LMT-28
CAS No. 1239600-18-0
LMT-28( C25H32F3N5O4 )
Catalog No. M10966 CAS No. 1239600-18-0
LMT-28 (LMT28) is a specific blocker of IL-6 signaling via inhibits IL-6Rβ (gp130) with IC50 of 5.9 uM (IL-6–induced luciferase activity).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 58 | In Stock |
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| 10MG | 102 | In Stock |
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| 25MG | 222 | In Stock |
|
| 50MG | 350 | In Stock |
|
| 100MG | 512 | In Stock |
|
| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameLMT-28
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NoteResearch use only, not for human use.
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Brief DescriptionLMT-28 (LMT28) is a specific blocker of IL-6 signaling via inhibits IL-6Rβ (gp130) with IC50 of 5.9 uM (IL-6–induced luciferase activity).
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DescriptionLMT-28 (LMT28) is a specific blocker of IL-6 signaling via inhibits IL-6Rβ (gp130) with IC50 of 5.9 uM (IL-6–induced luciferase activity), selectively inhibits IL-6–induced phosphorylation of STAT3, JAK2, and gp130; does not affect LIF-induced STAT3 activation and not inhibit IL-11 stimulation on HepG2 cells; binds directly and specifically to gp130, and thereby inhibits the interaction of gp130 with the IL-6/IL-6Rα complex; inhibits IL-6–induced proliferation of the human erythroleukemic cell line TF-1 with IC50 of 7.5 uM; inhibits IL-6–induced TNF-α production, ameliorates the progression of pancreatitis in mice.
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In VitroCell Proliferation Assay Cell Line:TF-1 cells (1 ng/mL IL-6-induced)Concentration:1, 10, 100, 1000, 10000 nM Incubation Time:72 hours Result:Markedly inhibited IL-6–induced TF-1 proliferation with an IC50 value of 7.5 μM.Western Blot Analysis Cell Line:HepG2 cells (treated with 10 ng/mL IL-6) Concentration:1, 3, 10, 30, and 100 μM Incubation Time:1 hour Result:Inhibits IL-6-induced phosphorylation of STAT3, JAK2, and gp130.
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In VivoAnimal Model:Six-week-old male DBA/1J mice (collagen-induced arthritis mice, CIA)Dosage:0-0.5 mg/kg Administration:Oral; once daily for 15 days Result:Markedly reduced the serum levels of cartilage oligomeric matrix protein (COMP) by 50%, serum amyloid P (SAP) by 55%, and anti-CII IgG by 62%.
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SynonymsC25H32F3N5O4
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PathwayApoptosis
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TargetIL Receptor
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RecptorInterleukin Receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number1239600-18-0
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Formula Weight311.422
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Molecular FormulaC17H29NO4
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (321.11 mM)
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SMILESO=C1OC[C@H](C(C)C)N1C([C@@H](C)[C@H](O)C(CCCCC)=C)=O
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Chemical Name(S)-3-((2S,3S)-3-hydroxy-2-methyl-4-methylenenonanoyl)-4-isopropyloxazolidin-2-one
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Hong SS, et al. J Immunol. 2015 Jul 1;195(1):237-45.
2. Armstead WM, et al. Transl Stroke Res. 2018 Feb 23. doi: 10.1007/s12975-018-0617-z.
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