44 Results for "

sPLA2

" in MedChemExpress (MCE) Product Catalog:
Products (44)

44 Results for "sPLA2" in MCE Product Catalog:

9
9 Publications Verification
Cat. No.: HY-13402
CAS No.: 172732-68-2
Purity:  99.23%
Synonyms: LY315920
Target:  

Phospholipase

Research Areas:  

Inflammation/Immunology

Varespladib (LY315920) is a potent and selective group IIA, secretory phospholipase A2 (sPLA2) inhibitor with an IC50 of 9 nM. Varespladib exhibits the significant inhibitory effect on sPLA2 activity in serum from various species including rat, rabbit, guinea pig and human with IC50s of 8.1 nM, 5.0 nM, 3.2 nM and 6.2 nM, respectively .
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9
9 Publications Verification
Cat. No.: HY-13402A
CAS No.: 172733-42-5
Purity:  ≥98.0%
Synonyms: LY315920 sodium
Target:  

Phospholipase

Research Areas:  

Inflammation/Immunology

Varespladib sodium (LY315920 sodium) is a potent and selective group IIA, secretory phospholipase A2 (sPLA2) inhibitor with an IC50 of 9 nM. Varespladib sodium exhibits the significant inhibitory effect on sPLA2 activity in serum from various species including rat, rabbit, guinea pig and human with IC50s of 8.1 nM, 5.0 nM, 3.2 nM and 6.2 nM, respectively .
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5
5 Cited Publications
Cat. No.: HY-N0134
CAS No.: 568-73-0
Synonyms: Tanshinone A
Tanshinone I is an inhibitor of type IIA human recombinant sPLA2 (IC50=11 μM) and rabbit recombinant cPLA2 (IC50=82 μM).
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3
3 Cited Publications
Cat. No.: HY-P74628
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: Phospholipase A2, membrane associated; EF; GIIC sPLA2
Species:  
Source:  
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1
1 Cited Publications
Cat. No.: HY-17485
CAS No.: 39718-89-3
Synonyms: EB-382
Target:  

Phospholipase COX

Research Areas:  

Inflammation/Immunology

Alminoprofen (EB-382) is a nonsteroidal anti-inflammatory agent (NSAID) of the phenylpropionic acid class. Alminoprofen possesses a dual anti-inflammatory action, by inhibiting both secretory phospholipase A2 (sPLA2) and COX-2 .
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Cat. No.: HY-136177
CAS No.: 95906-11-9
Purity:  99.81%
Tris(2,4-di-tert-butylphenyl)phosphate is an active compound from the leaves of Vitex negundo L. shows anti-inflammatory activity with evidence of inhibition for secretory Phospholipase A2 (sPLA2) through molecular docking .
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Cat. No.: HY-11059
CAS No.: 393569-31-8
Purity:  99.47%
Target:  

Phospholipase

Research Areas:  

Inflammation/Immunology

KH064, a D-tyrosine derivative, is an orally active, potent secretory phospholipase A2 (sPLA2) inhibitor with an IC50 of 29 nM for human nonpancreatic secretory PLA2 isoform IIa (hnpsPLA2-IIa). KH064 has anti-inflammatory activity .
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Cat. No.: HY-N7327
CAS No.: 50276-96-5
Ochnaflavone is an inhibitor of IIA-type secretory phospholipase A2 (sPLA2-IIA) with an IC50 of 3.45 µM. Ochnaflavone exhibits significant anti-inflammatory and liver-protective effects, capable of inhibiting the degradation of phosphatidylethanolamine (PE) and lipid peroxidation induced by carbon tetrachloride (CCl4) in rat liver, with an IC50 of 7.16 µM for lipid peroxidation. Ochnaflavone can be used in research on liver damage and inflammatory diseases .
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Cat. No.: HY-120078
CAS No.: 1845753-81-2
Target:  

Phospholipase

Research Areas:  

Cardiovascular Disease

AZD2716 is an orally active secretory phospholipase A2 (sPLA2) inhibitor. AZD2716 inhibits human GIIA sPLA2 (IC50=10 nM), human GV sPLA2 (IC50=40 nM), human GX sPLA2 (IC50=400 nM), snake venom sPLA2 (IC50=2 pM), and snake (Bothrops jararacussu) Lys49-PLA2-like toxin (Kd=110 μM). AZD2716 inhibits sPLA2 isoforms IIa, V, X, snake venom sPLA2s, and snake venom Lys49-PLA2-like toxin myotoxic activity via hydrophobic channel binding. AZD2716 suppresses GIIA sPLA2 production, neutralizes snake venom-induced myotoxicity, and improves survival in envenomed mice. AZD2716 can be used for the research of coronary artery disease, atherosclerosis, and snakebite envenoming [2] .
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Cat. No.: HY-107393
CAS No.: 164083-84-5
Purity:  ≥99.0%
Target:  

