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3-(4-Chlorbutyl)-1H-indol-5-carbonitril CAS:143612-79-7

3-(4-Chlorobutyl)-1H-indol-5-carbonitrile is an indole derivative characterized by a unique combination of indole and nitrile functional groups, along with a chlorobutyl side chain. This compound has gained attention in the field of medicinal chemistry due to its potential biological activities, which may include antimicrobial, anti-inflammatory, and anticancer properties. The indole scaffold serves as a versatile backbone for designing pharmaceuticals, while the presence of the chlorobutyl group enhances its lipophilicity, potentially improving bioavailability. Ongoing research aims to explore the therapeutic applications and mechanisms of action associated with this compound.


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Application and Effect:

3-(4-Chlorbutyl)-1H-indol-5-carbonitrile is a synthetic compound that has emerged as a subject of interest in medicinal chemistry due to its complex structure and potential pharmacological properties. The indole ring system is a well-established pharmacophore known for its broad spectrum of biological activities, including antitumor, antidepressant, and anti-inflammatory effects. By introducing a carbonitrile group at the 5-position and a 4-chlorobutyl substituent, researchers have aimed to enhance the activity and selectivity of the compound against specific biological targets. The synthesis of 3-(4-Chlorbutyl)-1H-indol-5-carbonitrile typically involves multi-step organic reactions, including the formation of the indole core followed by the introduction of the chlorobutyl and nitrile functionalities. The presence of the chlorobutyl group not only influences the compound's solubility and lipophilicity but also plays a crucial role in modulating its interaction with biological targets, which can lead to improved efficacy compared to other indole derivatives lacking such substituents. Preliminary biological studies suggest that compounds of this nature may possess significant antibacterial or anti-inflammatory properties, making them candidates for further development in therapeutic applications. Investigations into the compound's mechanism of action are essential for understanding how it interacts with cellular pathways and contributes to its biological effects. Additionally, structure-activity relationship (SAR) studies could reveal modifications that enhance potency and selectivity. Furthermore, the exploration of 3-(4-Chlorbutyl)-1H-indol-5-carbonitrile in drug discovery aligns with the broader objective of identifying new agents to combat various diseases, particularly those resistant to existing treatments. As such, ongoing research endeavors continue to shed light on the potential utility of this compound in addressing unmet medical needs, underscoring its relevance in contemporary pharmaceutical science. Overall, 3-(4-Chlorbutyl)-1H-indol-5-carbonitrile embodies the innovative approaches being employed in the search for novel therapeutic agents derived from indole-based frameworks.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C13H13ClN2
Assay 99%
Appearance white powder
CAS No.  143612-79-7
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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