Buy 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride (BT-254449)

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1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride

Catalog Number: BT-254449

CAS Number: 1257326-24-1

Molecular Formula: C15H22ClN3O

Molecular Weight: 295.811

The product is for non-human research only. Not for therapeutic or veterinary use.

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Product Introduction

Description

1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride, also known as PIMIH, is a synthetic compound that belongs to the class of imidazolidinones. It has gained significant attention in the scientific community due to its potential therapeutic and industrial applications.

Properties

CAS Number

1257326-24-1

Product Name

1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride

IUPAC Name

1-phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one;hydrochloride

Molecular Formula

C15H22ClN3O

Molecular Weight

295.811

InChI

InChI=1S/C15H21N3O.ClH/c19-15-17(12-13-6-4-5-9-16-13)10-11-18(15)14-7-2-1-3-8-14;/h1-3,7-8,13,16H,4-6,9-12H2;1H

InChI Key

BYJUVPWUMBVSTK-UHFFFAOYSA-N

SMILES

C1CCNC(C1)CN2CCN(C2=O)C3=CC=CC=C3.Cl

Synonyms

4,5-Dihydro-1-phenyl-3-(2-piperidinyl)methylimidazol-2(1H)-one

Method of Synthesis or Extraction

1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride can be synthesized using various methods, including the reaction of 1-phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one with hydrochloric acid. The efficiency and yield of each method depend on the reaction conditions, such as temperature, pressure, and catalysts. However, the synthesis of 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride requires careful consideration of environmental and safety considerations, as some of the reactants and by-products can be hazardous.

Chemical Structure and Biological Activity

1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride has a unique chemical structure that consists of an imidazolidinone ring, a phenyl group, and a piperidine group. The compound has shown promising biological activity, particularly in the field of medicinal chemistry. 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride has been found to act as an inhibitor of various enzymes and receptors, including acetylcholinesterase, monoamine oxidase, and adenosine receptors. These biological targets make 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride a potential candidate for the treatment of various diseases, such as Alzheimer's disease, Parkinson's disease, and cancer.

Biological Effects

1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride has been shown to have significant effects on cell function and signal transduction. The compound has been found to modulate the activity of various signaling pathways, including the MAPK/ERK and PI3K/Akt pathways. 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride has also been shown to induce apoptosis in cancer cells, making it a potential anticancer agent. However, the compound's potential therapeutic effects must be balanced against its potential toxic effects, which can vary depending on the dose and duration of exposure.

Applications

1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride has various applications in medical, environmental, and industrial research. In medical research, 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride's role in drug development has been extensively studied, with promising results in preclinical studies. Clinical trials are currently underway to evaluate the compound's safety and efficacy in humans. In environmental research, 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride's effects on ecosystems and its role in pollution management have been studied. In industrial research, 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride has been used in manufacturing processes to improve product quality and efficiency. However, the compound's health and safety considerations must be carefully evaluated before its use in industrial applications.

Future Perspectives and Challenges

Despite the promising results obtained from preclinical studies, the use of 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride in clinical settings faces several challenges. The compound's pharmacokinetics and pharmacodynamics must be thoroughly evaluated to determine the optimal dose and duration of treatment. Additionally, the compound's potential toxic effects must be carefully monitored to ensure patient safety. Future research should focus on developing more efficient and safer methods of synthesis and extraction, as well as identifying new biological targets for 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride.
Conclusion:
In conclusion, 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride is a synthetic compound with significant potential in various fields of research. Its unique chemical structure and biological activity make it a promising candidate for the treatment of various diseases. However, the compound's potential therapeutic effects must be balanced against its potential toxic effects, and its use in clinical and industrial settings must be carefully evaluated. Future research should focus on developing more efficient and safer methods of synthesis and extraction, as well as identifying new biological targets for 1-Phenyl-3-(piperidin-2-ylmethyl)imidazolidin-2-one hydrochloride.

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