摘要:
Novel phenoxyalkyl-carboxylic acid derivatives of the formula
wherein R1 and R2, which may be the same or different, are hydrogen or methyl; N IS 1 OR 2; Z is hydroxyl or alkoxy; and Y is a 5- or 6-membered heterocyclic ring containing, as hetero atoms, 1 or 2 sulfur, oxygen or nitrogen atoms, which heterocyclic ring may be substituted by halogen atoms or lower alkyl, alkoxy or alkoxyalkoxy radicals and may also contain a fused benzene nucleus, which can be substituted by halogen atoms or alkoxy or an alkylene radical; AND THE PHARMOCOLOGICALLY COMPATIBLE SALTS THEREOF, ARE OUTSTANDINGLY EFFECTIVE AS SERUM LIPID DEPRESSANTS AND ARE THUS EFFECTIVE THERAPEUTIC AGENTS IN THE TREATMENT OF ATHEROSCLEROSIS.
摘要翻译:式R1 | Y-CO-NH-(CH2)n -O-C-CO-Z | R2的新型苯氧基烷基 - 羧酸衍生物,其中可以相同或不同的R 1和R 2是氢或甲基; N IS 1 OR 2; Z是羟基或烷氧基; Y为5或6元杂环,杂环为1或2个硫,氧或氮原子,该杂环可被卤素原子或低级烷基,烷氧基或烷氧基烷氧基取代,也可含有 稠合的苯核,其可以被卤素原子或烷氧基或亚烷基取代; 并且其药理学兼容的盐,作为血清脂质沉着剂是非常有效的,并且是有效的治疗药物治疗甲状腺功能亢进症。
摘要:
Creatinine amidohydrolase and creatine amidinohydrolase are prepared by a process comprising culturing a microorganism in a creatinine-containing medium, digesting same, obtaining the creatinine amidohydrolase in substantially pure form from the water-soluble digestion fraction and, optionally separating by ion exchange chromatography any creatine amidinohydrolase present.
摘要:
In the production of tablets which are to undergo disintegration in use wherein the tablet components are mixed and pressed into predetermined shape, the improvement which comprises incorporating into the mix at least one inert readily volatilizable solid adjuvant, pressing the mix into shape, and thereafter volatilizing the adjuvant, whereby the resulting tablets are porous, strong, shape retaining and readily disintegratable. Volatilization can be effected by sublimation or application of vacuum. The adjuvant preferably comprises urethane, urea, ammonium carbonate, ammonium bicarbonate, hexamethylene-tetramine, benzoic acid, phthalic anhydride, naphthalene or camphor present in about 5 to 50 percent, especially about 10 to 30 percent, by weight of the total tablet mix.
摘要:
WHEREIN R1 is lower alkyl substituted by at least one of hydroxyl, alkoxy or acyloxy; or is cycloalkyl or straight-chained or branched lower alkenyl; R2 and R3 are hydrogen, halogen, or nitro or lower alkyl, alkoxy or alkylthio and R4 is hydrogen or acyl; when R4 is acyl, R1 can also be lower alkyl; AND THE PHARMACOLOGICALLY COMPATIBLE SALTS THEREOF; EXHIBITS SHOWN ANTI-LIPOLYTIC, ANTI-HYPERLIPAEMIC AND ANTIHYPERCHOLESTEROLAEMIC ACTION.
New N(6)-disubstituted adenosine coupound of the formula:
摘要:
Uric acid is determined by contacting a sample suspected of containing uric acid with a phosphate buffer, an NADH solution, ethanol, alcohol dehydrogenase and catalase in the presence of air to form a reaction mixture containing 0.3 to 0.7 volume percent alcohol, measuring a first extinction value, adding uricase to the reaction mixture, measuring a second extinction value spectrophotometrically and taking the difference between the extinction values as a measure of the initial uric acid content in the sample.
摘要:
1. IN THE PROCESS OF COATING TABLET CORES OR THE LIKE WITH A COATING COMPRISING PLACING SAID CORES IN A CONTAINER, ROTATING SAID CONTAINER TO MOVE SAID CORES ABOUT, SUPPLYING A SUSPENSION OR SOLUTION OF COATING MATERIAL TO SAID CONTAINER TO COAT SAID CORES AND SUPPLYING A DYRING GAS TO SAID CONTAINER TO DRY THE COATING ON SAID CORES, THE IMPROVEMENT WHICH COMPRISES INTRODUCING SAID DRYING GAS INTO THE BODY OF MOVING TABLET CORES BELOW THE LEVEL THEREOF IN SUCH MANNER THAT A SUBSTANTIALLY TABLET-FREE GAS SPACE IS FORMED JUST BEYOND THE POINT OF DISCHARGE OF SAID GAS, SAID GAS BEING DIRECTED IN THE MAIN DIRECTION OF MOVEMENT OF THE TABLET CORES, SPRAYING OF SAID COATING MATERIAL INTO SAID GAS SPACE TAKING PLACE IN A DIRECTION SUBSTANTIALLY PARALLEL TO THE DIRECTION OF DISCHARGE OF SAID GAS.
摘要:
Storage stable reduced nicotinamide-adenine-dinucleotide (NADH) compositions, which do not form dehydrogenase inhibitors of prolonged time periods, are produced by forming a dilute aqueous solution of inhibitor-free NADH and maintaining this solution in a thin layer vacuum.
WHEREIN R IS AN UNSUBSTITUTED OR SUBSTITUTED PHENYL OR BENZYL RADICAL, THE SUBSTITUENTS BEING HALOGEN ATOMS OR LOWER ALKYL OR ALKOXY RADICALS, E.G., OF FROM 1 TO 6 CARBON ATOMS, AND N IS 1, 2 OR 3; AND THE PHRMACOLOGICALLY COMPATIBLE SALTS THEREOF. HAVE OUTSTANDING ANTI-EDEMATOUS ACTIVITY AND REDUCE INCREASED CAPILLARY PERMEABILITY.
摘要:
CARRIER-BOUND PROTEINS ARE PREPARED BY REACTING A PROTEIN IN AQUEOUS SOLUTION WITH A COMPOUND HAVING AT LEAST ONE EPOXY GROUP AND AT LEAST ONE ADDITIONAL FUNCTIONAL GROUP CAPABLE OF PRODUCING A BOND WITH A CARRIER MATERIAL, AND REACTING THE RESULTING PRODUCT WITH A CARRIER MATERIAL, OPTIONALLY FORMING THE CARRIER MATERIAL IN SITU BY POLYMERIZATION OF A MONOMER OR MONOMER MIXTURE.
摘要:
Apparatus for the imprinting of dragees wherein the apparatus comprises, in combination, a feed hopper, a rotating cylindrical transport drum having a plurality of receiving apertures adapted to receive dragees from said hopper and to hold dragees, a set of printing rolls disposed on either side of said transport drum to lightly press against both sides of the dragees in the apertures of the transport drum, and inkers for said printing rolls.