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ML264 - 10mM in DMSO , CAS No.1550008-55-3

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SKU
M421845
Articles du produit groupé
Nom du produit Qté
[M421845-1ml] ML264
Prix Spécial 143,09 € Prix normal 209,91 €

KLF Inhibitors

Information

ML264 ML264 (CID-51003603), a selectively inhibitor of kruppel-like factor 5 (KLF5) ,potently Inhibits Growth of Colorectal Cancer.

Targets

KLF5 (Cell-based assay for proliferation of DLD-1 cells) 29 nM

In vitro

ML264 potently halts DLD-1 viability (IC50 = 29 nM) with high maximal effect (>90%). DLD-1 cells are human colorectal adenocarcinoma cells. ML264 has significant effects at submicromolar doses on other cell types as well, including HCT116 (human colorectal carcinoma), HT29 (human colorectal adenocarcinoma), and SW620 (human colorectal adenocarcinoma). The IEC-6 anti-target (a nontransformed rat intestinal epithelial cell line) is largely unaffected, with inhibition below 50% at the highest dose.This compound potently inhibits proliferation of CRC cells in vitro through modifications of the cell cycle profile.

In vivo

In an established xenograft mouse model of colon cancer, ML264 efficiently inhibits growth of the tumor within five days of treatment. this effect is caused by a significant reduction in proliferation and that ML264 potently inhibits the expression of KLF5 and EGR1, a transcriptional activator of KLF5.

Cell Research(from reference)

Cell lines:DLD-1 and HCT116 colorectal cancer cell lines 

Concentrations:10μM 

Incubation Time:24, 48, 72h 

Plus d’information

Plus d’information
CAS1550008-55-3
Concentration10mM in DMSO
SynonymesCID-510036032-​Propenamide,3-​(3-​chlorophenyl)​-​N-​[2-​[methyl(tetrahydro-​1,​1-​dioxido-​2H-​thiopyran-​4-​yl)​amino]​-​2-​oxoethyl]​-​,(2E)​-
Spécifications et pureté10mM in DMSO
Conditions de stockage de stockageStore at -80°C
Expédié enDry ice packs + Cold packs
Product Description

Information

ML264 ML264 (CID-51003603), a selectively inhibitor of kruppel-like factor 5 (KLF5) ,potently Inhibits Growth of Colorectal Cancer.

Targets

KLF5 (Cell-based assay for proliferation of DLD-1 cells) 29 nM

In vitro

ML264 potently halts DLD-1 viability (IC50 = 29 nM) with high maximal effect (>90%). DLD-1 cells are human colorectal adenocarcinoma cells. ML264 has significant effects at submicromolar doses on other cell types as well, including HCT116 (human colorectal carcinoma), HT29 (human colorectal adenocarcinoma), and SW620 (human colorectal adenocarcinoma). The IEC-6 anti-target (a nontransformed rat intestinal epithelial cell line) is largely unaffected, with inhibition below 50% at the highest dose.This compound potently inhibits proliferation of CRC cells in vitro through modifications of the cell cycle profile.

In vivo

In an established xenograft mouse model of colon cancer, ML264 efficiently inhibits growth of the tumor within five days of treatment. this effect is caused by a significant reduction in proliferation and that ML264 potently inhibits the expression of KLF5 and EGR1, a transcriptional activator of KLF5.

Cell Research(from reference)

Cell lines:DLD-1 and HCT116 colorectal cancer cell lines 

Concentrations:10μM 

Incubation Time:24, 48, 72h 

Pubchem Sid528765520
CibleKLF5
PubChem CID51003603
Formule moléculaireC17H21ClN2O4S

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