Date published: 2026-4-26

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SR-A Inhibitors

SR-A inhibitors belong to a distinctive chemical class of compounds designed to modulate the activity of Scavenger Receptor Class A (SR-A). SR-A is a type of cell surface receptor predominantly found on macrophages and other immune cells, and it plays a pivotal role in the innate immune response. These inhibitors are synthesized with the primary objective of regulating the function of SR-A and influencing cellular processes that are mediated by this receptor.

The chemical structure of SR-A inhibitors typically comprises a diverse range of organic molecules that exhibit specific binding affinities for SR-A. These compounds are carefully designed to interact with the receptor's ligand-binding domains, thereby preventing its engagement with its natural ligands. This interference can lead to a cascade of downstream effects, including the attenuation of phagocytosis and cytokine production. By modulating SR-A activity, these inhibitors hold the ability to impact various immune responses and inflammatory pathways, making them valuable tools for researchers exploring the intricate mechanisms of innate immunity and inflammation. Understanding the structural properties and binding affinities of SR-A inhibitors is crucial for elucidating their precise modes of action and applications in a variety of research contexts, such as immunology, cell biology, and molecular pharmacology.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Aspirin

50-78-2sc-202471
sc-202471A
5 g
50 g
$20.00
$42.00
4
(1)

Acetylsalicylic acid, commonly known as aspirin, inhibits SR-A by blocking the activation of NF-κB, thus reducing inflammation and scavenger receptor expression.

Simvastatin

79902-63-9sc-200829
sc-200829A
sc-200829B
sc-200829C
50 mg
250 mg
1 g
5 g
$31.00
$89.00
$135.00
$443.00
13
(1)

Simvastatin lowers SR-A expression by inhibiting the mevalonate pathway, leading to decreased cholesterol synthesis and reduced atherogenic lipid uptake by macrophages.

Resveratrol

501-36-0sc-200808
sc-200808A
sc-200808B
100 mg
500 mg
5 g
$80.00
$220.00
$460.00
64
(2)

Resveratrol modulates SR-A activity through anti-inflammatory and antioxidant effects, reducing oxidative stress and inflammation in macrophages.

Cilostazol

73963-72-1sc-201182
sc-201182A
10 mg
50 mg
$109.00
$322.00
3
(1)

Cilostazol inhibits SR-A expression and activity by suppressing proinflammatory signaling pathways, including NF-κB, in macrophages.

Raloxifene

84449-90-1sc-476458
1 g
$802.00
3
(0)

Raloxifene reduces SR-A-mediated foam cell formation by modulating estrogen receptors and downstream signaling pathways involved in lipid metabolism and inflammation.

Troglitazone

97322-87-7sc-200904
sc-200904B
sc-200904A
5 mg
10 mg
25 mg
$110.00
$204.00
$435.00
9
(1)

Troglitazone, a PPAR-γ agonist, decreases SR-A expression by regulating lipid metabolism, insulin sensitivity, and inflammation in macrophages.

Apigenin

520-36-5sc-3529
sc-3529A
sc-3529B
sc-3529C
sc-3529D
sc-3529E
sc-3529F
5 mg
100 mg
1 g
5 g
25 g
100 g
1 kg
$33.00
$214.00
$734.00
$1151.00
$2348.00
$3127.00
$5208.00
22
(1)

Apigenin inhibits SR-A expression and activity by downregulating NF-κB and MAPK pathways, resulting in reduced inflammation and oxidative stress in macrophages.

Fenofibrate

49562-28-9sc-204751
5 g
$41.00
9
(1)

Fenofibrate, a PPAR-α agonist, decreases SR-A expression by enhancing lipid catabolism and reducing lipid accumulation, leading to reduced foam cell formation.

Luteolin

491-70-3sc-203119
sc-203119A
sc-203119B
sc-203119C
sc-203119D
5 mg
50 mg
500 mg
5 g
500 g
$27.00
$51.00
$101.00
$153.00
$1925.00
40
(1)

Luteolin inhibits SR-A through its antioxidant and anti-inflammatory properties, reducing macrophage activation and foam cell formation by scavenging reactive oxygen species.

Curcumin

458-37-7sc-200509
sc-200509A
sc-200509B
sc-200509C
sc-200509D
sc-200509F
sc-200509E
1 g
5 g
25 g
100 g
250 g
1 kg
2.5 kg
$37.00
$69.00
$109.00
$218.00
$239.00
$879.00
$1968.00
47
(1)

Curcumin inhibits SR-A expression by suppressing NF-κB activation and proinflammatory cytokine production in macrophages, mitigating atherosclerosis-related inflammation.