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1、Hotline: 400-820-3792Inhibitors Agonists Screening Librarieswww.MedChemENiclosamideCat. No.: HY-B0497CAS No.: 50-65-7Synonyms: BAY2353分式: CHClNO分量: 327.12作靶点: STAT作通路: JAK/STAT Signaling; Stem Cell/Wnt储存式: Powder -20C 3 years4C 2 yearsIn solvent -80C 6 months-20C 1 month溶解性数据体外实验 DMF : 9.42 mg/mL (2
2、8.80 mM; Need ultrasonic and warming)Mass Solvent1 mg 5 mg 10 mg Concentration制备储备液1 mM 3.0570 mL 15.2849 mL 30.5698 mL5 mM 0.6114 mL 3.0570 mL 6.1140 mL10 mM 0.3057 mL 1.5285 mL 3.0570 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 Niclosamide (BAY2353)种服物可利的氯化杨酰苯胺,具有驱和潜在的抗肿瘤活
3、性。Niclosamide (BAY2353) 可抑制STAT3,在 HeLa 细胞中IC50 0.25 M,并在细胞试验中抑制 DNA 复制。IC50 & Target STAT30.25 M (IC50, in HeLa cells)1/3 Master of Small Molecules 您边的抑制剂师www.MedChemE体外研究 Niclosamide is an inhibitor of STAT3, inhibiting STAT3-mediated luciferase reporter activity with an IC50 of0.25 M in HeLa cell
4、s. Niclosamide (1 M) inhibits the EGF-induced nuclear translocation of STAT3 in Du145cells. Niclosamide ( 1. Niclosamide can block SARS-CoV replication at a micromolar concentration in VeroE6 cells infected with SARS-CoV 2. Niclosamide ( 3. Niclosamide inhibits the TNF-induced NF-B reporteractivity
5、in a dose- and time-dependent manner in U2OS cells. Niclosamide (125 nM) inhibits NF-B activationinduced by p65, IKK, IKK, IKK, and TAK1 in U2OS cells. Niclosamide ( 4.体内研究 Niclosamide (40 mg/kg/d, i.p.) suppresses the growth of xenografted AML cells in nude mice bearing HL-60 xenograft tumors 4.PRO
6、TOCOLKinase Assay 1 All of the protein kinases are expressed either in Sf9 insect cells or in E.coli as recombinant GST-fusionproteins or His-tagged proteins. A radiometric protein kinase assay is used for measuring the kinase activityof the 22 protein kinases. Briefly, for each protein kinase, 50 L
7、 reaction cocktail containing 60 mM HEPES-NaOH, 3 mM MgCl2, 3 mM MnCl2, 3 M Na-orthovanadate, 1.2 mM DTT, 50 g/mL PEG20000, 1 M -33P-ATP, Niclosamide, adequate amount of enzyme and its substrate. The PKC-alpha assay additionallycontain 1 mM Ca2, 4 mM EDTA, 5 g/mL phosphatidylserine and 1 g/mL 1, 2-D
8、ioleyl-glycerol. The reactioncocktails are incubated at 37C for 60 minutes and stop with 50 L 2% (v/v) H3PO4. Incorporation of 33Pi isdetermined with a microplate scintillation counter. The activities and the IC50 values are calculated usingQuattro Workflow V2.28.MCE has not independently confirmed
9、the accuracy of these methods. They are for reference only.Cell Assay 1 Cells are plated in 96-well culture plates with cell density of 3-4 103 cells/well and treat with Niclosamide byadding 100 L medium containing Niclosamide of various concentrations on the second day. After 72-hourstreatment, MTT
10、 is added to each well and incubated for additional 4-5 hours, and the absorbance ismeasured on a microplate reader at 570 nm. Cell growth inhibition is evaluated as the ratio of theabsorbance of the sample to that of the control. The results are representative of at least 3 independentexperiments.M
11、CE has not independently confirmed the accuracy of these methods. They are for reference only.Animal Male nu/nu BALB/c mice are used in the assay. HL-60 cells are inoculated s.c. on the flanks of 4- to 6-wk-oldAdministration 4 mice. Tumors are measured every other day with use of calipers. Mice bear
12、ing HL-60 xenografts arerandomized to receive treatment with normal saline (control) or p-niclosamide for 15 days (n=7 animalseach). Tumor volumes are calculated by the following formula: a2b0.4, where a is the smallest diameterand b is the diameter perpendicular to a. After mice are euthanized, xen
13、ografts are dissected, weighed, orpreserved.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 Cell Syst. 2018 Apr 25;6(4):424-443.e7. Patent. US20180263995A1.2/3 Master of Small Molecules 您边的抑制剂师www.MedChemESee more customer validations on HYP
14、ERLINK / www.MedChemEREFERENCES1. Ren, X., et al., Identification of niclosamide as a new small-molecule inhibitor of the STAT3 signaling pathway. ACS Medicinal ChemistryLetters, 2010. 1(9): p. 454-459.2. Wu CJ, et al. Inhibition of severe acute respiratory syndrome coronavirus replication by niclos
15、amide. Antimicrob Agents Chemother.2004 Jul;48(7):2693-6.3. Chen, M., et al., The anti-helminthic niclosamide inhibits Wnt/Frizzled1 signaling. Biochemistry, 2009. 48(43): p. 10267-74.4. Jin, Y., et al. Antineoplastic mechanisms of niclosamide in acute myelogenous leukemia stem cells: inactivation of the NF-kappaBpathway and generation of reactive oxygen species. Cancer R
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