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Method for correction of total blood serum baee-esterase activity using soya protein isolate |
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IPC classes for russian patent Method for correction of total blood serum baee-esterase activity using soya protein isolate (RU 2509568):
Prodrugs of nonsteroid anti-inflammatory agents (nsaia) with very high speed of penetration through skin and membranes, and new medical applications of above said prodrugs / 2509076
Invention refers to new positively charged NSAIA prodrugs of a common formula (1, 2a, 2b, 2c or 2d) of "1, 2a, 2b, 2c or 2d structure"
Biological materials and their use / 2508296
Peptide of DGSVVVNKVSELPAGHGLNVNTLSYGDLAAD structure is used for suppression of allergic inflammation of respiratory passages, for prophylaxis and treatment of arthritis, as well as for pain relief. A peptide is effective as an adjuvant and for stimulation of IL-12 products in a cell.
Injection composition of polydeoxyribonucleotides for treating osteoarticular diseases / 2508115
What is described is a pharmaceutical composition of polydeoxyribonucleotides extracted from natural sources. The composition contains a fraction of polydeoxyribonucleotides extracted from fish sperm cells, wherein the above polydeoxyribonucleotides possess polymer chains of various molecular weights 70 kDa to 240 kDa.
Boron-based small molecules as anti-inflammatory drugs / 2508113
Present group of inventions refers to medicine, namely to therapy and dermatology, and concerns using boron-based small molecules as anti-inflammatory drugs. That is ensured by administering boron-based small molecules having a specific chemical composition in the effective amount.
Positive allosteric modulators of m1 receptors based on pyranyl aryl methylbenzoquinazolinone / 2507204
Invention relates to novel pyranyl aryl methylbenzoquinazolinone compounds of formula (I), which are positive allosteric modulators of the M1 receptor and which can be used to treat diseases associated with the M1 receptor, such as Alzheimer's disease, schizophrenia, pain disorders or sleep disturbance. In formula (I) X-Y are selected from a group comprising (1) -O-CRARB-, (2) -CRARB-O-, (3) -CRARB-SRC-, (4) -CRARB-NRC- and (5) -NRC-CRARB-, where each RA and RB is a hydrogen atom, and RC is selected from a group comprising (a) hydrogen, (b) -C(=O)-C1-6alkyl, (c) -C1-6alkyl, (d) -C(=O)-CH2-C6H5, (e) -S(=O)2-C1-6 alkyl, R1 is a hydroxy group, R2 is selected from a group comprising (1) -phenyl, (2) - heteroaryl, where the phenyl or heteroaryl group R2 is optionally substituted; the rest of the values of the radicals are given in the claim.
Novel phenylpyrazinones as kinase inhibitors / 2507202
Present invention relates to organic chemistry and specifically to 5-phenyl-1H-pyrazin-2-one derivatives of general formula II or pharmaceutically acceptable salts thereof, where R denotes -R1 or - R1-R2-R3; R1 denotes aryl or heteroaryl, and is optionally substituted with one or two R1'; where each R1' independently denotes C1-6alkyl, halogen or C1-6halogenalkyl; R2 denotes -C(=O), -CH2-; R3 denotes R4; where R4 denotes an amino group or heterocycloalkyl, and is optionally substituted with one or two substitutes selected from C1-6alkyl, hydroxy group, oxo group, C1-6hydroxyalkyl, C1-6alkoxy group; Q denotes CH2; Y1 denotes C1-6alkyl; Y2 denotes Y2b; where Y2b denotes C1-6alkyl, optionally substituted with one Y2b'; where Y2b' denotes a hydroxy group, n and m are equal to 0; Y4 denotes Y4c or Y4d; where Y4c denotes lower cycloalkyl, optionally substituted with halogen; and Y4d denotes an amino group, optionally substituted with one or more C1-6alkyl; where "aryl" denotes phenyl or naphthyl, "heteroaryl" denotes a monocyclic or bicyclic radical containing 5 to 9 atoms in the ring, which contains at least one aromatic ring containing 5 to 6 atoms in the ring, with one or two N or O heteroatoms, wherein the remaining atoms in the ring are carbon atoms, under the condition that the binding point of the heteroaryl radical is in the aromatic ring, "heterocycloalkyl" denotes a monovalent saturated cyclic radical consisting of one ring containing 5 to 6 atoms in the ring, with one or two ring heteroatoms selected from N, O or SO2. The invention also relates to use of the compound of formula II or a pharmaceutical composition based on the compound of formula II.
