LR-90
CAS No. 245075-84-7
LR-90( —— )
Catalog No. M26283 CAS No. 245075-84-7
LR-90 is also used in the research of diabetic animal model.LR-90 is an advanced glycation end product (AGE) inhibitor, inhibits inflammatory responses in human monocytes.?
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 87 | Get Quote |
|
| 5MG | 147 | Get Quote |
|
| 10MG | 258 | Get Quote |
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| 25MG | 484 | Get Quote |
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| 50MG | 700 | Get Quote |
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| 100MG | 981 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameLR-90
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NoteResearch use only, not for human use.
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Brief DescriptionLR-90 is also used in the research of diabetic animal model.LR-90 is an advanced glycation end product (AGE) inhibitor, inhibits inflammatory responses in human monocytes.?
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DescriptionLR-90 is also used in the research of diabetic animal model.LR-90 is an advanced glycation end product (AGE) inhibitor, inhibits inflammatory responses in human monocytes.?(In Vitro):LR-90 (0, 25, 50, 100, and 200 μM) dose-dependently and significantly blocks THP-1 cells adherence to endothelial cells after pretreatment 1 h befor S100b stimulatation for 24 hours.?LR-90 (0, 25, 50, 100, and 200 μM, for 24 hours) shows no effect on the cell viability of THP-1 cells.LR-90 (0, 25, 50, 100, and 200 μM) inhibits RAGE, MCP-1, COX-2, IP-10 and NOX2 mRNA expression in THP-1 cells in a dose-dependent manner, after pretreatment 1 h befor S100b stimulatation for 4 hours.(In Vivo):LR-90 (50 mg/L) decreases renal AGE, AGER and lipid peroxidation.LR-90 (50 mg/L, p.o. for 27 weeks) significantly reduces plasma lipids, modestly affects hyperglycaemia in ZDF rats.
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In VitroLR-90 (0, 25, 50, 100, and 200 μM) inhibits RAGE, MCP-1, COX-2, IP-10 and NOX2 mRNA expression in THP-1 cells in a dose-dependent manner, after pretreatment 1 h befor S100b stimulatation for 4 hours.LR-90 (0, 25, 50, 100, and 200 μM) dose-dependently and significantly blocks THP-1 cells adherence to endothelial cells after pretreatment 1 h befor S100b stimulatation for 24 hours.LR-90 (0, 25, 50, 100, and 200 μM, for 24 hours) shows no effect on the cell viability of THP-1 cells. Cell Viability Assay Cell Line:THP-1 cells Concentration:0, 25, 50, 100, and 200 μM Incubation Time:24 hours Result:Showed no cytotoxicity to THP-1 cells.RT-PCR Cell Line:THP-1 cells Concentration:0, 25, 50, 100, and 200 μM Incubation Time:One hour before S100b addition for 4 hours Result:Dose-dependently inhibited mRNA expression of RAGE, MCP-1, COX-2, IP-10, and NOX2 stimulated with S100b.
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In VivoLR-90 (50 mg/L, p.o. for 27 weeks) significantly reduces plasma lipids, modestly affects hyperglycaemia in ZDF rats.LR-90 (50 mg/L) decreases renal AGE, AGER and lipid peroxidation. Animal Model:Male ZDF rats (13 to 40 weeks)Dosage:50 mg/L Administration:P.O. for 27 weeks Result:Significantly reduced plasma triacylglycerol and cholesterol by ~55% and ~30%, respectively. Modestly affected hyperglycaemia and blood pressure. Lowered the body weight.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorBRD4
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Research Area——
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Indication——
Chemical Information
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CAS Number245075-84-7
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Formula Weight709.58
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Molecular FormulaC35H34Cl2N4O8
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : ≥ 100 mg/mL (140.93 mM)
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SMILESCC(C)(Oc1ccc(NC(=O)Nc2ccc(Cc3ccc(NC(=O)Nc4ccc(OC(C)(C)C(O)=O)cc4)c(Cl)c3)cc2Cl)cc1)C(O)=O
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Chemical Name——
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.Susanta Samajdar, et al. Bicyclic heterocyclic derivatives as bromodomain inhibitors. WO2015104653A1
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