Discovery of 4-Amino-1-benzylpiperidine

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Design and development of benzoxazole derivatives with toll-like receptor 9 antagonism

Toll-like receptor 9 (TLR9) is a major therapeutic target for numerous inflammatory disorders. Development of small molecule inhibitors for TLR9 remains largely empirical due to lack of structural understanding of potential TLR9 antagonism by small molecules and due to the unusual topology of the ligand binding surface of the receptor. To develop a structural model for rational design of small molecule TLR9 antagonists, an enhanced homology model of human TLR9 (hTLR9) was constructed. Binding mode analysis of a series of molecules having characteristic molecular geometry, flexibility and basicity was conducted based on crystal structure of the inhibitory DNA (iDNA) bound to horse and bovine TLR9. Interaction with specific amino acid residues in four leucine rich repeat (LRR) regions of TLR9 was identified to be critical for antagonism by small molecules. The biological validation of TLR9 antagonism and its correlation with probe-receptor interactions led to a reliable model that could be used for development of novel small molecules with potent TLR9 antagonism (IC50 30?100?nM) with excellent selectivity against TLR7.

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Piperidine – Wikipedia,
Piperidine | C5H12145N – PubChem

 

More research is needed about 4-Amino-1-benzylpiperidine

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6-Substituted pyrido-pyrimidines

The present invention provides compounds of the Formula I and II: 1wherein R1, R3, W, Z, X1, X2, Ar1, R8 and R9 are as defined herein, and methods and intermediates for their preparation and uses thereof.

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Piperidine – Wikipedia,
Piperidine | C5H12297N – PubChem

 

Top Picks: new discover of 4-Amino-1-benzylpiperidine

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Process for making Boc-protected 3-aminohydantoins/thiohydantoins and 3-aminodihydrouracils/dihydrothiouracils

The present invention provides a process for the efficient assembly of Boc-protected 3-aminohydantoins/thiohydantoins and 3-aminodihydrouracils/dihydrothiouracils via a one-pot solution phase or solid phase synthesis from readily available starting materials.

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Piperidine – Wikipedia,
Piperidine | C5H12304N – PubChem

 

The important role of 4-Amino-1-benzylpiperidine

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Related Products of 50541-93-0, Catalysts are substances that increase the reaction rate of a chemical reaction without being consumed in the process. 50541-93-0, Name is 4-Amino-1-benzylpiperidine, molecular formula is C12H18N2. In a Patent£¬once mentioned of 50541-93-0

6-BENZIMIDAZOLYL-2-MORPHOLINO-4- (AZETIDINE, PYRROLIDINE, PIPERIDINE OR AZEPINE) PYRIMIDINE DERIVATIVES AS PI3K AND MTOR INHIBITORS FOR THE TREATMENT OF PROLIFERATIVE DISORDERS

The invention concerns pyrimidine derivatives of Formula (I): wherein each of p, R1, R2, q, R3, r, R4, s, t, X1 and Q1 have any of the meanings defined in the description; processes for their preparation, pharmaceutical compositions containing them and their use in a method for producing an anti-proliferative effect in a warm blooded animal such as man

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Piperidine – Wikipedia,
Piperidine | C5H12385N – PubChem

 

Extracurricular laboratory:new discovery of 4-Amino-1-benzylpiperidine

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5-(heterocyclic alkyl)-6-aryl-dihydropyrimidines

This invention is directed to dihydropyrimidine compounds of the following formula: STR1which are selective antagonists for human alpha 1A receptors. This invention is also related to uses of these compounds for lowering intraocular pressure, inhibiting cholesterol synthesis, relaxing lower urinary tract tissue, the treatment of benign prostatic hyperplasia, impotency, cardiac arrhythmia and for the treatment of any disease where antagonism of the alpha 1A receptor may be useful. The invention further provides a pharmaceutical composition comprising a therapeutically effective amount of the above-defined compounds and a pharmaceutically acceptable carrier.

