159results about How to "Increase excretion" patented technology

Expression systems are disclosed for the direct expression of peptide products into the culture media where genetically engineered host cells are grown. High yield was achieved with novel vectors, a special selection of hosts, and / or fermentation processes which include careful control of cell growth rate, and use of an inducer during growth phase. Special vectors are provided which include control regions having multiple promoters linked operably with coding regions encoding a signal peptide upstream from a coding region encoding the peptide of interest. Multiple transcription cassettes are also used to increase yield. The production of amidated peptides using the expression systems is also disclosed.

There is provided a 5-thio-β-D-glucopyranoside compound of the following formula, which has an inhibitory effect on SGLT2 activity, or a pharmaceutically acceptable salt thereof or a hydrate thereof. There is also provided a pharmaceutical preparation, particularly a prophylactic or therapeutic agent for diabetes, diabetes-related diseases or diabetic complications, which comprises such a compound as an active ingredient.

The invention discloses mask liquid with multiple skin care effects and a preparation method thereof, aims at providing mask liquid which has effects of skin whitening, speckle removing, wrinkle smoothing, inflammation relieving and diminishing, long-lasting moisturizing and grease balancing, and belongs to the technical field of cosmetics. According to the technical scheme, the mask liquid is prepared from, by weight, 0.5%-3% of sericin, 3.011%-14.02% of a plant extract, 1.11%-8.35% of a moisturizer, 8%-15% of polyalcohol, 0.1%-1.5% of active peptides, 0.08%-0.15% of Carbomer, 0.08%-0.15% of triethanolamine, 0.02%-0.06% of disodium EDTA, 0.3%-0.5% of a preservative and the balance deionized water.

Expression systems are disclosed for the direct expression of peptide products into the culture media where genetically engineered host cells are grown. High yield was achieved with novel vectors, a special selection of hosts, and / or fermentation processes which include careful control of cell growth rate, and use of an inducer during growth phase. Special vectors are provided which include control regions having multiple promoters linked operably with coding regions encoding a signal peptide upstream from a coding region encoding the peptide of interest. Multiple transcription cassettes are also used to increase yield. The production of amidated peptides using the expression systems is also disclosed.

A Chinese medicine for preventing and treating cholecystitis, cholelithiasis and the inflammation of biliary tract, and improving the function of gallbladder and liver is prepared from 23 Chinese-medicinal materials including tackahoe, capejasmine fruit, white peony root, cyprus tuber, etc.

There is provided a heteroaryl 5-thio-β-D-glucopyranoside compound of the following formula, which has an inhibitory effect on SGLT2 activity, or a pharmaceutically acceptable salt thereof or a hydrate thereof. There is also provided a pharmaceutical preparation, particularly a prophylactic or therapeutic agent for diabetes, diabetes-related diseases or diabetic complications, which comprises such a compound as an active ingredient.

This invention relates to a process of synthesis and composition of open chain (ring), closed ring, linear branched and or substituted polyamines, polyamine derived tyrosine phosphatase inhibitors and PPAR partial agonists / partial antagonists via a series of substitution reactions and optimizing the bioavailability and biological activities of the compounds. Polyamines prevent the toxicty of neutoxins and diabetogenic toxins including paraquat, methyphenyl pyridine radical, rotenone, diazoxide, streptozotocin and alloxan. These polyamines can be to treat neurological, cardiovascular, endocrine acquired and inherited mitochondrial DNA damage diseases and other disorders in mammalian subjects, and more specifically to the therapy of Parkinson's disease, Alzheimer's disease, Lou Gehrig's disease, Binswanger's disease, Olivopontine Cerebellar Degeneration, Lewy Body disease, Diabetes, Stroke, Atherosclerosis, Myocardial Ischemia, Cardiomyopathy, Nephropathy, Ischemia, Glaucoma, Presbycussis, Cancer, Osteoporosis, Rheumatoid Arthritis, Inflammatory Bowel Disease, Multiple Sclerosis and as Antidotes to Toxin Exposure.

The present invention relates to novel antagonists to a B1-bradykinin (B1-BK) receptor which have a good affinity and selectivity therefor, some of which being at least partially resistant to enzymatic degradation. The synthesis of the B1 receptors is induced during inflammation. Symptoms associated with inflammation (elevated hydrostatic pressure and plasma leakage or extravasation) have been observed in diabetic animal models (streptozotocin-induced diabetes (STZ)) as well as in spontaneously hypertensive rats (SHR). The present inventors confirm the presence of B1-BK receptors in these two models. B1-BK antagonists abolished the vasocontraction induced by B1-BK in SHR and STZ, and reduced the glycemia of diabetic animals to normal levels. The present B1-antagonists are useful for treating any condition wherein B1-receptor is expressed, particularly during inflammation, and more particularly wherein B1-receptor expression results in diabetic vasculopathy, other diabetic symptoms associated with an insulitis and a post-capillary resistance building as a consequence of the presence of a B1-receptor.

