH2 | 화합물 16a |
GLYyF-NH2 | 화합물 17a |
GLYYf-NH2 | 화합물 18a |
Claims (9)
- 서열번호 1 또는 2의 아미노산 서열로 이루어지고, C-말단에 아미노기를 갖는 펩타이드.
- 청구항 1에 있어서, 적어도 하나의 아미노산이 D-형인 펩타이드.
- 청구항 1에 있어서, 하나의 아미노산이 D-형인 펩타이드.
- 서열번호 1 또는 2의 아미노산 서열로 이루어지고, 적어도 하나의 아미노산이 D-형인 펩타이드.
- 청구항 4에 있어서, 하나의 아미노산이 D-형인 펩타이드.
- 청구항 1 내지 5 중 어느 한 항의 펩타이드를 포함하는 화장료 조성물.
- 청구항 6에 있어서, 피부 주름 개선, 민감성 피부 개선, 피부염 개선 또는 발모 촉진용인, 화장료 조성물.
- 청구항 1 내지 5 중 어느 한 항의 펩타이드를 포함하는 피부 주름 개선, 피부염 개선 또는 발모 촉진용 약학 조성물.
- 청구항 1 내지 5 중 어느 한 항의 펩타이드를 포함하는 대사성 질환 치료용 약학 조성물.
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US18/024,819 US20230365643A1 (en) | 2020-09-04 | 2021-08-26 | Peptide, and cosmetic composition and pharmaceutical composition comprising same |
JP2023514969A JP2023541136A (ja) | 2020-09-04 | 2021-08-26 | ペプチド並びにそれを含む化粧料組成物及び薬学組成物 |
CN202180073850.2A CN116457365A (zh) | 2020-09-04 | 2021-08-26 | 肽以及包含所述肽的化妆品组合物和药物组合物 |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101306643B1 (ko) * | 2005-02-09 | 2013-09-12 | 헬릭스 바이오메딕스, 인코포레이티드 | 항미생물성 헥사펩티드 |
JP2016540825A (ja) * | 2013-09-17 | 2016-12-28 | ケーエヌユー−インダストリー コーポレーション ファウンデーション | アディポネクチンに由来するペプチドを含む組成物 |
WO2017213456A2 (ko) * | 2016-06-09 | 2017-12-14 | 주식회사 루비크라운 | 멜라닌 생성 억제 활성을 갖는 펩타이드와 이를 포함하는 조성물 |
KR101967630B1 (ko) * | 2017-03-03 | 2019-04-11 | 서울대학교병원 | 아디포넥틴 유래 펩티드 및 이를 포함하는 피부노화 방지 또는 피부주름 개선용 조성물 |
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KR102611274B1 (ko) * | 2017-05-11 | 2023-12-07 | 킹 압둘라 유니버시티 오브 사이언스 앤드 테크놀로지 | 조직 가공 및 바이오프린팅 시 사용하기 위한 겔을 형성할 수 있는 펩타이드 |
WO2020050427A1 (ko) * | 2018-09-03 | 2020-03-12 | (주)정진호이펙트 | 아디포넥틴 유래 펩티드 및 이를 포함하는 피부노화 방지 또는 피부주름 개선용 조성물 |
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR101306643B1 (ko) * | 2005-02-09 | 2013-09-12 | 헬릭스 바이오메딕스, 인코포레이티드 | 항미생물성 헥사펩티드 |
JP2016540825A (ja) * | 2013-09-17 | 2016-12-28 | ケーエヌユー−インダストリー コーポレーション ファウンデーション | アディポネクチンに由来するペプチドを含む組成物 |
WO2017213456A2 (ko) * | 2016-06-09 | 2017-12-14 | 주식회사 루비크라운 | 멜라닌 생성 억제 활성을 갖는 펩타이드와 이를 포함하는 조성물 |
KR101967630B1 (ko) * | 2017-03-03 | 2019-04-11 | 서울대학교병원 | 아디포넥틴 유래 펩티드 및 이를 포함하는 피부노화 방지 또는 피부주름 개선용 조성물 |
Non-Patent Citations (3)
Title |
---|
CONTACT DERMATITIS, vol. 62, 2010, pages 137 - 49 |
MANABE TAKAYUKI, KAWASAKI KIYOSHI: "D-form KLKLLLLLKLK-NH2 peptide exerts higher antimicrobial properties than its L-form counterpart via an association with bacterial cell wall components", SCIENTIFIC REPORTS, NATURE PUBLISHING GROUP, US, vol. 7, no. 1, 1 March 2017 (2017-03-01), US , pages 1 - 10, XP055907466, ISSN: 2045-2322, DOI: 10.1038/srep43384 * |
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