Alpha-substituted omega-3 lipids, activators or modulators of peroxisome proliferator activated receptor (ppar) / 2507193
Invention relates to novel omega-3 lipid compounds of general formula (I) or to their pharmaceutically acceptable salt, where in formula (I): R1 and R2 are similar or different and can be selected from group of substitutes, consisting of hydrogen atom, hydroxy group, C1-C7alkyl group, halogen atom, C1-C7alkoxy group, C1-C7alkylthio group, C1-C7alkoxycarbonyl group, carboxy group, aminogroup and C1-C7alkylamino group; X represents carboxylic acid or its carbonate, selected from ethylcarboxylate, methylcarboxylate, n-propylcarboxylate, isopropylcarboxylate, n-butylcarboxylate, sec-butylcarboxylate or n-hexylcarboxylate, carboxylic acid in form of triglyceride, diglyceride, 1-monoglyceride or 2-monoglyceride, or carboxamide, selected from primary carboxamide, N-methylcarboxamide, N,N-dimethylcarboxamide, N-ethylcarboxamide or N,N-diethylcarboxamide; and Y stands for C16-C22 alkene with two or more double bonds, which have E- and/or Z-configuration.
Pharmaceutical composition containing physiologically active heptapeptides, having antispasmodic, anxiolytic, central anti-inflammatory and analgesic activity, as well as anti-alcohol activity / 2506269
Disclosed is use of a heptapeptide of general formula Tyr-D-Ala-Phe-Gly-Tyr-X-Ser-NH2, where X is D-Pro or Dh-Pro, or Dh-D-Pro, where Dh-Pro is 3,4-dehydroproline, as an antispasmodic, anxiolytic, central anti-inflammatory or anti-alcohol agent.
Agent having hypoglycemic and anti-inflammatory activity / 2506091
Invention refers to pharmaceutical industry, namely an agent having hypoglycemic and anti-inflammatory activity. The agent having hypoglycemic and anti-inflammatory activity is prepared by extraction of a herbal material consisting of a mixture of ground common burdock roots and rhizomes; common dandelion roots; horseheal roots and rhizomes; bean shoots; bilberry shoots; cinquefoil shoots and common nettle leaves in 40% ethanol in the certain environment; the combined extracts are filtered, evaporated, purified by separation, dried and ground.
2-(3-hydroxy-4-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2h-chromen-4,8-diol as analgesic agent / 2506079
Invention refers to pharmaceutics and medicine and concerns using 2-(3-hydroxy-4-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromen-4,8-diol of formula 1 as an analgesic agent.
Method for preparing cake shelf fungus extract / 2509567
Invention refers to pharmaceutical, food and cosmetic industry and concerns preparing a cake shelf fungus extract. The method for preparing the cake shelf fungus extract involving freezing cake shelf fungus, wetting it with a water solution containing dimethyl sulphoxide and sodium hydroxide, with a solution temperature being 50-90°C, and keeping at the above temperature for 1-2 hours.
Compositions of borinic acid / 2509553
Invention refers to pharmaceutical industry and represents an oral care composition having pH min. 8 or buffered so that to maintain the pH value min. 7, containing 3- hydroxypyridine-2-carbonyloxy-bis-(3-chlor-4-methylphenyl)borane in a combination or together with an orally acceptable carrier.
