314 Results for "

Lipoxygenases

" in MedChemExpress (MCE) Product Catalog:
Products (314)

314 Results for "Lipoxygenases" in MCE Product Catalog:

735
735 Publications Verification
Cat. No.: HY-B0215
CAS No.: 616-91-1
Synonyms: N-Acetylcysteine; N-Acetyl-L-cysteine; NAC
Acetylcysteine (N-Acetylcysteine) is a mucolytic agent that can cross the blood-brain barrier, which reduces the thickness of the mucus. Acetylcysteine is a ROS inhibitor. Acetylcysteine is a cysteine precursor, prevents hemin-induced ferroptosis by neutralizing toxic lipids generated by arachidonate-dependent activity of 5-lipoxygenases. Acetylcysteine induces cell apoptosis. Acetylcysteine also has anti-influenza virus activities. In addition, Acetylcysteine ​​is the most stable form of cysteine ​​during drug delivery and can be used in disulfidptosis studies .
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110
110 Cited Publications
Cat. No.: HY-13419
CAS No.: 112648-68-7
Purity:  98.41%
U-73122 is a phospholipase C (PLC) and 5-LO (5-lipoxygenase) inhibitor with an IC50of 1-2.1 µM for PLC.
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25
25 Cited Publications
Cat. No.: HY-N0551
CAS No.: 524-12-9
Wedelolactone suppresses LPS-induced caspase-11 expression by directly inhibits the IKK Complex. Wedelolactone also inhibits 5-lipoxygenase (5-Lox) with an IC50 of 2.5 μM. Wedelolactone induces caspase-dependent apoptosis in prostate cancer cells via downregulation of PKCε without inhibiting Akt. Wedelolactone can extract from Eclipta alba, and it can be used for the research of cancer .
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24
24 Cited Publications
Cat. No.: HY-14164
CAS No.: 111406-87-2
Purity:  99.61%
Synonyms: A 64077; Abbott 64077
Research Areas:  

Inflammation/Immunology Cancer

Zileuton is a potent and selective inhibitor of 5-lipoxygenase with antiasthmatic properties.
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24
24 Cited Publications
Cat. No.: HY-14164A
CAS No.: 118569-21-4
Purity:  98.61%
Synonyms: A 64077 sodium; Abbott 64077 sodium
Target:  

Lipoxygenase

Research Areas:  

Inflammation/Immunology Cancer

Zileuton sodium (A 64077 sodium) is a potent and selective inhibitor of 5-lipoxygenase, exhibiting inflammatory activities.
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8
8 Cited Publications
Cat. No.: HY-N0198
CAS No.: 500-38-9
Synonyms: NDGA
Nordihydroguaiaretic acid is a 5-lipoxygenase (5LOX) (IC50=8 μM) and tyrosine kinase inhibitor.
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8
8 Cited Publications
Cat. No.: HY-108630
CAS No.: 142878-12-4
Purity:  99.31%
Target:  

Phospholipase

Research Areas:  

Others

U-73343, works as a protonophore, is an inactive analog of U-73122 and can be used as a negative control. U-73343 dose-dependently inhibits acid secretion irrespective of the stimulant. U-73122 is a phospholipase C (PLC) and 5-LO (5-lipoxygenase) inhibitor with an IC50 of 1-2.1 μM for PLC .
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7
7 Cited Publications
Cat. No.: HY-108749
CAS No.: 8001-25-0
Synonyms: Cropure OL
Olive oil (Cropure OL) is an oleaginous compound found in the fruit of the Olea europaea tree . Olive oil contains many phenolic components and exerts antioxidant activity. Olive oil exhibits hydroxyl radical scavenging, platelet aggregation inhibition and xanthine oxidase inhibitory activity. Olive oil can promote wound healing and relieve inflammation. Olive oil can be used for the research of inflammation, cancer, metabolic and cardiovascular disease, such as diabetic foot ulcers and inflammatory bowel disease .
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6
6 Cited Publications
Cat. No.: HY-103157
CAS No.: 4079-26-9
Purity:  99.59%
Synonyms: NSC168807
Target:  

Autophagy Ferroptosis

Research Areas:  

Cardiovascular Disease

PD146176 (NSC168807), a 15-Lipoxygenase (15-LO) inhibitor, inhibits rabbit reticulocyte 15-LO (Ki=197 nM, IC50=0.54 μM). PD146176 reverses cognitive impairment, brain amyloidosis, and tau pathology by stimulating autophagy in aged triple transgenic mice .
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4
4 Cited Publications
Cat. No.: HY-19807
CAS No.: 160807-49-8
Synonyms: Indirubin-3'-oxime
Target:  

GSK-3 CDK Lipoxygenase

Research Areas:  

Cancer

Indirubin-3'-monoxime is a potent GSK-3β inhibitor, and weakly inhibits 5-Lipoxygenase, with IC50s of 22 nM and 7.8-10 µM, respectively; Indirubin-3'-monoxime also shows inhibitory activities against CDK5/p25 and CDK1/cyclin B, with IC50s of 100 and 180 nM.
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3
3 Cited Publications
Cat. No.: HY-12511
CAS No.: 72873-74-6
Purity:  99.91%
Target:  

p38 MAPK

Research Areas:  

