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OXAZOLIDINONE COMPOUNDS AND THEIR USES IN PHARMACEUTICALS

The invention relates to the field of blood coagulation, more specifically it relates to novel oxazolidinone compounds or a pharmaceutically acceptable salt thereof, and their uses in the manufacture of medicaments for treating thromboembolic disorders or inhibiting factor Xa.

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Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H263NO – PubChem

 

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FUSED BICYCLIC PYRAZOLE DERIVATIVES AS KINASE INHIBITORS

A series of substituted pyrazolo[1,5-alpha][1,3,5]triazine and pyrazolo[1,5-alpha]-pyrimidine derivatives, being selective inhibitors of PI3 kinase enzymes, are accordingly of benefit in medicine, for example in the treatment of inflammatory, autoimmune, cardiovascular, neurodegenerative, metabolic, ontological, nociceptive or ophthalmic conditions. Formula (I)

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Oxazolidine – Wikipedia,
Oxazolidine | C3H10NO – PubChem

 

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RADIOLABELED COMPOUNDS AND THEIR USE AS RADIOTRACERS FOR QUANTITATIVE IMAGING OF PHOSPHODIESTERASE (PDE10A) IN MAMMALS

The present invention provides radiolabeled compounds useful as radiotracers for quantitative imaging of PDE10A in mammals. The compound of the present invention is represented by the formula (I): wherein each symbols are as defined in the specification.

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Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H232NO – PubChem

 

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In heterogeneous catalysis, the catalyst is in a different phase from the reactants. SDS of cas: 497-25-6, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 497-25-6, name is Oxazolidin-2-one. In an article£¬Which mentioned a new discovery about 497-25-6

INHIBITORS OF POLO-LIKE KINASE

The present invention provides compounds having a structure according to Formula (I): or a salt or solvate thereof, wherein ring A, U1, U2, U3, R2, R3 and R4 are defined herein. The invention further provides pharmaceutical compositions including the compounds of the invention and methods of making and using the compounds and compositions of the invention, e.g., in the treatment and prevention of various disorders, such as Parkinson?s disease.

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Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H182NO – PubChem

 

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Preparation pepper hydrochloride and berberine method (by machine translation)

The present invention provides a process for preparing pepper hydrochloride and berberine method. The preparation pepper ethylamine hydrochloride method comprises the following steps: adding organic solvent in the heliotropin, condition and under stirring, dropping 2 – oxazolidine […]; after the reaction is complete, the reaction system is poured into the hydrochloric acid aqueous solution in the hydrochlorination; adjusting the pH value, filtered to obtain product pepper hydrochloride. Preparation berberine method, said method comprising: using the method to prepare the pepper hydrochloride. The present invention provides a method and application, few steps and is simple in operation, without the use of expensive raw materials and toxic substances, environmental protection, and the cost is low. (by machine translation)

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Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H116NO – PubChem

 

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5-BENZYLAMINOMETHYL-6-AMINOPYRAZOLO[3,4-B]PYRIDINE DERIVATIVES AS CHOLESTERYL ESTER-TRANSFER PROTEIN (CETP) INHIBITORS USEFUL FOR THE TREATMENT OF ATHEROSCLEROSIS

The present application relates to a series of substituted pyrazolopyridin-6-amines having the general formula (I), including their stereoisomers and/or their pharmaceutically acceptable salts. Where in R, R1, R2, Ra, Raa, Rb and n are as defined here in. The present invention further relates to pharmaceutical compositions comprising compounds of formula (I). The compounds of this application are useful as CETP inhibitors for increasing HDL cholesterol and decreasing LDL cholesterol in a patient.