Composition applicable as personal hygiene product and methods for using it / 2509552
Invention refers to cosmetology and represents a composition applicable by a user as a personal hygiene product in the form of a bath or shower gel, containing: (a) no more than 11.5 wt % of an anionic surfactant representing alkyl sulphate, alkyl sarcosinate, or any combination thereof; (b) no more than 3 wt % of a zwitterionic surfactant representing fatty acid amidoalkylbetaine, (c) not less than 0.1 wt % of a hydroxyalkylcellulose derivative with a long-chain alkyl group; and (d) water.
Method of human health improvement / 2509547
Invention refers to medicine, namely recreation therapy, and may be used for human health improvement. That is ensured by traditional medical examination of the patient. The findings are used to draw up the rehabilitation program including body cleansing, intestine and liver purification, physical exercises. One week before the beginning of the rehabilitation program, the patient starts separate nutrition with preferential vegetable food and dairy products, limited consumption of salt, alcohol and sugar. One day before the rehabilitation program, a fasting day is kept with taking 1% kephir or fresh apple juice. Further, on the first two days of the three-day program or on the first four days of the seven-day program, the body is cleansed by keeping a juice diet. The juice diet contains fresh vegetable and fruit juices, herbal infusions and mineral water. Water is unlimited. On the first day of the cleansing program, the intestine is purified with the preparation Fortrans. Starting from the first day the liver and gall bladder are cleansed with using herbal and saline choleretics for four days of the 7-day program and for two days of the 3-day program. That is combined with paradoxical respiration by Strelnikova's technique and hydrotherapy. Physical exercises involve physical loads on a cardio-vascular machine, one training as prescribed by the doctor - yoga, pilates, chi gong, water aerobics or hypoxi capsule. Therapeutic massage and lymph drainage massage follow. Then body-detox, ozone therapy, collagenarium procedures are performed. Cold training procedures involve Linear Kneipp, saunas, swimming pool, turpentine bathes. Bathing and cold training procedures are followed by pilling and algae wraps. From the 5th day of the 7-day program, or from the 3rd day of the 3-day program, the diet involves water cereals, vegetable and fruit salads, vegetable fast soups.
Adhesive ointment for treating oral mucosal involvements in lichen acuminatus / 2508120
Invention refers to pharmaceutical industry, namely to an agent for treating an oral mucosal involvement accompanying lichen acuminatus. An adhesive ointment for treating the oral mucosal involvements accompanying lichen acuminatus containing sea buckthorn oil and 0.5% prednisolone ointment, socoseryl dental adhesive paste and vitamin A in the specific proportions.
Herbal trematocidal drug for excysted larvae fasciola hepatica / 2508119
Invention refers to pharmaceutical industry, particularly to using common dandelion herb as a trematocidal drug for excysted larvae Fasciola hepatica.
Method for increasing radioresistance in mice / 2508118
Invention refers to pharmaceutical industry, particularly to a method for increasing the radioresistance in mice. The method for increasing the radioresistance in mice consisting in the fact that 20-30 min before a radiation exposure, parsley juice diluted with normal saline is introduced intramuscularly.
Hair styling composition / 2508088
Present invention refers to cosmetology, particularly represents a hair styling composition containing a dispersion of at least one polyurethane that can be prepared by a reaction of one or more water-insoluble, water-nondispersible polyurethane pre-polymers with isocyanate functional groups with one or more compounds containing aminofunctional groups and specified in primary and/or secondary amines, and/or diamines.
Method for preparing agent for making 99m tc norfloxacin / 2506954
Invention refers to a method for preparing an agent for making 99m Tc Norfloxacin. The above method involves preparing tin (II) chloride dihydrate to be mixed with a norfloxacin hydrochloride powder, freezing the prepared mixture at liquid nitrogen temperature, lyophilising at temperature -50°C in vacuum -0.0015 torr for at least 20.5 hours and drying additionally for at least 5.5 hours at temperature +16±2°C.
