Date published: 2025-12-24

1-800-457-3801

SCBT Portrait Logo
Seach Input

group IVD sPLA2 Inhibitors

Group IVD sPLA2 inhibitors belong to a chemically distinct class of compounds that are designed to interact with and inhibit the activity of the enzyme known as group IVD secretory phospholipase A2 (sPLA2). These inhibitors possess a unique molecular structure that enables them to specifically target and bind to the active site of the group IVD sPLA2 enzyme, thereby disrupting its normal function. By interfering with the enzymatic activity of group IVD sPLA2, these inhibitors have the potential to modulate various cellular and biochemical processes that are influenced by the release of arachidonic acid, a key intermediate in the lipid metabolism pathway. The structural features of group IVD sPLA2 inhibitors are designed to enable them to effectively bind to the active site of the enzyme. This binding interaction prevents the enzyme from catalyzing the hydrolysis of phospholipids, which is its natural function. By inhibiting this catalytic activity, these inhibitors disrupt the release of arachidonic acid from phospholipids, thereby interfering with downstream signaling pathways and cellular responses that rely on the availability of arachidonic acid. The unique chemical properties of group IVD sPLA2 inhibitors allow them to specifically target the group IVD sPLA2 enzyme, distinguishing them from other classes of sPLA2 inhibitors that may target different isoforms of the enzyme. This selectivity ensures that the inhibitors primarily interact with group IVD sPLA2, limiting their effects to the processes regulated by this specific enzyme.

Despite ongoing scientific investigation, the exact mechanisms and effects of group IVD sPLA2 inhibitors on cellular and biochemical processes are still being elucidated. Researchers are exploring the potential implications of inhibiting group IVD sPLA2 in various physiological contexts, seeking to uncover the full extent of their influence on cellular signaling, lipid metabolism, and other relevant pathways. The development and study of group IVD sPLA2 inhibitors offer promising avenues for further understanding the complex interplay between the enzyme and its biological functions, shedding light on the potential significance of targeting group IVD sPLA2.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Quinacrine, Dihydrochloride

69-05-6sc-204222
sc-204222B
sc-204222A
sc-204222C
sc-204222D
100 mg
1 g
5 g
200 g
300 g
$45.00
$56.00
$85.00
$3193.00
$4726.00
4
(2)

Originally developed as an antimalarial drug, quinacrine has also been found to inhibit PLA2 enzymes, including PLA2G4D.

MAFP

188404-10-6sc-203440
5 mg
$215.00
4
(1)

MAFP is a potent and irreversible inhibitor of PLA2 enzymes, including PLA2G4D. It covalently modifies the active site of the enzyme.

ONO-RS-082

99754-06-0sc-201410
sc-201410A
20 mg
100 mg
$81.00
$225.00
(1)

This compound is a selective inhibitor of cytosolic PLA2 enzymes, which may include PLA2G4D.

Neomycin sulfate

1405-10-3sc-3573
sc-3573A
1 g
5 g
$26.00
$34.00
20
(5)

While primarily known as an antibiotic, neomycin has been reported to inhibit PLA2 activity, including PLA2G4D.

Ibuprofen

15687-27-1sc-200534
sc-200534A
1 g
5 g
$52.00
$86.00
6
(0)

Ibuprofen, a nonsteroidal anti-inflammatory drug (NSAID), has been found to have inhibitory effects on PLA2 enzymes, including PLA2G4D.