Extracurricular laboratory:new discovery of 1-Boc4-hydroxy-3-methylpiperidine

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DUAL NAV1.2/5HT2A INHIBITORS FOR TREATING CNS DISORDERS

Compounds of formula I: I are disclosed, as are pharmaceutical compositions containing such compounds. Methods of treating neurological or psychiatric disorders in a patient in need are also disclosed. Such disorders include depression, bipolar disorder, pain, schizophrenia, obsessive compulsive disorder, addiction, social disorder, attention deficit hyperactivity disorder, an anxiety disorder, autism, a cognitive impairment, or a neuropsychiatric symptom such as apathy, depression, anxiety, psychosis, aggression, agitation, impulse control disorders, and sleep disorders in neurological disorders such as Alzheimer’s and Parkinson’s diseases.

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Reference£º
Piperidine – Wikipedia,
Piperidine | C5H17499N – PubChem

 

Extracurricular laboratory:new discovery of 4-Methoxypiperidine hydrochloride

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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, 4045-25-4, name is 4-Methoxypiperidine hydrochloride, introducing its new discovery. Product Details of 4045-25-4

NOVEL COMPOUNDS

The present invention relates to novel compounds and methods for the manufacture of inhibitors of deubiquitylating enzymes (DUBs). In particular, the invention relates to the inhibition of ubiquitin C-terminal hydrolase L1 (UCHL1). The invention further relates to the use of DUB inhibitors in the treatment of cancer and other indications. Compounds of the invention include compounds having the formula (I) or a pharmaceutically acceptable salt thereof, wherein R1 to R8 are as defined herein.

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Reference£º
Piperidine – Wikipedia,
Piperidine | C5H8370N – PubChem

 

Extracurricular laboratory:new discovery of 1-Cbz-4-(methylsulfonyloxymethyl)piperidine

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Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 159275-16-8, molcular formula is C15H21NO5S, introducing its new discovery. Quality Control of: 1-Cbz-4-(methylsulfonyloxymethyl)piperidine

CYCLOAMINO DERIVATIVES AS GPR119 ANTAGONISTS

Therapeutic compounds are disclosed having the general formula (I) that are useful for the treatment of metabolic disorders, including type II diabetes. The compounds have activity as agonists of GPR119. Compounds having the stereochemistry of formula (la) may also demonstrate DPP-IV inhibitory activity

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Reference£º
Piperidine – Wikipedia,
Piperidine | C5H23637N – PubChem

 

Simple exploration of Methyl 2-piperidinecarboxylate

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HEPATITIS B CORE PROTEIN MODULATORS

The present disclosure provides, in part, compounds having allosteric effector properties against Hepatitis B virus Cp. Also provided herein are methods of treating viral infections, such as hepatitis B, comprising administering to a patient in need thereof a disclosed compound of formula:

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Piperidine – Wikipedia,
Piperidine | C5H7074N – PubChem

 

Brief introduction of 27578-60-5

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Application of 27578-60-5, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.27578-60-5, Name is N-(2-Aminoethyl)piperidine, molecular formula is C7H16N2. In a Article£¬once mentioned of 27578-60-5

Anti-HIV activity of aromatic and heterocyclic thiazolyl thiourea compounds

Several thiazolyl thiourea derivatives were designed and synthesized as non-nucleoside inhibitors (NNRTI) of HIV-1 reverse transcriptase. Six lead compounds were identified that showed subnanomolar IC50 values for the inhibition of HIV replication, were minimally toxic to human peripheral blood mononuclear cells (PBMC) with CC50 values ranging from 28 to >100 muM, and showed remarkably high selectivity indices ranging from 28,000 to >100,000. The most promising compound was N-[1-(1-furoylmethyl)]-N?-[2-(thiazolyl)]thiourea (compound 6), which showed potency against two NNRTI-resistant HIV-1 isolates (A17 and A17 variant) at nanomolar to low micromolar concentrations, exhibited much greater potency against both wild-type as well as NNRTI-resistant HIV-1 than nevirapine, delavirdine, HI-443, and HI-244, was minimally toxic to PBMC, and had a selectivity index of >100,000. The potency and minimal cytotoxicity of these aromatic/heterocyclic thiourea compounds suggest that they may be potentially useful as anti-AIDS drugs.

