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1、Hotline: 400-820-3792Inhibitors Agonists Screening Librarieswww.MedChemEE6446 dihydrochlorideCat. No.: HY-12756ACAS No.: 1345675-25-3Synonyms: E-6446 dihydrochloride分式: CHClNO分量: 522.51作靶点: Toll-like Receptor (TLR)作通路: Immunology/Inflammation储存式: Powder -20C 3 years4C 2 yearsIn solvent -80C 6 months

2、-20C 1 month溶解性数据体外实验 DMSO : 7.6 mg/mL (14.55 mM; Need ultrasonic and warming)Mass Solvent1 mg 5 mg 10 mg Concentration制备储备液1 mM 1.9138 mL 9.5692 mL 19.1384 mL5 mM 0.3828 mL 1.9138 mL 3.8277 mL10 mM 0.1914 mL 0.9569 mL 1.9138 mL请根据产品在不同溶剂中的溶解度,选择合适的溶剂配制储备液,并请注意储备液的保存式和期限。BIOLOGICAL ACTIVITY物活性 E6446

3、 dihydrochloride种有效的、可服的 TLR7 和 TLR9 拮抗剂,可于有害炎症反应的研究。IC50 & Target TLR7, TLR9 1体外研究E6446 dihydrochloride is a potent and orally acitve TLR7 and TLR9 inhibitor. E6446 potently suppressesDNA stimulation of HEK:TLR9 cells, with an IC50 value of 10 nM, but is significantly less effective at1/3 Master of

4、 Small Molecules 您边的抑制剂师www.MedChemEsuppressing LPS endotoxin stimulation of HEK:TLR4 cells or R848 stimulation of HEK:TLR7 cells. E6446potently inhibits IL-6 production induced by CpG2216 but is ineffective against induction by the TLR3 ligandpoly inosine-cytosine. The ability of E6446 to inhibit T

5、LR7 is ligand dependent, E6446 is a potent inhibitor ofIL-6 induction by RNA but a relatively poor inhibitor of IL-6 induction by the small molecule imidazoquinolineligand R-848. E6446 suppress TLR9-DNA interaction in vitro, with an IC50 in the 1 to 10 M range 1. E6446(0.01-0.03 M) specifically inhi

6、bits TLR9 activation with CpG ODN 2006, and blocks TLR7/8 activated by theimidazoquinoline compound R848 at 2-8 M. E6446 reduces 50% of TLR4 activation at 30 M, and showsIC50s of 0.01 M and 0.23 M in HEK-TLR9 cells stimulated with oligo 2006 and in human PBMCsstimulated with oligo 2216, respectively

7、 2.体内研究 E6446 (20 mg/kg, p.o.) almost cmlpletely inhibits CpG1668-induced IL-6 production, and dose-dependentlysuppresses the development of ANA (anti-nuclear antibodies) in mice at 20 and 60 mg/kg 1. E6446 (20, 60mg/kg, p.o.) dose-dependently inhibits TLR9 signaling in mice. E6446 (60, 120 mg/kg, p

8、.o.) preventshyperresponsiveness of TLRs and LPS-induced septic shock in rodent malaria, diminishes TLRresponsiveness during acute malaria, suppresses activation of both TLR7 and TLR9 2.PROTOCOLCell Assay 1 E6446 is assayed for the suppression of BALB/c mouse spleen interleukin-6 (IL-6) production i

9、n response tostimulation by oligonucleotide CpG1668. E6446 is added to dissociated splenocytes (5 105 per well incomplete RPMI/10% fetal bovine serum in a 96-well plate) before addition of TLR agonists. Cells arestimulated for 72 hours, and supernatants are removed for ELISA analysis of IL-6. Mouse

10、bone marrow-derived dendritic cells (BMDCs) are generated by culturing BALB/c marrow cells in RPMI containing 100ng/mL Flt3 ligand for 7 days. Cells (1 105) in 50 L are assayed for IL-6 production after overnight or 24-hour stimulation with various TLR ligands. For studies using human peripheral blo

11、od mononuclear cells,Ficoll-separated mononuclear cells are isolated from healthy volunteer donors, washed, and plated withstimulatory oligonucleotide CpG2216 in complete RPMI for 72 hours. Interferon in supernatant is quantifiedby ELISA 1.MCE has not independently confirmed the accuracy of these me

12、thods. They are for reference only.Animal Mice 1Administration 1 MRL/lpr mice are dosed orally five times a week with 20 or 60 mg/kg E6446 or 60 mg/kg hydroxychloroquinebeginning at 5 weeks of age. Cytoxan is administered at 50 mg/kg i.p. every 10 days. A serum sample istaken immediately before the

13、beginning of treatment to monitor changes in autoreactive antibodies.Subsequently, serum samples are collected approximately monthly and analyzed for anti-dsDNA by ELISAafter 1:500 dilution. Body weights and urine samples are taken at the same interval, and proteinuria isassessed by ChemStrips. Anti

14、-nuclear antibodies (ANA) are assessed using commercially available HEp2slide kits, with serum diluted to 1:100 in kit buffer. ANA scores are read blinded 1.MCE has not independently confirmed the accuracy of these methods. They are for reference only.户使本产品发表的科研献2/3 Master of Small Molecules 您边的抑制剂师

15、www.MedChemE Oxid Med Cell Longev. 2019 Apr. Vet Microbiol. 2017 Aug;207:56-62.See more customer validations on HYPERLINK / www.MedChemEREFERENCES1. Lamphier M, et al. Novel small molecule inhibitors of TLR7 and TLR9: mechanism of action and efficacy in vivo. Mol Pharmacol. 2014Mar;85(3):429-40.2. Franklin BS, et al. Therapeutical targeting of nucleic acid-sensing Toll-like receptors prevents experimental cerebral malaria. Proc NatlAcad Sci U

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