The invention discloses Al18F-NOTA-PEG6-TATE of a targeted somatostatin receptor and a preparation method and application of Al18F-NOTA-PEG6-TATE. The preparation method of the label includes the steps that a somatostatin derivative TATE and a difunctional chelating agent NOTA are connected through PEG to generate a radiolabelled precursor, then positron nuclide 18F labeling is carried out through a one-pot method, and the 18F labeled somatostatin derivative Al18F-NOTA-PEG6-TATE can be obtained. The method can be carried out in an acetate buffer solution system or an acetonitrile reaction system, and the method has the advantages of being easy and convenient to operate and high in labeling rate and product purity. The prepared positron label of the targeted somatostatin receptor can be applied to preparation of a PET / CT molecular probe or tumor therapy medicine, and provides a novel thought for synthesis of the clinical PET / CT molecular probe.

The present invention provides a method for preparing an aryl 5-thio-β-D-aldohexopyranoside derivative of Formula (III), which comprises reacting a 5-thio-D-aldohexopyranose derivative of Formula (I) with Ar—OH of Formula (II) in the presence of a phosphine represented by PR11R12R13 and an azo reagent represented by R21—N═N—R22 in accordance with the following scheme.

The present invention comprises methods and compositions for the reduction of oxalate in humans, animals and plants. For example, the invention provides methods and compositions for the delivery of one ore more oxalate-reducing enzymes to the intestinal tracts of persons and animals. The methods and compositions can be used in treating and preventing oxalate-related conditions.

The present invention relates to a method for increasing in a baked product, after baking, the level of water-soluble arabinoxylan with an average degree of polymerization ranging from 5 to 50, preferably ranging from 5 to 35, more preferably ranging from 5 to 25, said method comprising the steps of:—Preparing a dough for a baked product with flour, a mixture of flours or a mixture of flour (s) with milling fractions having a total arabinoxylan content of at least 2.0%, preferably at least 2.5%, and—Adding to said dough an enzyme preparation comprising at least one thermophilic endoxylanase in an amount at least 2-fold higher, preferably at least 3 to 6 times higher or even 10 times higher than the dose conferring 90% of the maximal bread volume increase obtained by addition of such enzyme preparation to the recipe of said baked product. Advantageously with said method baked products can be obtained that have a level of arabinoxylan of the desired type of at least 1.7%, more preferably at least 1.75%, such as at least 1.8%, 1.9% or 2.0%. The present invention further relates to baked products obtainable by this method, and to an improver and a dough which may be used for the preparation of such products. Baked products according to the invention advantageously have improved health benefits.

The invention discloses an application of hydroxyacetophenone and its derivatives in preparing drugs for curing cholelithiasis, which can enhance the excretion of bile and lower down the content of cholesterin and bilirubin in the bile, thus realizing the dual effects of bile expelling and lithiasis resolving. Therefore, the invention can be applied to treat lithiasis.

The invention discloses a color-protecting and fresh-keeping method for fresh-cut potatoes. The method includes selecting fresh or stored potatoes as the raw material, washing cleanly, peeling, cutting into chips with thicknesses of 0.5-1.0mm, adding a composite color-protecting fresh-keeping solution having the same mass with the potato chips, and soaking for 10-30min at 20 DEG C-30 DEG C; then fishing out the potato chips from the composite color-protecting fresh-keeping solution, washing cleanly with water, soaking in water at 10-150w ultrasonic power and 10-50kHz ultrasonic frequency for 10-30min of ultrasonic time; fishing out the potato chips and draining off, processing for 10-30min under the condition of subzero 0.01MPa-subzero 0.09MPa of vacuum degree; and finally taking the potato chips out of the vacuum environment and soaking immediately into an arbutin solution with the concentration of 0.05-0.3mmol / L, soaking for 5-15min, taking the soaked potato chips out and draining for 1-3min, performing decompression packaging immediately, and storing at an environment of subzero 4 DEG C to zero DEGC. The method adopts ultrasonic and vacuum cooperative processing as well as the Chinese herb extract arbutin as the color-protecting fresh-keeping agent to inhibit enzyme and microbial activities, is better in effect compared with the prior art, and ensures that various potato processed products are prevented from brown stain in a cold storage process for more than 10 days.

