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Postion:Product Catalog >Biochemical Engineering>Inhibitors>DNA damage>DNA / RNA Synthesis inhibitors>CX-5461
CX-5461
  • CX-5461

CX-5461 NEW

Price $39 $80 $133
Package 2mg 5mg 10mg
Supply Ability: 10g
Update Time: 2026-06-15

Product Details

Product Name: CX-5461 CAS No.: 1138549-36-6
Purity: 99.40% Supply Ability: 10g
Release date: 2026/06/15

Product Introduction

Bioactivity

NameCX-5461
DescriptionCX5461 is an rRNA synthesis inhibitor with oral activity that inhibits Pol I-driven rRNA transcription. CX5461 activates the DNA damage response and has antitumor activity in tumors such as ovarian cancer.
Cell ResearchCells are plated on 96-well plates and treated the next day with dose response of CX-5461 for 96 hours. Cell viability is determined using Alamar Blue and CyQUANT assays(Only for Reference)
Kinase AssayPol I and Pol II Transcription Assay: Two short-lived RNA transcripts (half-lives ~20-30 minutes), one produced by Pol I and another by Pol II, are quantitated by qRT-PCR as a measure of CX-5461-related effects on transcription. The 45S pre-rRNA served as the Pol I transcript and the mRNA for the protooncogene c-myc served as the comparator Pol II transcript. Both Pol I and Pol II transcription are known to be affected by general cellular stress. To minimize the potential effects of such stress, cells are exposed to test agents for only a short period of time (2 hours). This is sufficient time for these transcripts to be reduced by greater than 90% if CX-5461 affects their synthesis.
In vitroMETHODS: The phytopathogenic fungi A. tubingensis, Nigrospora oryzae and Phoma herbarum were treated with Carviolin (1-512 μg/mL) for 18 h and subjected to Antifungal Assay. RESULTS: Carviolin showed antifungal activity with MIC less than 200 μg/mL against all three fungi. [1]
In vivoIn a mouse model of xenograft human solid tumors, oral administration of CX-5461 (50 mg/kg) demonstrated antitumor activity against solid tumors.
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information0.1 M HCl : 25 mg/mL (48.68 mM), Sonictaion and heating are recommended.
DMSO : 1 mg/mL (1.95 mM), Sonication is recommended.
H2O : 5.15 mg/mL (10.03 mM), when pH is adjusted to 7 with HCl. Sonication is recommended.
KeywordsRNASynthesis | RNA Synthesis | Pol I-driven transcription of rRNA | Inhibitor | inhibit | DNASynthesis | DNA/RNA Synthesis | DNA Synthesis | CX-5461 | CX5461 | CX 5461
Inhibitors Related5-Fluorouracil | Adenine hemisulfate | Erythromycin thiocyanate | Guanidine hydrochloride | Hexane-1,6-diol | 1,4-Naphthoquinone | Adenine | Vidarabine | Carbazole | Thymidine | Docosanoic acid | Usnic Acid
Related Compound LibrariesHighly Selective Inhibitor Library | Bioactive Compound Library | ReFRAME Related Library | Anti-Breast Cancer Compound Library | Anti-Cancer Clinical Compound Library | Drug Repurposing Compound Library | Inhibitor Library | Anti-Aging Compound Library | Bioactive Compounds Library Max | Cell Cycle Compound Library | Anti-Cancer Drug Library | Anti-Cancer Active Compound Library

Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

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TargetMol Chemicals Inc.

6YR United StatesUnited States
  • Since: 2011-01-07
  • Address: 36 Washington Street, Wellesley Hill, MA
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