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Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H37NO – PubChem

 

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The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 497-25-6 is helpful to your research. Electric Literature of 497-25-6

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Extensive dataset for oxidative degradation of ethanolamine at 55-75 C and oxygen concentrations from 6 to 98%

Post combustion CO2 capture using amines as chemical absorbents is a relatively mature technology. Rate of reaction and desorption energy demand are normally prime criteria for evaluation of new solvents while degradation and corrosion studies are often postponed. However, degradation and corrosion are in many cases showstoppers and should be considered at an early stage. In this work, a systematic study has been conducted on oxidative degradation of 30 wt% ethanolamine (MEA) for oxygen concentrations: 6, 21, 49 and 98% and temperatures: 55, 65 and 75 C. The formation of ten primary degradation compounds (acids, ammonia and alkyl amines) and seven secondary degradation compounds (HEGly, OZD, HEPO, HEF, HEA, HEI and BHEOX was monitored as function of time over a period of 3-6 weeks. The full comprehensive data set is available in the supplementary information for development of models describing the degradation behavior. Suggested mechanisms for formation of seven secondary degradation compounds; HEGly, HEPO, OZD, HEF, HEA, BHEOX and HEI from literature were compiled and discussed in view of the experimental results to suggest pathways which are more likely than others.The rate of MEA degradation increases with increasing temperature and oxygen concentration. The overall nitrogen balances were closed within 83-97%; the higher deviations observed at the highest temperature, 75 C. HEF, HEI and ammonia were the degradation compounds that most significantly contributed to the nitrogen balance in most experiments. However, at 6% O2 content, HEGly was the major nitrogen containing degradation compound identified. Formate was found to be the major anionic compound in all experiments.HEGly formation was found to be independent on O2 partial pressure, but this may not be true for the further reaction of HEGly. The results suggests OZD formation to be oxygen dependent. However, only one mechanism is so far suggested for an oxygen dependent pathway. Both OZD and HEPO concentrations increase with oxygen concentration. Separate laboratory experiments at constant temperature (55-75 C) do not capture the HEPO formation seen in pilot plant samples indicating that higher temperatures and/or temperature cycles are necessary.The results clearly show that performing accelerated degradation tests with 98% oxygen cannot easily be extrapolated to what happens at 6% oxygen, and therefore may not be representative for the situation in an industrial plant both with regard to rates of formation and products formed.

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Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H1098NO – PubChem

 

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Microwave-assisted preparation of cyclic ureas from diamines in the presence of ZnO

A MW-assisted direct synthesis of cyclic ureas has been developed that proceeds expeditiously in the presence of ZnO thus shortening its reaction time; the process also eliminates the formation of byproducts when compared to the traditional methods involving conventional heating. A microwave-assisted facile method for the preparation of various ureas, cyclic ureas, and urethanes has been developed that affords nearly quantitative yield of products at 120C (150 W), 71 kPa within 10 min using ZnO as a catalyst. The enhanced selectivity in this reaction is attributed to the deployment of ZnO whose absence results in poor yield and the generation of byproducts.

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Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H692NO – PubChem

 

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We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 497-25-6, and how the biochemistry of the body works.Application of 497-25-6

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Oxidative degradation of amines using a closed batch system

Oxidative degradation experiments on five amines and two amino acids were performed in a new closed setup at atmospheric pressure. For most of the amines/amino acids significant degradation was not present under these conditions, except for MEA and MMEA. The degradation compounds found seem to follow the same patterns as described in literature. Volatile compounds as ammonia and alkylamine play an important role in understanding the initial degradation mechanisms. For MMEA, methylamine and ammonia were found in the same order of magnitude. Oxygen stochiometry of the degradation compounds could not be explained by initial air in the system. Oxygen in some of the degradation compounds could come from oxygen diffusing into the system as seen from proposed model and/or water reacting with iminium giving aldehyde and amine/ammonia. Temperature and dissolved metal seemed to influence oxygen and degradation rate for the MEA experiments.

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Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H1091NO – PubChem

 

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We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 497-25-6, and how the biochemistry of the body works.Synthetic Route of 497-25-6

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Synthesis of a Triphenylphosphine Reagent on Non-cross-linked Polystyrene Support: Application to the Staudinger/Aza-Wittig Reaction

formula presented A new triphenylphosphine reagent linked to a linear polystyrene was synthesized. The reactivity of this phosphine-bound polymer is superior to that of the phosphine bound to cross-linked polystyrene. The polymer reacted very rapidly with azides to generate iminophosphoranes which could then react with aldehydes to generate imines in good yields and high purities.

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Reference£º
Oxazolidine – Wikipedia,
Oxazolidine | C3H415NO – PubChem