Tag: M.W:100-200

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent£¬ name: 1-Methylpiperidin-4-ol, Which mentioned a new discovery about 106-52-5

A Benz wicked zuozuo apperception compound derivative and its application (by machine translation)

The present invention provides a Benz wicked zuozuo apperception compound derivative and its application, in vitro receptor binding test shows, the present invention provides the compounds of H3 Receptor has high affinity, can be used for improving the central nervous system disease, such as schizophrenia, cognitive disorders, pain, sleeping and the like; with the H1 Low receptor affinity, and then will not produce a side effect. (by machine translation)

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, name: 1-Methylpiperidin-4-ol, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 106-52-5

Reference£º
Piperidine – Wikipedia,
Piperidine | C5H2359N – PubChem

 

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, name: 4,4-Difluoropiperidine, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 21987-29-1, Name is 4,4-Difluoropiperidine, molecular formula is C5H9F2N. In a Patent, authors is £¬once mentioned of 21987-29-1

PIPERIDINYLPYRAZOLOPYRIMIDINONES AND THEIR USE

The present application relates to novel substituted piperidinylpyrazolopyrimidinones, to processes for their preparation, the compounds for use alone or in combinations in a method for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of acute and recurrent bleeding in patients with or without underlying hereditary or acquired hemostatic disorders, wherein the bleeding is associated with a disease or medical intervention selected from the group consisting of heavy menstrual bleeding, postpartum hemorrhage, hemorrhagic shock, hemorrhagic cystitis, gastrointestinal hemorrhage, trauma, surgery, transplantation, stroke, liver diseases, hereditary angioedema, nosebleed, and synovitis and cartilage damage following hemarthrosis.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 21987-29-1, help many people in the next few years.name: 4,4-Difluoropiperidine

Reference£º
Piperidine – Wikipedia,
Piperidine | C5H3007N – PubChem

 

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent£¬ Safety of Piperidin-4-one hydrochloride, Which mentioned a new discovery about 41979-39-9

TRICYCLIC COMPOUNDS FOR THE TREATMENT OF INFLAMMATORY DISORDERS

The present invention provides compounds represented by general formula (1) wherein, R1 R2, R3, R4, R5, R6, R7, R8, R9, R10, R11, R12, R13 and X are as defined in the specification, in all its stereoisomeric and tautomeric forms and mixtures thereof in all ratios, and its pharmaceutically acceptable salts, pharmaceutically acceptable solvates, pharmaceutically acceptable polymorphs and prodrugs. These compounds are useful for treatment of inflammatory disorders including those caused by elevated levels of proinflammatory cytokines such as Tumor Necrosis Factor (TNF-alpha and/or interleukins (IL-1beta, IL-6, IL-8). The invention also relates to processes for the manufacture of compounds of formula (1) and pharmaceutical compositions containing them.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 41979-39-9, help many people in the next few years.Safety of Piperidin-4-one hydrochloride

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Piperidine – Wikipedia,
Piperidine | C5H5856N – PubChem

 

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Application In Synthesis of 3-(Piperidin-1-yl)propanoic acid, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 26371-07-3, Name is 3-(Piperidin-1-yl)propanoic acid, molecular formula is C8H15NO2. In a Patent, authors is £¬once mentioned of 26371-07-3

ANTAGONISTS OF MELANIN CONCENTRATING HARMONE EFFECTS ON THE MELANIN CONCENTRATING HARMONE RECEPTOR

The present invention is directed to compounds of formula (I), which antagonize of the effects of melanin-concentrating hormone (MCH) through the melanin concentrating hormone receptor which is useful for the prevention or treatment of eating disorders, weight gain, obesity, abnormalities in reproduction and sexual behavior, thyroid hormone secretion, diuresis and water/electrolyte homeostasis, sensory processing, memory, sleeping, arousal, anxiety, depression, seizures, neurodegeneration and psychiatric disorders.

I hope this article can help some friends in scientific research. I am very proud of our efforts over the past few months and hope to 26371-07-3, help many people in the next few years.Application In Synthesis of 3-(Piperidin-1-yl)propanoic acid

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Piperidine – Wikipedia,
Piperidine | C5H9126N – PubChem

 

Related Products of 2971-79-1, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.2971-79-1, Name is Methyl piperidine-4-carboxylate, molecular formula is C7H13NO2. In a Article£¬once mentioned of 2971-79-1

Synthesis of 5-amino-2-aminoalkyl-1,3-oxazol-4-ylphosphonic acid derivatives and their use in the preparation of phosphorylated peptidomimetics

Starting from phthalimidoalkanoylamines 1 (amino-protected derivatives of glycine, beta-alanine, gamma-amino butyric, delta-amino valeric, and epsilon-amino caproic acids), a facile synthetic method has been developed to obtain diethyl 5-alkyl(dialkyl)amino-2-aminoalkyl-1,3-oxazol-4-ylphosphonates 7, which have been further used in the preparation of phosphorylated peptidomimetics 10 and 12.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 2971-79-1 is helpful to your research. Related Products of 2971-79-1

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Piperidine – Wikipedia,
Piperidine | C5H8027N – PubChem

 

