Date published: 2026-2-2

1-800-457-3801

SCBT Portrait Logo
Seach Input

SR-1F Activators

SR-1F Activators belong to a distinctive chemical class known for their potent modulatory effects on specific biological processes within the body. These compounds are characterized by their unique chemical structure and their ability to interact with specific molecular targets, eliciting a cascade of cellular responses. SR-1F Activators are synthetic small molecules designed with precision to engage with a particular subset of receptors and signaling pathways in living organisms. The nomenclature "SR-1F" signifies their specific molecular profile, which is essential for their targeted actions. At the molecular level, SR-1F Activators are typically composed of a core scaffold with various functional groups strategically positioned to facilitate interactions with their intended targets. These compounds often exhibit a high degree of selectivity, binding to and influencing the activity of specific proteins or enzymes involved in crucial cellular processes. Their mechanism of action can vary widely, but the common goal is to modulate cellular responses by either enhancing or inhibiting the function of the target molecules. Researchers have harnessed the potential of SR-1F Activators to gain insights into the underlying mechanisms of cellular regulation and to explore the intricacies of signal transduction pathways.

Items 1 to 10 of 15 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

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)

Binds to retinoic acid receptors and activates SR-1F gene

LY 344864 hydrochloride

186544-26-3sc-361245
sc-361245A
10 mg
50 mg
$179.00
$739.00
(0)

LY 344864 hydrochloride, acting as an SR-1F, exhibits distinctive reactivity patterns due to its unique electronic structure. The compound engages in selective nucleophilic attacks, leading to the formation of stable intermediates. Its propensity for intramolecular interactions enhances reaction kinetics, allowing for rapid transformations. Additionally, the presence of halide ions influences solvation dynamics, affecting its behavior in various chemical environments and contributing to its versatility in synthetic chemistry.

LY 334370 hydrochloride

182563-08-2sc-361243
sc-361243A
5 mg
25 mg
$95.00
$384.00
(0)

LY 334370 hydrochloride, functioning as an SR-1F, showcases remarkable selectivity in its reactivity, primarily driven by its unique steric and electronic properties. This compound facilitates specific electrophilic interactions, promoting the formation of transient species that can undergo rapid rearrangements. Its ability to stabilize charged intermediates through hydrogen bonding enhances its reactivity profile, while the halide component modulates its solubility and reactivity in diverse solvent systems, making it a versatile agent in chemical synthesis.

(−)-Epigallocatechin Gallate

989-51-5sc-200802
sc-200802A
sc-200802B
sc-200802C
sc-200802D
sc-200802E
10 mg
50 mg
100 mg
500 mg
1 g
10 g
$43.00
$73.00
$126.00
$243.00
$530.00
$1259.00
11
(1)

Modulates various signaling pathways promoting SR-1F

BRL 54443 maleate salt

1197333-54-2sc-300302
10 mg
$118.00
(0)

BRL 54443 maleate salt, functioning as an SR-1F, showcases remarkable interaction dynamics attributed to its specific stereochemistry and functional groups. The compound facilitates unique hydrogen bonding and dipole-dipole interactions, which enhance its solubility in diverse solvents. Its reactivity is characterized by rapid acyl transfer processes, allowing for efficient formation of reactive species. Additionally, the presence of the maleate moiety contributes to its distinct conformational flexibility, influencing reaction pathways and kinetics.

BRL 54443

57477-39-1sc-203855
sc-203855A
10 mg
50 mg
$118.00
$465.00
(1)

BRL 54443, acting as an SR-1F, exhibits distinctive reactivity patterns due to its unique electronic configuration and steric hindrance. This compound engages in selective nucleophilic attacks, leading to the formation of stable intermediates that can participate in further transformations. Its acid halide nature allows for efficient acylation reactions, while the halogen substituent influences its reactivity and solubility across various polar and non-polar environments, enhancing its utility in synthetic applications.

Zolmitriptan-D6 (Major)

1217644-84-2sc-220416
1 mg
$490.00
(0)

Zolmitriptan-D6 (Major), acting as an SR-1F, exhibits intriguing molecular behavior due to its isotopic labeling, which alters its vibrational spectra and reaction kinetics. The compound engages in selective hydrogen bonding and exhibits unique steric effects that influence its interaction with various substrates. Its distinct electronic properties enhance reactivity, facilitating specific pathways in acylation reactions. The isotopic substitution also provides insights into mechanistic studies through kinetic isotope effects, revealing deeper understanding of its chemical reactivity.

Valproic Acid

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

Histone deacetylase inhibitor, epigenetic regulation

5-Azacytidine

320-67-2sc-221003
500 mg
$280.00
4
(1)

DNA demethylating agent, activates SR-1F transcription

D,L-Sulforaphane

4478-93-7sc-207495A
sc-207495B
sc-207495C
sc-207495
sc-207495E
sc-207495D
5 mg
10 mg
25 mg
1 g
10 g
250 mg
$153.00
$292.00
$489.00
$1325.00
$8465.00
$933.00
22
(1)

Induces antioxidant response, upregulates SR-1F