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Piperidine – Wikipedia,
Piperidine | C5H4380N – PubChem

 

Simple exploration of 4,4′-Bipiperidine dihydrochloride

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Bicyclic fibrinogen antagonists

This invention relates to compounds of the formulae: whereinA1 is O, S, N?R1 or CHR1;A4 is N?R4 or CHR4;R2 is a sidechain containing an acid or ester group;R1, R4 and R5 are substituents such as H, alkyl and aryl alkyl, andR6 is a sidechain containing a nitrogen group; andpharmaceutically acceptable salts thereof,which are effective for inhibiting platelet aggregation, pharmaceutical compositions for effecting such activity, and a method for inhibiting platelet aggregation.

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Piperidine – Wikipedia,
Piperidine | C5H19979N – PubChem

 

Extracurricular laboratory:new discovery of 177-11-7

Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data. Formula: C7H13NO2, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 177-11-7, in my other articles.

Chemistry is an experimental science, Formula: C7H13NO2, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 177-11-7, Name is 1,4-Dioxa-8-azaspiro[4.5]decane

SULFONAMIDES AS INHIBITORS OF BCL-2 FAMILY PROTEINS FOR THE TREATMENT OF CANCER

The present invention includes novel compound and methods of treating a disease or disorder by antagonizing Bcl-2 family proteins, particularly compounds of Formula (I) or pharmaceutically acceptable salt thereof, as well as methods of treating a disease, disorder, or syndrome associated with Bcl-2 inhibition, particularly hyper proliferative diseases. The present invention also includes pharmaceutical compositions including compounds of formula (I) and pharmaceutically acceptable salts thereof

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Reference£º
Piperidine – Wikipedia,
Piperidine | C5H7360N – PubChem

 

The Absolute Best Science Experiment for 392331-66-7

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Electric Literature of 392331-66-7, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.392331-66-7, Name is 1-Boc-4-(Aminomethyl)-4-hydroxypiperidine, molecular formula is C11H22N2O3. In a Patent£¬once mentioned of 392331-66-7

5-AMINO-QUINOLINE-8-CARBOXAMIDE DERIVATIVES AS 5-HT4 RECEPTOR AGONISTS

The present invention relates to novel quinoline compounds of formula (I), and their pharmaceutically acceptable salts and process for their preparation. The compounds of formula (I) are useful in the treatment of various disorders that are related to 5-HT4 receptor agonists.

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Reference£º
Piperidine – Wikipedia,
Piperidine | C5H18622N – PubChem

 

New explortion of 4-Piperidinone

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INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL

The present invention provides compounds of Formula I and the pharmaceutically acceptable salts thereof, which are inhibitors of the ROMK (Kir1.1) channel. The compounds may be used as diuretic and/or natriuretic agents and for the therapy and prophylaxis of medical conditions including cardiovascular diseases such as hypertension, heart failure and chronic kidney disease and conditions associated with excessive salt and water retention.

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Piperidine | C5H130N – PubChem

 

More research is needed about tert-Butyl 4-(4-amino-1H-pyrazol-1-yl)piperidine-1-carboxylate

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PYRIMIDO-DIAZEPINONE COMPOUNDS AND METHODS OF TREATING DISORDERS

The present invention relates to novel pyrimido-diazepinone compounds, methods of modulating protein kinases, including MPS1 (TTK), ERK5 (BMK1, MAPK7), LRKK2, EphA2, polo kinase 1,2,3, or 4, Ackl, Ack2, Abl, DCAMKL1, ABL1, Abl mutants, DCAMKL2, ARK5, BRK, MKNK2, FGFR4, TNK1, PLK1, ULK2, PLK4, PRKD1, PRKD2, PRKD3, ROS1, RPS6KA6, TAOK1, TAOK3, TNK2, Bcr-Abl, GAK, cSrc, TPR-Met, Tie2, MET, FGFR3, Aurora, Axl, Bmx, BTK, c-kit, CHK2, Flt3, MST2, p70S6K, PDGFR, PKB, PKC, Raf, ROCK-H, Rskl, SGK, TrkA, TrkB and TrkC, and the use of such compounds in the treatment of various diseases, disorders or conditions.

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Reference£º
Piperidine – Wikipedia,
Piperidine | C5H21599N – PubChem