Method for preparing biologically active complex of powdered young sprouts of sea buckthorn / 2506953
Invention refers to pharmaceutical industry, namely a method for preparing a biologically active complex containing serotonin. The method for preparing the biologically active complex containing serotonin involves milling a herbal raw material that is young sprouts of sea buckthorn collected in the early spring and containing 0.9%-1.1% of serotonin in a cutting mill; mixing the milled herbal raw material and ascorbic acid in a blade mixer; carrying out solid-phase mechanochemical treatment in a roll mill in the intensive mechanical environment in the presence of solid edible agents specified in: citric acid - sodium chloride at a dry substance (1:0.5)-(1:1), or acid, alkaline and phosphate-containing agents to prepare a fine powder at particle size 125 mcm.
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FIELD: medicine. SUBSTANCE: method refers to preventive medicine and concerns decreasing total BAEE-esterase activity. For this purpose, soya protein isolate 30 gram has been daily introduced into the subjects for 2 months. EFFECT: decreasing the BAEE-esterase activity of protein-degrading enzymes can be used to prevent inflammatory processes. 1 ex, 1 tbl
The method relates to the field of preventive medicine and can be used as an additional means for correcting baee-esterase activity to reduce the risk of inflammatory processes. In the development of pathological conditions involving inflammation involves all types of proteolytic enzymes [2]. Proteolytic enzymes serine has baea-esterase activity, which is increased in inflammatory processes in the body. It is known that inhibitors of soybean reduce the activity of some proteolytic enzymes [4]. It is established that soy products are used as a means of diet and dataprotection of several diseases [1]. Soybean protein can be absorbed into the bloodstream through the gastrointestinal tract [5]. The method of regulation baee-esterase activity of proteolytic enzymes in the body through intake of soy protein isolate. The technical result of the present invention is the use of soy protein isolate for correction baee-esterase activity of blood serum that can serve as a prevention of inflammatory diseases. The method does not require expensive, special treatment, systematic control. The method is as follows. Within 2 months of egene is but a group of healthy people ate soy protein isolate, with antiproteolytic activity, in the amount of 30 grams per day. As a result, the level baee-esterase activity of serum significantly decreased by 20%. Isolate soy protein is myopically powder without taste and does not require special preparation before use. Isolate enough to mix with water or fruit juice. Example The study was conducted on 30 healthy men and women aged 35-60 years. The participants received daily 30 g of soy protein isolate. A blood examination was taken from the cubital vein in the morning on an empty stomach before the study and after 2 months of taking soy protein isolate. In serum measured total bee-asterisknow activity of proteolytic enzymes [3]. Table 1 presents the results of reception of soy protein isolate for 2 months, reflecting a significant decrease baee-esterase activity of blood serum 20% (p<0,05): before receiving this activity was 0,343±0,010, and after receiving 0,282±0,008.
Thus, the increase baee-esterase activity of blood serum via reception isolate soy protein appears to be reliable and can be used to correct the overall level baee-esterase activity in the body in inflammatory processes. Literature 1. Borodin E.A., T. Aksenova, Anishchenko NI Food products from soybeans. A new role // Vestnik DVO ran. 2000. No. 5. P.72-85. 2. Drakan E.A., Baluevsky and THUS al. Study the expression of cathepsins D and L in the process of oncogenic transformation of fibroblasts. Questions of medical chemistry, 1994. No. 3. T. C.2-6. 3. Ogloblin OG, Maliyev BM Activity of proteases of granulocytes and their kislotostabilen inhibitors in bronchial secretions of patients with newly diagnosed pulmonary tuberculosis, complicated by nonspecific bronchitis // Problems of tuberculosis. 1983. No. 2. Pp.33-37. 4. J.N. Losso The biochemical and functional food properties of the bowman-birk inhibitor. Crit Rev Food Sci Nutr. 2008 Jan; 48(1):94-118. 5. Kennedy A.R. Chemopreventive agents: protease inhibitors // Pharmacol. Ther. 1998. V.78, Issue.3. P.167-209. The way to reduce bee-esterase activity of the blood serum, which consists in the fact that healthy people over 2 months of daily use 30 grams of soy protein isolate.
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