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| Product | Description | |
|---|---|---|
| Lipoxin A4 | ethanol solution. Group: Fluorescence/luminescence spectroscopy. |  |
| Lipoxin A4 | Lipoxin A4 (LXA4), an endogenous lipoxygenase-derived eicosanoid mediator, has potent dual pro-resolving and anti-inflammatory properties [1]. Lipoxin A4 inhibits proliferation and inflammatory cytokine/chemokine production of human epidermal keratinocytes (NHEKs) associated with the ERK1/2 and NF-kB pathways [2]. Lipoxin A4 inhibits serum amyloid A (SAA)-mediated IL-8 release with an IC 50 value of 25.74 nM [3]. Uses: Scientific research. Group: Natural products. Alternative Names: LXA4. CAS No. 89663-86-5. Pack Sizes: 25 μg (283.71 μM * 250 μL in Ethanol). Product ID: HY-113509. |  |
| Lipoxin A4 (15-epi-lipoxin A4, 5,6,15-trihydroxy-7,9,11,13-eicosatetraenoic acid, LXA4, 5(S),6(R)-Lipoxin A4) | Lipoxin A4 (15-epi-lipoxin A4, 5,6,15-trihydroxy-7,9,11,13-eicosatetraenoic acid, LXA4, 5(S),6(R)-Lipoxin A4). Group: Biochemicals. Alternative Names: (5S, 6R, 7E, 9E, 11Z, 13E, 15S)-5, 6, 15-trihydroxyicosa-7, 9, 11, 13-tetraenoic acid. Grades: Highly Purified. CAS No. 89663-86-5. Pack Sizes: 25ug, 100ug. Molecular Formula: C20 H32 O5, Molecular Weight: 352.5. US Biological Life Sciences. |  Worldwide |
| BML 111 | BML 111 is a FPR2 (lipoxin A4 receptor) agonist. It inhibits tumor-related angiogenesis and reduces tumor growth in hepatoma H22 cell bearing mice. BML 111 also protects against hemorrhagic shock-induced acute lung injury in rats and attenuates renal ischemia/reperfusion injury. Synonyms: BML-111; BML 111; BML111. (5S,6R)-Methyl 5,6,7-trihydroxyheptanoate; methyl (5S,6R)-5,6,7-trihydroxyheptanoate. CAS No. 78606-80-1. Molecular formula: C8H16O5. Mole weight: 192.21. |  |
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