28 Results for "

5-lipoxygenase-activating

" in MedChemExpress (MCE) Product Catalog:
Products (28)

28 Results for "5-lipoxygenase-activating" in MCE Product Catalog:

  • Targets Recommended:
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-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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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-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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1
1 Cited Publications
Cat. No.: HY-128171
CAS No.: 724453-98-9
Purity:  99.67%
Target:  

FLAP Epoxide Hydrolase

Research Areas:  

Inflammation/Immunology

Diflapolin is a highly active dual 5-lipoxygenase-activating protein (FLAP)/soluble epoxide hydrolase (sEH) inhibitor with marked anti-inflammatory efficacy and high target selectivity. Diflapolin inhibits 5-LOX product formation in intact human monocytes and neutrophils with IC50s?of? 30 and 170?nM, respectively, and suppressed the activity of isolated sEH (IC50=20?nM) .
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Cat. No.: HY-122908
CAS No.: 2041075-86-7
Purity:  98.97%
Synonyms: AZD5718
Target:  

FLAP

Research Areas:  

Cardiovascular Disease

Atuliflapon (AZD5718) is an orally active inhibitor of FLAP (5?Lipoxygenase activating protein), with an IC50 of 2 nM. Atuliflapon is used in the study for coronary artery disease .
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Cat. No.: HY-14460
CAS No.: 1206880-66-1
Purity:  99.72%
Target:  

FLAP

Research Areas:  

Inflammation/Immunology

AM679 is a potent, selective 5-lipoxygenase-activating protein (FLAP) inhibitor with an IC50 of 2 nM in a human FLAP membrane binding assay. AM679 markedly reduces the respiratory syncytial virus-driven ocular pathology as well as the synthesis of cysteinyl leukotrienes (CysLTs) in the eye .
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Cat. No.: HY-14165
CAS No.: 128253-31-6
Purity:  99.48%
Synonyms: BAY X 1005; DG-031
Veliflapon (BAY X 1005; DG-031) is an orally active and selective 5-lipoxygenase activating protein (FLAP) inhibitor . Veliflapon inhibits the synthesis of the leukotrienes B4 and C4 .
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Cat. No.: HY-12995A
CAS No.: 1360550-05-5
Target:  

FLAP

Research Areas:  

Inflammation/Immunology

(S)-BI 665915 is an orally active oxadiazole-containing 5-lipoxygenase-activating protein (FLAP) inhibitor with an IC50 of 1.7 nM for FLAP binding. (S)-BI 665915 inhibits FLAP functional in human whole blood with an IC50 of 45 nM. (S)-BI 665915 demonstrates an excellent cross-species agent metabolism and pharmacokinetics (DMPK) profile and a dose-dependent inhibition of LTB4 production .
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Cat. No.: HY-12995
CAS No.: 1360550-04-4
Target:  

FLAP

BI 665915, a chemical probe, is an orally active and potent 5-lipoxygenase-activating protein (FLAP) inhibitor. BI 665915 inhibits FLAP production that blocks LTB4 biosynthesis in mice. BI 665915 is promising for research of various inflammatory diseases, including respiratory and cardiovascular diseases .
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Cat. No.: HY-12996
CAS No.: 1643809-54-4
Research Areas:  

Inflammation/Immunology

AZD6642 is a 5-lipoxygenase activating protein (FLAP) inhibitor. AZD6642 can effectively inhibit the production of LTB4. AZD6642 exhibits high oral bioavailability in rats and dogs. AZD6642 can be used in the research of inflammatory diseases .
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Cat. No.: HY-179441
Target:  

Epoxide Hydrolase FLAP

Research Areas:  

Inflammation/Immunology

sEH/FLAP-IN-2 is a selective sEH (IC50 = 12.6 nM)/FLAP dual inhibitor. sEH/FLAP-IN-2 highlights the reduction of 5-LOX/FLAP- and sEH-derived LMs, resulting in a favourable redistribution of LMs. sEH/FLAP-IN-2 can be used for the study of peritonitis .
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Cat. No.: HY-156194
CAS No.: 2041076-43-9
Target:  

FLAP

Research Areas:  

Cardiovascular Disease

FLAP-IN-1 (Intermediate 14) is a 5-lipoxygenase-activating protein (FLAP) inhibitor with an IC50 value of 654 nM. FLAP-IN-1 can be used in cardiovascular disease research .
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Cat. No.: HY-50714R
CAS No.: 147030-01-1
Synonyms: MK-591 sodium (Standard)
Research Areas:  

Inflammation/Immunology

Quiflapon (sodium) (Standard) is the analytical standard of Quiflapon (sodium). This product is intended for research and analytical applications. 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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Cat. No.: HY-118979
CAS No.: 144210-49-1
Target:  

Leukotriene Receptor

Research Areas:  

Inflammation/Immunology

L-691678 can bind to FLAP by recognizing the amino acid residues of 5-lipoxygenase-activating protein (FLAP), thereby inhibiting leukotriene biosynthesis. L-691678 can be used in the study of leukotriene-related diseases such as allergies, asthma, and inflammation .
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Cat. No.: HY-113628
CAS No.: 189498-57-5
Synonyms: VML-530
Target:  

FLAP

Research Areas:  

Inflammation/Immunology

ABT-080 is an orally active inhibitor of leukotriene biosynthesis that targets 5-lipoxygenase-activating protein (FLAP). ABT-080 inhibits leukotriene production in intact human neutrophils, mouse peritoneal macrophages and human whole blood, with IC50 values of 20 nM, 0.16 nM and 13 μM, respectively. ABT-080 blocks the leukotriene pathway leading to the synthesis of LTB4 and LTC4, but does not block PGH2 biosynthesis. ABT-080 inhibits leukotriene biosynthesis and bronchoconstriction in mouse models. ABT-080 is used in research related to asthma, pleurisy and allergy .
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Cat. No.: HY-151619
Target:  

Epoxide Hydrolase

Research Areas:  

Inflammation/Immunology

sEH inhibitor-12 (compound 34) is a sEH inhibitor with an IC50 value of 0.7 μM. sEH inhibitor-12 inhibits the 5-lipoxygenase-activating protein (FLAP)-mediated leukotriene (LT) biosynthesis with an IC50 value of 2.9 μM. sEH inhibitor-12 can be used for the research of inflammation .
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Cat. No.: HY-155204
Research Areas:  

Inflammation/Immunology

LTB4-IN-2 (Comopund 6x) is a Leukotriene B4 (LTB4) inhibitor. LTB4-IN-2 inhibits Leukotriene B4 formation (IC50: 1.15 μM) by selectively targeting 5-Lipoxygenase-activating protein (FLAP). LTB4-IN-2 can be used for anti-inflammatory research .
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Cat. No.: HY-10037R
CAS No.: 136668-42-3
Synonyms: MK-591 (Standard)
Research Areas:  

Inflammation/Immunology

Quiflapon (Standard) is the analytical standard of Quiflapon. This product is intended for research and analytical applications. 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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Cat. No.: HY-P811356
Synonyms: FLAP, ALOX5AP, Arachidonate 5-lipoxygenase-activating protein, MK-886-binding protein

Host:  

Rabbit

Application:  

WB, IHC-P

Reactivity:  

Human

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