Inflammation/Immunology

SKF-86002 is an orally active p38 MAPK inhibitor, with anti-inflammatory, anti-arthritic and analgesic activities. SKF-86002 inhibits lipopolysaccharide (LPS)-stimulate human monocyte IL-1 and TNF-α production (IC50 = 1 μM). SKF-86002 inhibits lipoxygenase- and cyclooxygenase-mediated metabolism of arachidonic acid .
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3
3 Cited Publications
Cat. No.: HY-N6871
CAS No.: 514-10-3
Abietic acid, an orally active diterpene isolated from Colophony, displays significant anti-proliferative, anti-inflammatory, anti-obesity effect, bacteriostatic, cell cycle arresting and pro-apoptotic activities. Abietic acid inhibits lipoxygenase activity for allergy. Abietic acid enhances cell migration and tube formation in HUVECs. Abietic acid induces significant angiogenic potential, which is associated with upregulation of extracellular signal-regulated kinase (ERK) and p38 expression. Abietic acid attenuates sepsis-induced lung injury by inhibiting nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) pathway to inhibit M1 macrophage polarization. Abietic acid exhibits a positive effect against liver injury by attenuating inflammation and ferroptosis. Abietic acid shows accelerated wound closure in a mouse model of cutaneous wounds. Abietic acid significantly reduces the proliferation and growth of NSCLC cells by IKKβ inhibition.Additionally, Abietic acid ameliorates psoriasis-like inflammation and modulates gut microbiota in mice. Abietic acid is promising for research in non-small-cell lung cancer (NSCLC), liver injury-related deseases and psoriasis .
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3
3 Cited Publications
Cat. No.: HY-N1881
CAS No.: 6665-67-4
4',5-Dihydroxyflavone (Compound 2c; Compound B3) is a type of flavonoid compound. 4',5-Dihydroxyflavone can inhibit various oxidases and its IC50 values for collagenase A (ColA) and α-glucosidase are less than 1 μM and 66 μM respectively; for soybean lipoxygenase-1 (LOX-1), its Ki value is 102.6 μM. 4',5-Dihydroxyflavone can be used in studies on anti-toxicity and anti-diabetes .
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3
3 Cited Publications
Cat. No.: HY-N2513
CAS No.: 631-69-6
β-Boswellic acid is isolated from the gum resin of Boswellia serrata with anticancer, antioxidant activity, anti-inflammatory activity and anti-arthritic pain.β-Boswellic acid is an orally active nonreducing-type inhibitor of the 5-lipoxygenase (5-LO) product formation either interacting directly with the 5-LO or blocking its translocation. β-Boswellic acid inhibits the synthesis of DNA, RNA and protein in human leukemia HL-60 cells with IC50 values ranging from 0.6 to 7.1 μM. β-Boswellic acid is promising for research of diabetes, inflammatory and arthritic diseases .
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2
2 Cited Publications
Cat. No.: HY-110399
CAS No.: 34334-69-5
Purity:  99.26%
Cirsiliol is a potent and selective 5-lipoxygenase inhibitor and a competitive low affinity benzodiazepine receptor ligand.
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2
2 Cited Publications
Cat. No.: HY-50714
CAS No.: 147030-01-1
Synonyms: MK-591 sodium
Target:  

FLAP Apoptosis

Research Areas:  

Inflammation/Immunology

Quiflapon sodium (MK-591 sodium) is a selective and specific 5-Lipoxygenase-activating protein (FLAP) inhibitor. Quiflapon sodium is an orally active Leukotriene biosynthesis inhibitor. Induces apoptosis.
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2
2 Cited Publications
Cat. No.: HY-15874
CAS No.: 936350-00-4
Purity:  99.50%
Synonyms: GSK2190915; AM-803
Research Areas:  

Inflammation/Immunology

Fiboflapon (GSK2190915; AM-803) is a potent and orally bioavailable 5-lipoxygenase-activating protein (FLAP) inhibitor with a potency of 2.9 nM in FLAP binding, an IC50 of 76 nM for inhibition of LTB4 in human blood .
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2
2 Cited Publications
Cat. No.: HY-15874A
CAS No.: 1196070-26-4
Purity:  99.46%
Synonyms: GSK2190915 sodium salt; AM-803 sodium
Research Areas:  

Inflammation/Immunology

Fiboflapon sodium (GSK2190915; AM-803) is a potent and orally bioavailable 5-lipoxygenase-activating protein (FLAP) inhibitor with a potency of 2.9 nM in FLAP binding, an IC50 of 76 nM for inhibition of LTB4 in human blood .
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2
2 Cited Publications
Cat. No.: HY-10037
CAS No.: 136668-42-3
Purity:  99.84%
Synonyms: MK-591
Target:  

FLAP Apoptosis

Research Areas:  

Inflammation/Immunology

Quiflapon (MK-591) is a selective and specific 5-lipoxygenase-activating protein (FLAP) inhibitor with an IC50 of 1.6 nM in a FLAP binding assay. Quiflapon is also a potent and orally active Leukotriene biosynthesis (LT) inhibitor, shows IC50 values of 3.1 and 6.1 nM in intact human and elicited rat PMNLs, respectively. Quiflapon induces cell apoptosis .
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