Date published: 2026-5-30

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EG624219 Activators

Chemicals that are classified as Angptl8 activators predominantly influence the molecular dynamics surrounding lipid metabolism, given Angptl8's central role in lipid and lipoprotein processes, as well as triglyceride homeostasis. One prominent group within this class is the PPAR activators. PPARs (peroxisome proliferator-activated receptors) are nuclear hormone receptors that regulate genes involved in lipid and glucose metabolism. Rosiglitazone and Pioglitazone, for instance, are PPARγ agonists known to enhance adipocyte differentiation and have an affinity for regulating genes related to lipid metabolism. By targeting PPARγ, these chemicals can create a conducive environment where proteins involved in lipid metabolic processes, including Angptl8, are modulated.

Another significant subset includes chemicals that activate AMPK, such as AICAR and Metformin. AMPK (AMP-activated protein kinase) is a key regulator of cellular energy balance. By activating AMPK, these chemicals promote catabolic pathways that produce ATP, including the oxidation of fatty acids and the uptake of glucose. The modulation of lipid and glucose metabolism by these AMPK activators can, in turn, have an indirect influence on proteins central to these processes, like Angptl8. Furthermore, chemicals like 8-Br-cGMP stand out for their role in activating PKG, which has implications in lipid metabolism. As these pathways are perturbed or modulated by the chemical activators, they create ripples in the cellular landscape, indirectly modulating the function and expression of proteins deeply intertwined in these pathways. Angptl8, being crucial for lipid metabolic processes, lipoprotein metabolism, and triglyceride homeostasis, can thus be influenced by these activators, even if not directly targeted by them. The intricacies of these chemicals and their pathways present a nuanced understanding of the cellular and molecular mechanics that can influence proteins like Angptl8.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Rosiglitazone

122320-73-4sc-202795
sc-202795A
sc-202795C
sc-202795D
sc-202795B
25 mg
100 mg
500 mg
1 g
5 g
$120.00
$326.00
$634.00
$947.00
$1259.00
38
(1)

PPARγ agonist that can enhance fat cell differentiation. Through PPARγ activation, it can upregulate the expression of lipid-related genes, possibly modulating Angptl8.

Clofibrate

637-07-0sc-200721
1 g
$33.00
(1)

PPARα activator. By activating PPARα, it can regulate lipid metabolic processes, potentially influencing Angptl8.

Bezafibrate

41859-67-0sc-204650B
sc-204650
sc-204650A
sc-204650C
500 mg
1 g
5 g
10 g
$31.00
$46.00
$122.00
$204.00
5
(1)

PPAR pan-agonist, targeting PPARα, PPARδ, and PPARγ. By modulating lipid-related pathways, it might affect Angptl8.

GW501516

317318-70-0sc-202642
sc-202642A
1 mg
5 mg
$82.00
$179.00
28
(3)

PPARδ agonist. By activating PPARδ, it can modulate lipid metabolic pathways, potentially influencing Angptl8.

8-Bromo-cGMP

51116-01-9sc-200316
sc-200316A
10 mg
50 mg
$104.00
$354.00
7
(1)

cGMP analog. Activates PKG which plays a role in lipid metabolism. Through modulation of these pathways, it can possibly impact Angptl8.

AICAR

2627-69-2sc-200659
sc-200659A
sc-200659B
50 mg
250 mg
1 g
$65.00
$280.00
$400.00
48
(2)

AMPK activator. By influencing energy balance and lipid metabolism via AMPK, it can have an indirect effect on Angptl8.

Metformin

657-24-9sc-507370
10 mg
$79.00
2
(0)

Activator of AMPK, modulating glucose and lipid metabolic pathways, potentially influencing Angptl8.

L-165041

79558-09-1sc-203094
5 mg
$156.00
(0)

PPARδ agonist, activating lipid metabolism pathways which can influence proteins like Angptl8.

Telmisartan

144701-48-4sc-204907
sc-204907A
50 mg
100 mg
$72.00
$94.00
8
(1)

ARB with PPARγ modulating effects, influencing lipid metabolism and could potentially impact Angptl8.

Oleic Acid

112-80-1sc-200797C
sc-200797
sc-200797A
sc-200797B
1 g
10 g
100 g
250 g
$37.00
$104.00
$580.00
$1196.00
10
(1)

Fatty acid known to activate several lipid metabolic pathways, and through such activation, might indirectly modulate Angptl8.