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Piperidine – Wikipedia,
Piperidine | C5H12177N – PubChem

 

Final Thoughts on Chemistry for 50541-93-0

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TRIAZOLONE, TETRAZOLONE AND IMIDAZOLONE DERIVATIVES FOR USE AS ALPHA-2C ADRENORECEPTOR ANTAGONISTS

The present invention concerns substituted triazolone, tetrazolone and imidazolone derivatives according to the general Formula (I) a pharmaceutically acceptable acid or base addition salt thereof, a stereochemically isomeric form thereof, an N-oxide form thereof or a quaternary ammonium salt thereof, wherein the variables are defined in Claim 1, having selective E2C-adrenoceptor antagonist activity. It further relates to their preparation, compositions comprising them and their use as a medicine. The compounds according to the invention are usefull for the prevention and/or treatment of central nervous system disorders, mood disorders, anxi-ety disorders, stress-related disorders associated with depression and/or anxiety, cognitive disorders, personality disorders, schizoaffective disorders, Parkinson’s disease, dementia of the Alzheimer’s type, chronic pain conditions, neurodegenerative diseases, addiction disorders, mood disorders and sexual dysfunction.

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Piperidine – Wikipedia,
Piperidine | C5H12319N – PubChem

 

More research is needed about 4-Amino-1-benzylpiperidine

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 50541-93-0, help many people in the next few years.Computed Properties of C12H18N2

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, Computed Properties of C12H18N2, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 50541-93-0, Name is 4-Amino-1-benzylpiperidine, molecular formula is C12H18N2. In a Patent, authors is £¬once mentioned of 50541-93-0

Methods and compounds for inhibiting beta-amyloid peptide release and/or its synthesis

Disclosed are compounds which inhibit beta-amyloid peptide release and/or its synthesis, and, accordingly, have utility in treating Alzheimer’s disease. Also disclosed pharmaceutical compositions comprising a compound which inhibits beta-amyloid peptide release and/or its synthesis as well as methods for treating Alzheimer’s disease both prophylactically and therapeutically with such pharmaceutical compositions.

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Piperidine – Wikipedia,
Piperidine | C5H11862N – PubChem

 

Simple exploration of 50541-93-0

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 50541-93-0 is helpful to your research. Application In Synthesis of 4-Amino-1-benzylpiperidine

In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 50541-93-0, name is 4-Amino-1-benzylpiperidine, introducing its new discovery. Application In Synthesis of 4-Amino-1-benzylpiperidine

Hit-to-lead optimization of novel 2-alkylaminomethylquinoline derivatives as anti-chagas agents

Chagas disease is one of the main neglected diseases in the world, being endemic in 21 countries of Latin America. This disease has become a global health problem due to migration of infected people non-endemic countries. Even though this disease affects millions of people, only two drugs are approved for its treatment, benznidazole and nifurtimox, and both have several limitations. We have previously reported the synthesis and biological activity against T. cruzi of polysubstituted quinolines analogous to natural products. Herein, we present the synthesis of rationally-based novel analogous of this family of compounds. All the evaluated compounds presented trypanocidal activity. Three of them (6, 7 and 10) stand out for their selectivity indexes. Ethyl 2-((4-benzyl-1,4-diazepan-1-yl)methyl)-6-chloro-4-phenylquinoline-3-carboxylate (compound 10) was found to display anti-parasite activity, presenting the highest selectivity index. Apart from controlling in vivo the parasitemia levels, compound 10 was able to prevent tissue inflammation, a key factor to prevent the progression to chronic chagasic cardiomyopathy. The therapeutic effects of compound 10 are promising and suggest a new possibility to treat this disease.

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Piperidine – Wikipedia,
Piperidine | C5H11906N – PubChem

 

Simple exploration of 4-Amino-1-benzylpiperidine

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ISOINDOLINE COMPOUNDS FOR USE IN THE TREATMENT OF CANCER

Provided herein are isoindoline compounds such as those of formula (I), pharmaceutical compositions comprising one or more of such compounds, and methods of their use for treating, preventing, or managing various diseases. Formula (I)

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Reference£º
Piperidine – Wikipedia,
Piperidine | C5H12444N – PubChem

 

More research is needed about 4-Amino-1-benzylpiperidine

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 50541-93-0 is helpful to your research. Product Details of 50541-93-0

In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 50541-93-0, name is 4-Amino-1-benzylpiperidine, introducing its new discovery. Product Details of 50541-93-0

CHEMICAL COMPOUNDS

The use of a compound of formula (I) or a pharmaceutically acceptable salt or solvate thereof, wherein X1, X2, X3, X4, Ra, p, R1,Z,Y, R2, R3 and R4 are as defined in the specification, in the preparation of a medicament for the treatment of C-C chemokine mediated conditions, such as inflammatory disease. Certain compounds of formula (I) are novel and these, together with their preparation are also described and claimed.

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Reference£º
Piperidine – Wikipedia,
Piperidine | C5H12189N – PubChem