Category: 81363-14-6

Related Products of 81363-14-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.81363-14-6, Name is 1-(2,2,2-Trifluoroethyl)piperidin-4-one, molecular formula is C7H10F3NO. In a Patent，once mentioned of 81363-14-6

The present invention relates to substituted tetrahydropyridothienopyrimidine compounds of general formula(I)as described and defined herein, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyperproliferative and/or angiogenesis disorder, as a sole agent or in combination with other active ingredients.

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 81363-14-6

Reference：
Piperidine – Wikipedia,
Piperidine | C5H10932N – PubChem

 

A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, category: piperidines, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 81363-14-6, Name is 1-(2,2,2-Trifluoroethyl)piperidin-4-one, molecular formula is C7H10F3NO. In a Patent, authors is ，once mentioned of 81363-14-6

The present invention provides a compound having a lysine specific demethylase 1 inhibitory action, and useful as a medicament such as a prophylactic or therapeutic agent for schizophrenia, Alzheimer’s disease, Parkinson’s disease or Huntington’s disease, and the like. The present invention relates to a compound represented by the formula wherein A is a hydrocarbon group optionally having substituent(s), or a heterocyclic group optionally having substituent(s); B is a benzene ring optionally having further substituent(s); R1, R2 and R3 are each independently a hydrogen atom, a hydrocarbon group optionally having substituent(s), or a heterocyclic group optionally having substituent(s); A and R1 are optionally bonded to each other to form, together with the adjacent nitrogen atom, a cyclic group optionally having substituent(s); and R2 and R3 are optionally bonded to each other to form, together with the adjacent nitrogen atom, a cyclic group optionally having substituent(s), or a salt thereof.

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 81363-14-6, help many people in the next few years.category: piperidines

Reference：
Piperidine – Wikipedia,
Piperidine | C5H10936N – PubChem

 

Chemistry is traditionally divided into organic and inorganic chemistry. category: piperidines. The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent£¬Which mentioned a new discovery about 81363-14-6

NICOTINAMIDE DERIVATIVES

The present invention relates to compounds formula (I) and pharmaceutically acceptable salts and solvates thereof, wherein the substituents are as defined herein, compositions containing such compounds and the uses of such compounds for the treatment of various diseases and conditions such as asthma

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.category: piperidines, you can also check out more blogs about81363-14-6

Reference£º
Piperidine – Wikipedia,
Piperidine | C5H10933N – PubChem