Date published: 2025-12-6

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AR Activators

Santa Cruz Biotechnology now offers a broad range of AR Activators for use in various applications. AR activators, or Androgen Receptor activators, are a crucial category of chemicals used extensively in scientific research to explore the intricate mechanisms of androgen signaling, which plays a vital role in various physiological processes including development, metabolism, and reproduction. The androgen receptor (AR) is a type of nuclear receptor that is activated by binding to androgens, such as testosterone and dihydrotestosterone, leading to the regulation of gene expression that affects cellular growth and differentiation. By utilizing AR activators, researchers can study the precise activation and modulation of this receptor, providing valuable insights into its role in cell signaling and gene regulation. These activators are indispensable in experiments aimed at understanding how androgen signaling influences developmental processes, tissue homeostasis, and metabolic pathways. Moreover, AR activators are used to investigate the receptor's involvement in diverse biological systems, including the musculoskeletal system, where they regulate muscle and bone development, and the nervous system, where they influence neural differentiation and function. In the field of endocrinology, AR activators are employed to study the cross-talk between androgen signaling and other hormonal pathways, offering deeper insights into the complex regulatory networks that govern cellular function and organismal physiology. The availability of a wide range of AR activators allows researchers to tailor their experimental approaches to specific aspects of androgen receptor function, thereby advancing our understanding of this critical signaling pathway. View detailed information on our available AR Activators by clicking on the product name.

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Items 31 to 34 of 34 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Tetrahydrozoline-d4 Hydrochloride

sc-220222
1 mg
$330.00
(0)

Tetrahydrozoline-d4 Hydrochloride exhibits notable behavior as an acid halide, characterized by its enhanced reactivity due to deuteration. This modification influences its electronic properties, allowing for selective interactions with nucleophiles. The compound's unique steric configuration promotes distinct reaction pathways, resulting in varied kinetics. Additionally, its solubility and stability in various solvents facilitate innovative synthetic routes, enabling the exploration of novel derivatives with tailored functionalities.

Dihydroergotamine (+)-tartrate salt

5989-77-5sc-263091A
sc-263091
50 mg
100 mg
$338.00
$678.00
(0)

Dihydroergotamine (+)-tartrate salt demonstrates intriguing behavior as an acid halide, primarily through its ability to form stable complexes with metal ions, which can alter its reactivity profile. The presence of multiple functional groups allows for diverse intermolecular interactions, enhancing its potential for catalysis. Its unique stereochemistry influences reaction dynamics, leading to selective pathways that can be exploited in synthetic chemistry. Furthermore, its solubility characteristics enable effective manipulation in various reaction environments.

(±)-Epinephrine hydrochloride

329-63-5sc-252780
sc-252780A
sc-252780B
5 g
25 g
1 kg
$82.00
$337.00
$7140.00
1
(1)

(±)-Epinephrine hydrochloride exhibits distinctive behavior as an acid halide, characterized by its capacity to engage in hydrogen bonding and ionic interactions, which significantly influence its reactivity. The compound's chiral centers contribute to its stereospecific interactions, allowing for selective binding to various substrates. Additionally, its solubility in polar solvents facilitates rapid diffusion and reaction kinetics, making it a versatile participant in complex chemical systems.

Isoetharine mesylate salt

7279-75-6sc-252918
1 g
$66.00
(0)

Isoetharine mesylate salt demonstrates unique reactivity as an acid halide, primarily through its ability to form stable complexes with nucleophiles due to its electrophilic nature. The presence of the mesylate group enhances its solubility in polar environments, promoting efficient molecular interactions. Its distinct steric configuration allows for selective reactivity pathways, influencing the kinetics of reactions and enabling it to participate in diverse chemical transformations with precision.