Date published: 2026-4-1

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Gpr165 Activators

The chemical class known as Gpr165 Activators encompasses a range of compounds specifically designed to enhance or stimulate the activity of the Gpr165 protein. Gpr165, identified through extensive molecular and genomic research, is a G-protein coupled receptor (GPCR) known to play a critical role in a variety of cellular processes. The functionality of Gpr165 is essential in cellular signaling pathways, where it acts as a mediator for various biological responses. The activators targeting Gpr165 are developed with the objective of binding to this receptor and promoting its activity. This activation is crucial as it facilitates the receptor's ability to transmit signals, thereby influencing the biochemical pathways in which Gpr165 is involved. By stimulating the activity of Gpr165, these activators are designed to amplify the associated cellular processes, potentially affecting specific cellular functions and mechanisms.

The development of Gpr165 Activators is a complex and interdisciplinary endeavor, involving the integration of molecular biology, medicinal chemistry, and pharmacology. The initial phase of this development process involves attaining a deep understanding of the structure and function of the Gpr165 protein. Advanced techniques such as X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, and computational molecular modeling are utilized to gain a detailed perspective of the receptor. This foundational knowledge is critical for the rational design of activators that are effective in their interaction with Gpr165 and exhibit a high degree of specificity. Typically, these activators are small molecules or peptides, designed to efficiently interact with the receptor and induce its activation. The molecular design of these activators is carefully optimized to ensure robust interactions with Gpr165, often involving specific binding sites and conformational changes that trigger receptor activation. The efficacy of these activators is evaluated through various biochemical and cellular assays in vitro and in cellular models. These assays are essential for determining the activators' potency, specificity, and overall impact on Gpr165 signaling pathways, providing key insights into their behavior and mechanism of action. Such research is fundamental for understanding the potential of Gpr165 Activators in modulating cellular processes and for further exploration into their implications in cellular signaling and function.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Aza-2′-Deoxycytidine

2353-33-5sc-202424
sc-202424A
sc-202424B
25 mg
100 mg
250 mg
$218.00
$322.00
$426.00
7
(1)

This compound is a DNA methyltransferase inhibitor that may lead to the demethylation of gene promoters, potentially resulting in gene activation.

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$152.00
$479.00
$632.00
$1223.00
$2132.00
33
(3)

Trichostatin A is a histone deacetylase inhibitor that can lead to a more open chromatin structure, potentially increasing gene transcription.

Retinoic Acid, all trans

302-79-4sc-200898
sc-200898A
sc-200898B
sc-200898C
500 mg
5 g
10 g
100 g
$66.00
$325.00
$587.00
$1018.00
28
(1)

Retinoic acid can modulate gene expression by activating retinoic acid receptors, which act as transcription factors for various genes.

PMA

16561-29-8sc-3576
sc-3576A
sc-3576B
sc-3576C
sc-3576D
1 mg
5 mg
10 mg
25 mg
100 mg
$41.00
$132.00
$214.00
$500.00
$948.00
119
(6)

PMA activates protein kinase C, which can lead to the activation of downstream signaling pathways affecting gene expression.

Sodium Butyrate

156-54-7sc-202341
sc-202341B
sc-202341A
sc-202341C
250 mg
5 g
25 g
500 g
$31.00
$47.00
$84.00
$222.00
19
(3)

Sodium butyrate is a histone deacetylase inhibitor that can increase histone acetylation, potentially enhancing gene expression.

Valproic Acid

99-66-1sc-213144
10 g
$87.00
9
(1)

Valproic Acid is another histone deacetylase inhibitor that may lead to chromatin remodeling and activation of some genes.

Theophylline

58-55-9sc-202835
sc-202835A
sc-202835B
5 g
25 g
100 g
$20.00
$32.00
$85.00
6
(0)

Theophylline is a phosphodiesterase inhibitor that may lead to increased cAMP levels, potentially affecting gene transcription.

β-Estradiol

50-28-2sc-204431
sc-204431A
500 mg
5 g
$63.00
$182.00
8
(1)

β-estradiol binds to estrogen receptors, which may regulate gene transcription upon binding to DNA response elements.

Lithium

7439-93-2sc-252954
50 g
$214.00
(0)

Lithium chloride can inhibit GSK-3, potentially leading to the activation of Wnt signaling and affecting gene expression.

17-AAG

75747-14-7sc-200641
sc-200641A
1 mg
5 mg
$67.00
$156.00
16
(2)

17-AAG interferes with Hsp90’s chaperone function, which may lead to the destabilization of client proteins and alter gene expression.