7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione - 389614-94-2

7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione

Catalog Number: EVT-254826
CAS Number: 389614-94-2
Molecular Formula: C19H17ClN2O2
Molecular Weight: 340.8 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.

Product Introduction

Description
7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione, also known as Cisplatin, is a chemotherapy drug used to treat various types of cancer. It was first synthesized in the 1960s and has since become a widely used drug in cancer treatment. This paper will discuss the method of synthesis or extraction, chemical structure and biological activity, biological effects, applications, and future perspectives and challenges of Cisplatin.
Applications in Various Fields
7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione has been used in medical research for its role in drug development and clinical trials. It has been shown to be effective in treating various types of cancer, and ongoing research is exploring its potential use in combination with other drugs. In environmental research, 7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione has been studied for its effects on ecosystems and its role in pollution management. In industrial research, it has been used in manufacturing processes to improve product quality and efficiency, with health and safety considerations being a top priority.

Properties

CAS Number

389614-94-2

Product Name

7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione

IUPAC Name

7-chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione

Molecular Formula

C19H17ClN2O2

Molecular Weight

340.8 g/mol

InChI

InChI=1S/C19H17ClN2O2/c1-3-22(4-2)13-9-7-12(8-10-13)15-16(20)19(24)17-14(18(15)23)6-5-11-21-17/h5-11H,3-4H2,1-2H3

InChI Key

XAZVKSMDPVMMPP-UHFFFAOYSA-N

SMILES

CCN(CC)C1=CC=C(C=C1)C2=C(C(=O)C3=C(C2=O)C=CC=N3)Cl

Synonyms

7-chloro-6-[4-(diethylamino)phenyl]-5,8-quinolinedione

Canonical SMILES

CCN(CC)C1=CC=C(C=C1)C2=C(C(=O)C3=C(C2=O)C=CC=N3)Cl
Method of Synthesis or Extraction
7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione is commonly synthesized through a reaction between cis-diammineplatinum(II) dichloride and silver nitrate. This method has a high yield and efficiency, with a purity of over 99%. However, it also has environmental and safety considerations, as it involves the use of toxic chemicals and generates hazardous waste.
Another method of synthesis is through the reaction between platinum(IV) chloride and ammonium chloride. This method has a lower yield and efficiency compared to the first method, but it is less hazardous and more environmentally friendly.
Chemical Structure and Biological Activity
7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione has a unique chemical structure, consisting of a platinum atom surrounded by two chloride ions and two ammonia molecules. It works by binding to DNA and preventing cell division, ultimately leading to cell death. 7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione has been shown to be effective against a variety of cancers, including testicular, ovarian, bladder, and lung cancer.
Biological Effects
7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione has both therapeutic and toxic effects on the body. Its therapeutic effects include its ability to inhibit cancer cell growth and induce apoptosis. However, it can also cause side effects such as nausea, vomiting, and kidney damage. 7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione has also been shown to affect cell function and signal transduction, leading to changes in gene expression and protein synthesis.
Future Perspectives and Challenges
One of the current limitations in the use and study of 7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione is its toxicity and potential side effects. Researchers are exploring ways to reduce these side effects while maintaining its effectiveness as a cancer treatment. Possible solutions include developing new drug delivery methods or combining 7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione with other drugs to reduce toxicity. Future trends and prospects in the application of 7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione in scientific research include its potential use in personalized medicine and the development of new cancer treatments.
Conclusion:
7-Chloro-6-[4-(diethylamino)phenyl]quinoline-5,8-dione is a widely used chemotherapy drug with a unique chemical structure and mechanism of action. Its effectiveness in treating various types of cancer has made it an important tool in medical research. However, its potential side effects and environmental and safety considerations highlight the need for ongoing research and development to improve its use and study.

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