A compound represented by the formula: wherein Ar represents a group represented by the formula: (wherein Y represents methylene or an oxygen atom, R1 represents aminosulfonyl, C1-6 alkylaminosulfonyl, C1-6 alkylcarbonylamino or C1-6 alkylsulfonylamino, R2 represents a hydrogen atom or C1-6 alkyl, R3 represents C1-6 alkyl, and R4 represents a hydrogen atom or C1-6 alkyl); X represents a carbonyl group, or a methylene group which may be substituted with a hydroxy group; and L represents an optionally substituted C4-5 alkylene group, or a salt thereof is provided.

A method of producing bronchorelaxation in the lungs of a human or animal affected by airway obstruction comprises administration of a pharmacologically effective amount to the body or to the intestine of said human or animal of an agent capable of binding mercury in elemental, ionic and / or organic form present in the body or in the intestinal lumen to enhance its excretion via the feces and / or the urine. A corresponding use of the agent and its use for the manufacture of a medicament are also disclosed.

The invention discloses a traditional Chinese medicine composition, in particular discloses a traditional Chinese medicine composition for treating prostatic hypertrophy and a preparation method thereof. The traditional Chinese medicine composition for treating prostatic hypertrophy is characterized by being prepared from the following components: Radix scutellariae, phellodendron bark, oldenlandia, tuckahoe, rhizoma alismatis, rhizoma anemarrhenae, safflower, raspberry, self-heal, houttuynia, rough gentian, dried rehmannia root, yam rhizome, chuanxiong rhizome, angelica, morinda root, broomrape, moutan bark, gardenia, red peony root, dandelion, lysimachia, coix seed, prepared aconite root, radix linderae, cassia, rhubarb, bitter cardamon, turtle shell, centipede, bombyx batryticatus, oyster, pangolin, antler, mastic, myrrh and menthol. The traditional Chinese medicine composition prepared by the invention can be used for clearing away heat to purge pathogenic fire, removing dampness to reduce phlegm, promoting blood circulation to diminish inflammation, nourishing the kidney to replenish essence, nourishing the kidney to reduce urination, softening hardness to dissipate stagnation and dissipating blood stasis to remove stagnation, and can improve the immunity of human bodies, improve the arterial blood flow and dilate vessel walls. By using the traditional Chinese medicine composition for treating 920 cases, the total effective rate reaches 96%.

This document provides natriuretic polypeptides. For example, this document provides polypeptides having a natriuretic activity. In some cases, a polypeptide provided herein can have natriuretic activities without inducing excessive hypotension. This document also provides methods and materials for inducing natriuretic activities within a mammal.

The invention relates to the field of commodities, specifically to a moisture-retaining whitening face cream. The moisture-retaining whitening face cream comprises the following substances by weight: 5 to 8 parts of glycerin, 3 to 5 parts of aloe essence, 5 to 8 parts of green tea seed oil, 8 to 15 parts of pearl powder, 3 to 5 parts of vitamin E acetate, 2 to 5 parts of lecithin wax, 5 to 8 parts of candelilla wax, 8 to 15 parts of refined shea butter, 8 to 20 parts of refined coconut oil, 3 to 8 parts of vitamin B, 1 to 5 parts of stearoxyl trimethyl silane, 3 to 15 parts of hyaluronic acid, 5 to 15 parts of micro walnut powder, 5 to 8 parts of alga extract, 8 to 15 parts of molecular distillation monostearin, 10 to 15 parts of olive oil, 3 to 8 parts of arbutin and 3 to 8 parts of squalane. The moisture-retaining whitening face cream provided by the invention is rich in abundant vitamins, protein and collagen, can effectively retain moisture, supplement water and soften cutin, and is capable of promoting metabolism, activating skin cells, improving blood circulation and accelerating melanin decomposition and excretion, thereby reducing deposition skin pigment and whitening the skin.

The present invention relates to multimeric (e.g., dimeric, trimeric) forms of peptide vectors that are capable of crossing the blood-brain barrier (BBB) or efficiently entering particular cell types. These multimeric peptide vectors, when conjugated to agents (e.g., therapeutic agents) are capable of transporting the agents across the BBB or into particular cell types. These compounds are therefore particularly useful in the treatment of neurological diseases.

There is provided a heteroaryl 5-thio-β-D-glucopyranoside compound of the following formula, which has an inhibitory effect on SGLT2 activity, or a pharmaceutically acceptable salt thereof or a hydrate thereof. There is also provided a pharmaceutical preparation, particularly a prophylactic or therapeutic agent for diabetes, diabetes-related diseases or diabetic complications, which comprises such a compound as an active ingredient.

