[CAS NO. 50-65-7]  Niclosamide (BAY2353)

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PRODUCTS SPECIFICATIONS [50-65-7]

Store
Catalog
SLK-S3030
Brand
Selleck
CAS
50-65-7

DESCRIPTION [50-65-7]

Overview

MDL-
Molecular Weight327.12
Molecular FormulaC13H8Cl2N2O4
SMILESC(NC1=C(Cl)C=C(N(=O)=O)C=C1)(=O)C2=C(O)C=CC(Cl)=C2

For research use only.

Storage

3 years,-20°C,powder
1 years,-80°C,in solvent

Shipping

Room temperature shipping(Stability testing shows this product can be shipped without any cooling measures.)

Preparing Stock Solutions

1 mg5 mg10 mg
1 mM3.0570 mL15.2849 mL30.5698 mL
5 mM0.6114 mL3.0570 mL6.1140 mL
10 mM---
50 mM---

Description

Niclosamide (BAY2353, Niclocide, NSC 178296) can inhibit and inhibit with of 0.7 μM in a cell-free assay. Niclosamide selectively inhibited the phosphorylation of STAT3 and had no obvious inhibition against the activation of other homologues (e.g., STAT1 and STAT5).

Targets

STAT3 [1]
(in Hela cells)
0.7 μM

In vitro

Niclosamide (< 5 μM) dose dependently inhibits STAT3-mediated luciferase reporter activity with IC50 of 0.25 μM in HeLa cells. Niclosamide(< 2 μM) dose dependently inhibits the phosphorylation of STAT3 in Du145 cells. Niclosamide (1 μM) inhibits the EGF-induced nuclear translocation of STAT3 in Du145 cells. Niclosamide(< 2 μM) dose dependently inhibits the transcription of STAT3 downstream genes in Du145 cells. Niclosamide(< 10 μM) dose dependently induces G0/G1 arrest and apoptosis of Du145 cancer cells. Niclosamide is able to inhibit SARS-CoV replication at a micromolar concentration in Vero E6 cells infected with SARS-CoV. Niclosamide(< 7.5 μM) promotes Frizzled1 endocytosis, downregulates Dishevelled-2 protein, and inhibits Wnt3A-stimulated beta-catenin stabilization and LEF/TCF reporter activity in U2OS cells. Niclosamide inhibits the TNF-induced NF-κB reporter activity in a dose- and time-dependent manner in U2OS cells. Niclosamide(125 nM) inhibits NF-κB activation induced by p65, IKKα, IKKβ, IKKγ, and TAK1 in U2OS cells. Niclosamide(< 500 nM) completely block the time- and dose-dependent TNFα-induced alteration of the NF-κB–DNA complex in HL-60 cells. Niclosamide(< 10 nM) inhibits constitutive NF-κB activation in U266 cells. Niclosamide inhibits TNF-induced degradation of IκBα and relocation of p65 in a dose- and time-dependent manner in HL-60, Molm13, or AML primary cells. Niclosamide(500 nM) decreases TNF-induced NF-κB–dependent gene products involved in cell survival in HL-60 cells. Niclosamide dose dependently inhibits the growth and induces robust apoptosis of AML cells associated with decreased Mcl-1 and XIAP levels and increased intracellular ROS levels.

In vivo

Niclosamide(40 mg/kg/d, i.p.) inhibits growth of xenografted AML cells in nude mice bearing HL-60 xenograft tumors.


Synonyms

Benzamide, 5-chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxy-
Salicylanilide, 2′,5-dichloro-4′-nitro-
5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide
Bayluscid
5-Chloro-2′-chloro-4′-nitrosalicylanilide
N-(2-Chloro-4-nitrophenyl)-5-chlorosalicylamide
2′,5-Dichloro-4′-nitrosalicylanilide
HL 2447
2-Hydroxy-5-chloro-N-(2-chloro-4-nitrophenyl)benzamide
Iomesan
Niclosamide
Phenasal
Vermitin
Yomesan
2-Chloro-4-nitrophenylamide-6-chlorosalicylic acid
Fenasal
N-(2′-Chloro-4′-nitrophenyl)-5-chlorosalicylamide
Mansonil
Radeverm
5-Chloro-N-(2′-chloro-4′-nitrophenyl)salicylamide
Bayer 2353
Lintex
Nasemo
Sulqui
Tredemine
Sagimid
Devermin
Devermine
Cestocid
Mato
Vermitid
Helmiantin
Fedal-Telmin
BAY 2353
Zestocarp
WR 46234
Utosamide
Niclocide
Cestocide
Ruby
NSC 178296