Phospholipase

Research Areas:  

Inflammation/Immunology

LY-311727 is a potent secretory non-pancreatic phospholipase A2 (sPLA2) inhibitor (IC50 <1 μM for group IIA sPLA2). sPLA2 is an important proinflammatory enzyme [2].
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Cat. No.: HY-120441
CAS No.: 1101136-50-8
Purity:  ≥98.0%
Synonyms: GK115
CAY10590 (GK115) is an inhibitor of secreted phospholipase A2 (sPLA2) and can be used for the research of chronic inflammatory kidney diseases .
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Cat. No.: HY-P10053
CAS No.: 236394-37-9
Target:  

Phospholipase

Research Areas:  

Metabolic Disease

sPLA2-IIA Inhibitor is a cyclic pentapeptide analog of FLSYK (cyclic 2-Nal-Leu-Ser-2-Nal-Arg (c2)), that binds to hGIIA (human IIA phospholipase A2) and inhibits its hydrolytic ability. sPLA2 is a member of the esterase superfamily that catalyzes the hydrolysis of the ester bond at the sn-2 position of glycerophospholipids, releasing free fatty acids such as arachidonic acid and lysophospholipids .
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Cat. No.: HY-125157
CAS No.: 172732-62-6
Target:  

Phospholipase

Research Areas:  

Inflammation/Immunology

Me-Indoxam is a potent and cell-impermeable secreted phospholipase A2 (sPLA2) inhibitor .
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Cat. No.: HY-W127380
CAS No.: 146797-82-2
Arachidonoyl Thio-PC is a substrate of many phospholipase A2 (PLA2), including sPLA2, cPLA2 and iPLA2. Cleavage of sn-2 fatty acids by PLA2 results in the production of free thiols, which react with chromogenic reagents such as DTNB (Ellman's reagent) and DTP, allowing quantification of PLA2 activity. Isozyme-specific cPLA2 activity can be measured by depleting or inhibiting sPLA2 and iPLA2 activity in the assay.
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Cat. No.: HY-168765
CAS No.: 220862-64-6
Synonyms: LSN433771
Target:  

Phospholipase

Research Areas:  

Cardiovascular Disease

LY433771 (LSN433771) (Compound 8) is a type X secretory phospholipase A2 (sPLA2) inhibitor with an IC50 value of 3 nM, which can be used in the study of cardiovascular diseases [2].
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Cat. No.: HY-169254
Target:  

Phospholipase

Research Areas:  

Metabolic Disease

sPLA2 inhibitor 2 (compound 6a) is a sPLA2 inhibitor, with IC50 of 0.0475 μM. sPLA2 inhibitor 2 can be used in diabetes research .
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Cat. No.: HY-169255
Research Areas:  

Metabolic Disease

sPLA2 inhibitor 3 (Compound 6c) is a potent α-glucosidase inhibitor (IC50 = 0.0953 µM). sPLA2 inhibitor 3 can be used for the research of diabetes .
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Cat. No.: HY-145384
CAS No.: 1048660-43-0
Purity:  99.48%
Target:  

Phospholipase

Research Areas:  

Inflammation/Immunology

ROC-0929 (compound 13a) is a potent and selective inhibitor of secreted phospholipases A2 (sPLA2s) with an IC50 of 80 nM, specially targeting hGX. ROC-0929 inhibits the phosphorylation of ERK1/2 and p-38. Secreted phospholipases A2 (sPLA2s) are a family of disulfide-rich, Ca 2+-dependent enzymes that hydrolyze the sn-2 position of glycero-phospholipids to release a fatty acid and a lysophospholipid. ROC-0929 has the potential for researching inflammation related diseases .
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Cat. No.: HY-112605
CAS No.: 2241025-50-1
Target:  

Phospholipase

Research Areas:  

Cardiovascular Disease

sPLA2-X Inhibitor 31 is a selective secreted phospholipase A2 type X (sPLA2-X) inhibitor with IC50s of 26 nM, 310 nM, and 2230 nM for sPLA2-X, sPLA2-IIa, and sPLA2-V, respectively .
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Cat. No.: HY-136177R
CAS No.: 95906-11-9
Tris(2,4-di-tert-butylphenyl)phosphate (Standard) is the analytical standard of Tris(2,4-di-tert-butylphenyl)phosphate. This product is intended for research and analytical applications. Tris(2,4-di-tert-butylphenyl)phosphate is an active compound from the leaves of Vitex negundo L. shows anti-inflammatory activity with evidence of inhibition for secretory Phospholipase A2 (sPLA2) through molecular docking .
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