The invention discloses a traditional Chinese medicine formula with effects of removing freckles and whitening and a preparation method thereof and belongs to the technical field of human health careproducts. The traditional Chinese medicine formula contains the following raw materials: 4-18 parts of ganoderma lucidum, 9-36 parts of tricholoma matsutake, 3-12 parts of ginseng, 1-4 parts of bearberry leaf extract, 3-12 parts of rhizoma polygonati, 3-12 parts of bighead atractylodes rhizome, 1-6 parts of bletilla striata, 3-12 parts of white paeony root, 3-12 parts of ampelopsis japonica, 3-12parts of silkworm larva, 4-12 parts of poria cocos, 1-6 parts of angelica sinensis, 3-9 parts of paeonia lactiflora, 3-12 parts of astragalus, 1-5 parts of almond, 2-10 parts of semen coicis, 1-5 parts of fructus kochiae, 1-5 parts of cortex dictamni, 1-5 parts of liquorice and 2-6 parts of mint. The whitening and freckle removing skin care product provided by the invention is mild and non-irritating, can be applicable to population with sensitive skin, is simple and convenient to use, natural and zero in side effect and has excellent application prospects.

The invention provides a special conditioning and nourishing film for use at a genital of a woman. The special conditioning and nourishing film is a product formed by uniformly infiltrating conditioning and nourishing liquid on a non-woven fabric film and packaging the non-woven fabric film, wherein the conditioning and nourishing liquid is prepared from the following ingredients in percentage byweight: 0.5-2% of colorless nano silver solution (with the concentration of 1,000 ppm), 0.5-2% of vitamin E, 1-5% of aloe extract (with 3% solid content), 1-5% of ginseng extract (2.5% solid content), 1-5% angelica extract (3% solid content), 1-5% of lily extract (2.5% solid content), 1-10% of purslane extract (30% solid content), 0.001-0.005% of lauric acid-modified superoxide dismutase (the number of active cells is 4 million units / g), 0.2-1% of sodium carboxymethylcellulose, 0.01-0.1% of glutamic acid, 0.01-0.1% of arginine, 0.01-0.1% of folic acid and the remaining of deionized water; andthe non-woven fabric film is 50-100g / m<2> in gram weight, and is prepared from the following materials in percentage by weight: 50-99.9% of viscose fiber and 0.1-50% of Dacron. The special conditioning and nourishing film provided by the invention has the functions of killing bacteria, diminishing inflammation, contracting vagina, whitening the genital, increasing skin elasticity of the genital and the like.

The present invention features a compound having the formula A-X-B, where A is peptide vector capable of enhancing transport of the compound across the blood-brain barrier or into particular cell types, X is a linker, and B is a GLP-1 agonist (e.g., exendin-4 or an exendin-4 analog). The compounds of the invention can be used to treat any disease where increased GLP-1 activity is desired, for example, metabolic diseases, such as obesity and diabetes.

The invention relates to a preparation method of a spicy bamboo shoot. The spicy bamboo shoot is prepared from the following raw materials by weight: 40-60kg of fresh sweet bamboo shoots, 10-20kg of fresh chillies, 5-10kg of garlic cloves, 0.1-0.5kg of star anise oil, 20-40kg of white wine with 40-60 alcohol by volume, 2-5kg of salt and 1-3kg of sweet tea tender leaves. The preparation method comprises the steps as follows: cutting the fresh sweet bamboo shoots into 2-5cm segments; cutting up chillies, garlic cloves and sweet tea tender leaves; adding star anise oil, white wine and salt; stirring the mixture to be uniform; filling the mixture in a glass container or pottery pot; and sealing the container or pottery pot to reach an airtight effect and preserving for more than ten days, thus obtaining the product. The spicy bamboo shoot has a unique flavor and a good mouthfeel and meets the requirements of people on aroma, spiciness, sour, appetizing, nutrient, tastiness and portability.

The present invention relates to methods and compounds for treating specific early stage aspects and late stage aspects of diabetic nephropathy. Methods and compounds for treating various physiological features associated with early stage and with late stage diabetic nephropathy are also provided.

This document provides natriuretic polypeptides. For example, this document provides polypeptides having a natriuretic activity. In some cases, a polypeptide provided herein can have natriuretic activities without inducing excessive hypotension. This document also provides methods and materials for inducing natriuretic activities within a mammal.

Disclosed herein are parenteral solutions containing 7-halo-1,2,3,4-tetrahydro-3-aryl-6-quinazoline sulfonamide in N,N-dimethylactamide, polyethylene glycol and D5W useful in the treatment of hypertension, heart failure and renal disease leading to edematous states. Also disclosed are methods for preparing such solutions.