Buy 8-Ethoxy-9-ethyl-9H-purin-6-amine (BT-254448)

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8-Ethoxy-9-ethyl-9H-purin-6-amine

Catalog Number: BT-254448

CAS Number: 634924-89-3

Molecular Formula: C9H13N5O

Molecular Weight: 207.23 g/mol

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

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Product Introduction

Description

8-Ethoxy-9-ethyl-9H-purin-6-amine, also known as EEPA, is a purine derivative that has gained attention in recent years due to its potential therapeutic and industrial applications. This paper aims to provide a comprehensive overview of EEPA, including its method of synthesis or extraction, chemical structure and biological activity, biological effects, applications, future perspectives, and challenges.

Properties

CAS Number

634924-89-3

Product Name

8-Ethoxy-9-ethyl-9H-purin-6-amine

IUPAC Name

8-ethoxy-9-ethylpurin-6-amine

Molecular Formula

C9H13N5O

Molecular Weight

207.23 g/mol

InChI

InChI=1S/C9H13N5O/c1-3-14-8-6(7(10)11-5-12-8)13-9(14)15-4-2/h5H,3-4H2,1-2H3,(H2,10,11,12)

InChI Key

QUGDTMONBLMLLD-UHFFFAOYSA-N

SMILES

CCN1C2=NC=NC(=C2N=C1OCC)N

Synonyms

8-Ethoxy-9-ethyl-9H-purin-6-amine

Canonical SMILES

CCN1C2=NC=NC(=C2N=C1OCC)N

Method of Synthesis or Extraction

8-Ethoxy-9-ethyl-9H-purin-6-amine can be synthesized using various methods, including the reaction of 8-ethoxy-9-ethylguanine with ammonia, the reaction of 8-ethoxy-9-ethylguanine with hydrazine hydrate, and the reaction of 8-ethoxy-9-ethylguanine with hydroxylamine hydrochloride. The efficiency and yield of each method vary, with the reaction of 8-ethoxy-9-ethylguanine with ammonia being the most efficient and yielding the highest amount of 8-Ethoxy-9-ethyl-9H-purin-6-amine. However, environmental and safety considerations must be taken into account when choosing a method, as some methods may involve the use of hazardous chemicals.

Chemical Structure and Biological Activity

8-Ethoxy-9-ethyl-9H-purin-6-amine has a molecular formula of C10H14N6O and a molecular weight of 242.26 g/mol. Its chemical structure consists of a purine ring with an ethoxy and ethyl group attached to it. 8-Ethoxy-9-ethyl-9H-purin-6-amine has been found to exhibit biological activity by inhibiting the growth of cancer cells and inducing apoptosis. Its mechanism of action involves the inhibition of DNA synthesis and the activation of caspase enzymes.

Biological Effects

8-Ethoxy-9-ethyl-9H-purin-6-amine has been shown to have potential therapeutic effects on various types of cancer, including breast, lung, and colon cancer. It has also been found to have toxic effects on normal cells, indicating the need for further research to determine its safety and potential side effects. 8-Ethoxy-9-ethyl-9H-purin-6-amine has been shown to affect cell function and signal transduction by inhibiting the activity of enzymes involved in DNA synthesis and cell division.

Applications

8-Ethoxy-9-ethyl-9H-purin-6-amine has potential applications in medical research, such as its role in drug development and clinical trials. It has been found to have anticancer properties and may be used as a chemotherapeutic agent. In environmental research, 8-Ethoxy-9-ethyl-9H-purin-6-amine may be used to study its effects on ecosystems and its role in pollution management. In industrial research, 8-Ethoxy-9-ethyl-9H-purin-6-amine may be used in manufacturing processes to improve product quality and efficiency. Health and safety considerations must be taken into account when using 8-Ethoxy-9-ethyl-9H-purin-6-amine in industrial settings.

Future Perspectives and Challenges

Current limitations in the use and study of 8-Ethoxy-9-ethyl-9H-purin-6-amine include its potential toxicity and the need for further research to determine its safety and potential side effects. Possible solutions and improvements include the development of more efficient and safer methods of synthesis or extraction and the identification of its biological targets and mechanisms of action. Future trends and prospects in the application of 8-Ethoxy-9-ethyl-9H-purin-6-amine in scientific research include its potential use as a chemotherapeutic agent and its role in pollution management and sustainability.

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