Date published: 2026-4-26

1-800-457-3801

SCBT Portrait Logo
Seach Input

Flt Inhibitors

Santa Cruz Biotechnology now offers a broad range of Flt Inhibitors for use in various applications. Flt Inhibitors are a vital category of biochemical tools utilized extensively in scientific research, particularly in the fields of molecular biology, biochemistry, and cell biology. Flt, a family of receptor tyrosine kinases, plays a crucial role in cellular processes such as signal transduction, cell differentiation, and growth. By inhibiting Flt activity, researchers can dissect the intricate pathways involved in cell signaling and understand the regulatory mechanisms governing these processes. Flt Inhibitors are indispensable for studying the specific interactions and signaling cascades mediated by Flt receptors, providing insights into how cells respond to external stimuli and regulate their behavior. These inhibitors are essential for exploring the molecular underpinnings of cell communication and the dynamic processes of cellular adaptation and response. In experimental settings, Flt Inhibitors allow for precise manipulation of kinase activity, facilitating detailed investigations into enzyme kinetics, substrate specificity, and the broader implications of altered Flt signaling on cellular functions. Additionally, these inhibitors are valuable in structural biology for explaining the three-dimensional configurations of Flt receptors and their complexes, revealing critical information about their functional domains and interaction sites. This comprehensive understanding is fundamental for advancing our knowledge of cellular signaling networks and the intricate balance of cellular activities. Flt Inhibitors thus serve as crucial tools for researchers aiming to uncover the complexities of cellular communication and regulation. View detailed information on our available Flt Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

VEGFR Tyrosine Kinase Inhibitor II

269390-69-4sc-204378
5 mg
$212.00
1
(0)

VEGFR Tyrosine Kinase Inhibitor II exhibits a selective interaction with the Flt receptor, characterized by its ability to disrupt ATP binding through competitive inhibition. This compound's unique structural features allow for specific electrostatic interactions with charged residues, modulating the receptor's kinase activity. Its conformational flexibility enables dynamic adjustments during binding, influencing the overall reaction kinetics and enhancing its inhibitory efficacy within cellular signaling networks.

VEGFR Tyrosine Kinase Inhibitor V

861874-34-2 anhydroussc-356190
5 mg
$240.00
(0)

VEGFR Tyrosine Kinase Inhibitor V demonstrates a remarkable affinity for the Flt receptor, engaging in allosteric modulation that alters the receptor's conformation. This compound's unique hydrophobic regions facilitate critical van der Waals interactions, enhancing binding stability. Its kinetic profile reveals a slow dissociation rate, allowing prolonged receptor occupancy. Additionally, the compound's solubility characteristics promote effective distribution within cellular environments, impacting downstream signaling pathways.

AP 24534 HCl

943319-70-8 free basesc-396905
sc-396905A
10 mg
50 mg
$112.00
$138.00
(0)

AP 24534 HCl exhibits a distinctive interaction with the Flt receptor through a dual binding mechanism that stabilizes its active conformation. The presence of polar functional groups enhances hydrogen bonding, contributing to its selectivity. Its reaction kinetics are characterized by a rapid association phase, followed by a gradual equilibrium, which allows for sustained receptor engagement. Furthermore, the compound's unique solvation dynamics facilitate efficient cellular uptake, influencing various signaling cascades.