(Z)-FeCP-oxindole - 1137967-28-2
(Z)-FeCP-oxindole
Catalog Number: BT-254438
CAS Number: 1137967-28-2
Molecular Formula: C19H15FeNO
Molecular Weight: 329.18
The product is for non-human research only. Not for therapeutic or veterinary use.
Product Introduction
Description
(Z)-FeCP-oxindole is a chemical compound that has gained significant attention in the scientific community due to its potential therapeutic and environmental applications. It is a derivative of oxindole, a heterocyclic organic compound that is widely used in medicinal chemistry. (Z)-FeCP-oxindole has been found to exhibit potent biological activity, making it a promising candidate for drug development and environmental management.
Properties
CAS Number
1137967-28-2
Product Name
(Z)-FeCP-oxindole
IUPAC Name
cyclopenta-1,3-diene;3-(cyclopenta-2,4-dien-1-ylidenemethyl)-1H-indol-2-olate;iron(2+)
Molecular Formula
C19H15FeNO
Molecular Weight
329.18
InChI
InChI=1S/C14H11NO.C5H5.Fe/c16-14-12(9-10-5-1-2-6-10)11-7-3-4-8-13(11)15-14;1-2-4-5-3-1;/h1-9,15-16H;1-5H;/q;-1;+2/p-1
InChI Key
MTGBTDOTYGXLBK-UHFFFAOYSA-M
SMILES
[CH-]1C=CC=C1.C1=CC=C2C(=C1)C(=C(N2)[O-])C=C3C=CC=C3.[Fe+2]
Synonyms
(Z)-3-Ferrocenylmethylidene-1,3-dihydro-2H-indol-2-one
Method of Synthesis or Extraction
(Z)-FeCP-oxindole can be synthesized using various methods, including the Suzuki-Miyaura coupling reaction, the Heck reaction, and the Sonogashira coupling reaction. The Suzuki-Miyaura coupling reaction is the most commonly used method for the synthesis of (Z)-FeCP-oxindole. This method involves the reaction of an aryl halide with an organoboron compound in the presence of a palladium catalyst. The efficiency and yield of this method depend on the reaction conditions, such as the choice of solvent, temperature, and catalyst. The yield of (Z)-FeCP-oxindole using the Suzuki-Miyaura coupling reaction ranges from 50% to 90%. The environmental and safety considerations associated with this method include the use of toxic solvents and catalysts, which can lead to environmental pollution and health hazards.
Chemical Structure and Biological Activity
(Z)-FeCP-oxindole has a unique chemical structure that consists of a FeCP moiety and an oxindole ring. The FeCP moiety is a metal complex that contains iron and a chiral ligand, while the oxindole ring is a heterocyclic aromatic compound. The biological activity of (Z)-FeCP-oxindole is attributed to its ability to interact with biological targets, such as enzymes and receptors. The mechanism of action of (Z)-FeCP-oxindole involves the inhibition of enzyme activity or the modulation of receptor signaling pathways. (Z)-FeCP-oxindole has been found to exhibit potent bioactivity against various diseases, including cancer, inflammation, and neurodegenerative disorders. The potency of (Z)-FeCP-oxindole depends on the chemical structure, stereochemistry, and biological target.
Biological Effects
The biological effects of (Z)-FeCP-oxindole on cell function and signal transduction are diverse and complex. (Z)-FeCP-oxindole has been found to induce cell death, inhibit cell proliferation, and modulate cell differentiation. The potential therapeutic effects of (Z)-FeCP-oxindole include the treatment of cancer, inflammation, and neurodegenerative disorders. However, (Z)-FeCP-oxindole may also have toxic effects on cells, leading to adverse health outcomes. The potential toxic effects of (Z)-FeCP-oxindole include oxidative stress, DNA damage, and mitochondrial dysfunction.
Applications
(Z)-FeCP-oxindole has various applications in medical research, environmental research, and industrial research. In medical research, (Z)-FeCP-oxindole has been studied for its role in drug development, clinical trials, and findings. The benefits of (Z)-FeCP-oxindole in medical research include its potent bioactivity and potential therapeutic effects. However, the potential side effects of (Z)-FeCP-oxindole must also be considered. In environmental research, (Z)-FeCP-oxindole has been studied for its effects on ecosystems, role in pollution management, and sustainability and environmental impact. The benefits of (Z)-FeCP-oxindole in environmental research include its ability to degrade pollutants and improve environmental sustainability. In industrial research, (Z)-FeCP-oxindole has been studied for its use in manufacturing processes, improving product quality and efficiency, and health and safety considerations.
Future Perspectives and Challenges
The current limitations in the use and study of (Z)-FeCP-oxindole include the lack of understanding of its mechanism of action, potential toxic effects, and environmental impact. Possible solutions and improvements include the development of new synthesis methods, the identification of new biological targets, and the evaluation of its environmental impact. Future trends and prospects in the application of (Z)-FeCP-oxindole in scientific research include the development of new drugs, the improvement of environmental sustainability, and the advancement of industrial processes.
Conclusion:
(Z)-FeCP-oxindole is a promising chemical compound that has potential applications in various fields, including medical research, environmental research, and industrial research. The method of synthesis or extraction, chemical structure, biological activity, biological effects, applications, future perspectives, and challenges associated with (Z)-FeCP-oxindole have been discussed in this paper. Further research is needed to fully understand the potential of (Z)-FeCP-oxindole and its impact on human health and the environment.
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