4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide - 199433-58-4

4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide

Catalog Number: EVT-254330
CAS Number: 199433-58-4
Molecular Formula: C16H16N4O
Molecular Weight: 280.32 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
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Product Introduction

Description
4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide is a chemical compound that has gained significant attention in the scientific community due to its potential therapeutic and environmental applications. This paper aims to provide a comprehensive overview of the synthesis, chemical structure, biological activity, and potential applications of this compound.
Applications in Various Fields
The potential applications of 4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide in medical, environmental, and industrial research are vast.
In medical research, this compound has shown potential as a therapeutic agent for various diseases, including cancer, autoimmune disorders, and inflammatory diseases. Clinical trials are ongoing to evaluate its safety and efficacy in humans.
In environmental research, 4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide can be used to study its effects on ecosystems and its role in pollution management. This compound has shown potential as a sustainable and environmentally friendly alternative to traditional chemical pollutants.
In industrial research, this compound can be used in manufacturing processes to improve product quality and efficiency. Health and safety considerations are crucial in the industrial use of this compound, and best practices should be adopted to minimize its impact on human health and the environment.

Properties

CAS Number

199433-58-4

Product Name

4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide

IUPAC Name

4-[(1R)-1-aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide

Molecular Formula

C16H16N4O

Molecular Weight

280.32 g/mol

InChI

InChI=1S/C16H16N4O/c1-10(17)11-2-4-12(5-3-11)16(21)20-14-7-9-19-15-13(14)6-8-18-15/h2-10H,17H2,1H3,(H2,18,19,20,21)/t10-/m1/s1

InChI Key

JTVBXQAYBIJXRP-SNVBAGLBSA-N

SMILES

CC(C1=CC=C(C=C1)C(=O)NC2=C3C=CNC3=NC=C2)N

Synonyms

4-(1-aminoethyl)-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide

Canonical SMILES

CC(C1=CC=C(C=C1)C(=O)NC2=C3C=CNC3=NC=C2)N

Isomeric SMILES

C[C@H](C1=CC=C(C=C1)C(=O)NC2=C3C=CNC3=NC=C2)N
Method of Synthesis or Extraction
The synthesis of 4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide can be achieved through various methods, including chemical synthesis and extraction from natural sources. Chemical synthesis involves the reaction of 4-aminobenzamide with 1H-pyrrolo[2,3-b]pyridine-4-carboxylic acid, followed by the addition of (1R)-1-aminoethylamine. The yield and efficiency of this method depend on the reaction conditions, such as temperature, pressure, and reaction time.
Extraction from natural sources involves the isolation of the compound from plants or microorganisms that produce it. This method is often preferred due to its sustainability and environmental benefits. However, the yield and efficiency of this method can be affected by factors such as the availability of the source material and the extraction process used.
Environmental and safety considerations are crucial in the synthesis and extraction of 4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide. Chemical synthesis can produce hazardous waste and byproducts that can harm the environment and human health. Extraction from natural sources can also have environmental impacts if not done sustainably. Therefore, it is essential to consider the environmental and safety implications of each method and adopt best practices to minimize their impact.
Chemical Structure and Biological Activity
The chemical structure of 4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide consists of a benzamide group, a pyrrolopyridine ring, and an aminoethyl group. This compound has shown promising biological activity, particularly in its ability to target specific biological pathways.
The mechanism of action of 4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide involves the inhibition of specific enzymes or receptors involved in cell signaling pathways. This compound has been shown to target various biological pathways, including the PI3K/Akt/mTOR pathway, which is involved in cell growth and survival, and the JAK/STAT pathway, which is involved in immune response and inflammation.
The bioactivity and potency of 4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide have been demonstrated in various preclinical studies. This compound has shown potential as a therapeutic agent for various diseases, including cancer, autoimmune disorders, and inflammatory diseases.
Biological Effects
The biological effects of 4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide on cell function and signal transduction have been extensively studied. This compound has been shown to inhibit cell proliferation, induce apoptosis, and modulate immune response and inflammation.
The potential therapeutic and toxic effects of 4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide have also been investigated. This compound has shown promising therapeutic effects in preclinical studies, but its toxicity and safety profile need further evaluation.
Future Perspectives and Challenges
The current limitations in the use and study of 4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide include its toxicity and safety profile, as well as the need for further evaluation of its efficacy in humans. Possible solutions and improvements include the development of more efficient and sustainable synthesis methods and the identification of new biological targets for this compound.
Future trends and prospects in the application of 4-[(1R)-1-Aminoethyl]-N-(1H-pyrrolo[2,3-b]pyridin-4-yl)benzamide in scientific research include the development of new therapeutic applications and the exploration of its potential in environmental and industrial research. The continued study of this compound is essential to fully understand its potential benefits and limitations.

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