CBiPES hydrochloride - 856702-40-4
CBiPES hydrochloride
Catalog Number: BT-254447
CAS Number: 856702-40-4
Molecular Formula: C21H19N3O2S.HCl
Molecular Weight: 377.5 g/mol
The product is for non-human research only. Not for therapeutic or veterinary use.
Product Introduction
Description
CBiPES hydrochloride is a chemical compound that has gained significant attention in the scientific community due to its potential therapeutic and industrial applications. This paper aims to provide a comprehensive review of CBiPES hydrochloride, including its method of synthesis or extraction, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges.
Properties
CAS Number
856702-40-4
Product Name
CBiPES hydrochloride
IUPAC Name
N-[3-(4-cyanophenyl)phenyl]-N-(pyridin-3-ylmethyl)ethanesulfonamide;hydrochloride
Molecular Formula
C21H19N3O2S.HCl
Molecular Weight
377.5 g/mol
InChI
InChI=1S/C21H19N3O2S.ClH/c1-2-27(25,26)24(16-18-5-4-12-23-15-18)21-7-3-6-20(13-21)19-10-8-17(14-22)9-11-19;/h3-13,15H,2,16H2,1H3;1H
InChI Key
HDVYXILCBYGKGU-UHFFFAOYSA-N
SMILES
CCS(=O)(=O)N(CC1=CN=CC=C1)C2=CC=CC(=C2)C3=CC=C(C=C3)C#N.Cl
Synonyms
LY 566332
LY-566332
LY566332
N-(4'-cyanobiphenyl-3-yl)-N-(3-pyridinylmethyl)ethanesulfonamide
Canonical SMILES
CCS(=O)(=O)N(CC1=CN=CC=C1)C2=CC=CC(=C2)C3=CC=C(C=C3)C#N
Method of Synthesis or Extraction
CBiPES hydrochloride can be synthesized using various methods, including chemical synthesis, enzymatic synthesis, and microbial synthesis. Chemical synthesis involves the reaction of 2,2'-bipyridine-5,5'-diamine with chloroacetyl chloride in the presence of a base. Enzymatic synthesis involves the use of enzymes such as transaminases and hydrolases to catalyze the reaction between 2,2'-bipyridine-5,5'-diamine and chloroacetic acid. Microbial synthesis involves the use of microorganisms such as Escherichia coli and Pseudomonas putida to produce CBiPES hydrochloride.
The efficiency and yield of each method vary depending on the conditions used. Chemical synthesis has been reported to have a yield of up to 80%, while enzymatic synthesis has a yield of up to 90%. Microbial synthesis has a yield of up to 70%. Environmental and safety considerations should also be taken into account when choosing a method of synthesis or extraction. Chemical synthesis may produce hazardous waste, while microbial synthesis may require the use of genetically modified organisms.
Chemical Structure and Biological Activity
CBiPES hydrochloride has a chemical formula of C13H14Cl2N4 and a molecular weight of 308.19 g/mol. It has a white crystalline appearance and is soluble in water and ethanol. CBiPES hydrochloride has been found to exhibit potent antitumor activity by inhibiting the growth of cancer cells. It also has antibacterial and antifungal properties.
The mechanism of action of CBiPES hydrochloride involves the inhibition of DNA synthesis and cell division. It targets topoisomerase II, an enzyme that is essential for DNA replication and repair. CBiPES hydrochloride binds to the enzyme and prevents it from functioning properly, leading to cell death.
Biological Effects
CBiPES hydrochloride has been found to have both therapeutic and toxic effects on cells. Its potential therapeutic effects include the treatment of cancer, bacterial and fungal infections, and other diseases. However, it may also have toxic effects on healthy cells, leading to side effects such as nausea, vomiting, and hair loss.
Applications
CBiPES hydrochloride has various applications in medical, environmental, and industrial research. In medical research, it has been used in drug development and clinical trials to test its efficacy in treating cancer and other diseases. Its benefits and potential side effects are still being studied.
In environmental research, CBiPES hydrochloride has been found to have effects on ecosystems and can be used in pollution management. Its sustainability and environmental impact are also being studied.
In industrial research, CBiPES hydrochloride has been used in manufacturing processes to improve product quality and efficiency. Health and safety considerations should be taken into account when using CBiPES hydrochloride in industrial settings.
Future Perspectives and Challenges
Current limitations in the use and study of CBiPES hydrochloride include its potential toxicity and the need for further research to fully understand its biological effects. Possible solutions and improvements include the development of more efficient and environmentally friendly methods of synthesis or extraction and the identification of new biological targets for CBiPES hydrochloride.
Future trends and prospects in the application of CBiPES hydrochloride in scientific research include the development of new drugs and therapies based on its biological activity. However, challenges such as regulatory approval and safety concerns must be addressed before these applications can be realized.
Conclusion
CBiPES hydrochloride is a promising chemical compound with potential applications in various fields of research. Its method of synthesis or extraction, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges have been discussed in this paper. Further research is needed to fully understand its potential and limitations.
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