Application of 762240-09-5, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.762240-09-5, Name is 4-(1H-Pyrazol-1-yl)piperidine, molecular formula is C8H13N3. In a Patent£¬once mentioned of 762240-09-5

MUSCARINIC AGONISTS

This invention relates to compounds that are agonists of the muscarinic M4 receptor and/or M4 receptor and which are useful in the treatment of muscarinic M1/M4 receptor mediated diseases. Also provided are pharmaceutical compositions containing the compounds and the therapeutic uses of the compounds. Compounds include those according to formula 1a or a salt thereof, wherein n, p, Q, R1, R2, R3, R9 and R4 are as defined herein.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 762240-09-5

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Piperidine – Wikipedia,
Piperidine | C5H8332N – PubChem

 

Chemistry is an experimental science, HPLC of Formula: C9H20N2, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 36768-62-4, Name is 4-Amino-2,2,6,6-tetramethylpiperidine

Synthesis and characterization of a persistent paramagnetic rotaxane based on alpha-cyclodextrin

The synthesis and spectroscopic properties of a novel paramagnetic [2]rotaxane is described. This rotaxane is made from molecules having an alkyl chain flanked by 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) groups. Complexation of sebacoyl chloride by alpha-cyclodextrin followed by reaction with a bulky aminonitroxide resulted in the trapping of the cyclodextrin, threaded by the alkyl chain, thus generating the rotaxane structure. The structure of the paramagnetic [2]rotaxane was fully characterized by ESIMS, 1D and 2D NMR and ESR spectroscopy.

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. HPLC of Formula: C9H20N2, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 36768-62-4, in my other articles.

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Piperidine – Wikipedia,
Piperidine | C5H8607N – PubChem

 

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent£¬ Application In Synthesis of N,N-Dimethylpiperidin-4-amine, Which mentioned a new discovery about 50533-97-6

Discovery of a 5 H-benzo[4,5]cyclohepta[1,2-b ]pyridin-5-one (MK-2461) inhibitor of c-Met kinase for the treatment of cancer

c-Met is a transmembrane tyrosine kinase that mediates activation of several signaling pathways implicated in aggressive cancer phenotypes. In recent years, research into this area has highlighted c-Met as an attractive cancer drug target, triggering a number of approaches to disrupt aberrant c-Met signaling. Screening efforts identified a unique class of 5H-benzo[4,5] cyclohepta[1,2-b]pyridin-5-one kinase inhibitors, exemplified by 1. Subsequent SAR studies led to the development of 81 (MK-2461), a potent inhibitor of c-Met that was efficacious in preclinical animal models of tumor suppression. In addition, biochemical studies and X-ray analysis have revealed that this unique class of kinase inhibitors binds preferentially to the activated (phosphorylated) form of the kinase. This report details the development of 81 and provides a description of its unique biochemical properties.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Application In Synthesis of N,N-Dimethylpiperidin-4-amine, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 50533-97-6

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Piperidine – Wikipedia,
Piperidine | C5H3950N – PubChem

 

Application of 41979-39-9, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.41979-39-9, Name is Piperidin-4-one hydrochloride, molecular formula is C5H10ClNO. In a Article£¬once mentioned of 41979-39-9

Multidimensional SuFEx Click Chemistry: Sequential Sulfur(VI) Fluoride Exchange Connections of Diverse Modules Launched From An SOF4 Hub

Sulfur(VI) fluoride exchange (SuFEx) is a new family of click chemistry based transformations that enable the synthesis of covalently linked modules via SVI hubs. Here we report thionyl tetrafluoride (SOF4) as the first multidimensional SuFEx connector. SOF4 sits between the commercially mass-produced gases SF6 and SO2F2, and like them, is readily synthesized on scale. Under SuFEx catalysis conditions, SOF4 reliably seeks out primary amino groups [R-NH2] and becomes permanently anchored via a tetrahedral iminosulfur(VI) link: R?N=(O=)S(F)2. The pendant, prochiral difluoride groups R?N=(O=)SF2, in turn, offer two further SuFExable handles, which can be sequentially exchanged to create 3-dimensional covalent departure vectors from the tetrahedral sulfur(VI) hub.

The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 41979-39-9 is helpful to your research. Application of 41979-39-9

Reference£º
Piperidine – Wikipedia,
Piperidine | C5H5987N – PubChem

 

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Recommanded Product: 177-11-7, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 177-11-7, Name is 1,4-Dioxa-8-azaspiro[4.5]decane, molecular formula is C7H13NO2. In a Patent, authors is £¬once mentioned of 177-11-7

AMINOPIPERIDINE DERIVATIVES, PREPARATION THEREOF AND THERAPEUTIC USE THEREOF

The present invention relates to compounds of formula (I) as defined herein that are melanocortin receptor agonists, to the preparation thereof and to the therapeutic use thereof in the treatment and in the prevention of obesity, diabetes and sexual dysfunctions that can affect both sexes, in the treatment of cardiovascular diseases, and also in anti-inflammatory uses or in the treatment of alcohol dependency.

Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. I hope my blog about is helpful to your research. Recommanded Product: 177-11-7

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Piperidine – Wikipedia,
Piperidine | C5H7299N – PubChem