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Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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SKU | Size | Availability | Price | Qty |
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M413940-5mg | 5mg | 3 | $98.90 | |
M413940-10mg | 10mg | 3 | $137.90 | |
M413940-25mg | 25mg | 2 | $310.90 | |
M413940-50mg | 50mg | 2 | $434.90 | |
M413940-100mg | 100mg | 2 | $652.90 |
KLF Inhibitors
Specifications & Purity | ≥98% |
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Biochemical and Physiological Mechanisms | ML264 (CID-51003603), a selectively inhibitor of kruppel-like factor 5 (KLF5),potently Inhibits Growth of Colorectal Cancer. |
Storage Temp | Store at -20°C |
Shipped In | Ice chest + Ice pads |
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 |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Pubchem Sid | 504771001 |
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Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504771001 |
IUPAC Name | (E)-3-(3-chlorophenyl)-N-[2-[(1,1-dioxothian-4-yl)-methylamino]-2-oxoethyl]prop-2-enamide |
INCHI | InChI=1S/C17H21ClN2O4S/c1-20(15-7-9-25(23,24)10-8-15)17(22)12-19-16(21)6-5-13-3-2-4-14(18)11-13/h2-6,11,15H,7-10,12H2,1H3,(H,19,21)/b6-5+ |
InChi Key | AJCDZIDKYKCOMZ-AATRIKPKSA-N |
Canonical SMILES | CN(C1CCS(=O)(=O)CC1)C(=O)CNC(=O)C=CC2=CC(=CC=C2)Cl |
Isomeric SMILES | CN(C1CCS(=O)(=O)CC1)C(=O)CNC(=O)/C=C/C2=CC(=CC=C2)Cl |
PubChem CID | 51003603 |
Molecular Weight | 384.88 |
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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Certificate of Analysis | Jun 05, 2023 | M413940 | |
Certificate of Analysis | Jun 05, 2023 | M413940 | |
Certificate of Analysis | Jun 05, 2023 | M413940 | |
Certificate of Analysis | Jun 05, 2023 | M413940 | |
Certificate of Analysis | Jun 05, 2023 | M413940 | |
Certificate of Analysis | Jun 05, 2023 | M413940 | |
Certificate of Analysis | Jun 05, 2023 | M413940 | |
Certificate of Analysis | Jun 05, 2023 | M413940 | |
Certificate of Analysis | Jun 05, 2023 | M413940 | |
Certificate of Analysis | Jun 05, 2023 | M413940 |
Solubility | Solubility (25°C) In vitro DMSO: 76 mg/mL (197.46 mM); Water: Insoluble; Ethanol: Insoluble; |
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Molecular Weight | 384.900 g/mol |
XLogP3 | 1.700 |
Hydrogen Bond Donor Count | 1 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 5 |
Exact Mass | 384.091 Da |
Monoisotopic Mass | 384.091 Da |
Topological Polar Surface Area | 91.900 Ų |
Heavy Atom Count | 25 |
Formal Charge | 0 |
Complexity | 601.000 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 1 |
Undefined Bond Stereocenter Count | 0 |
The total count of all stereochemical bonds | 1 |
Covalently-Bonded Unit Count | 1 |
RIDADR | NONHforallmodesoftransport |
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Starting at $241.90