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PQ32

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Catalog No. T211751

PQ32 is an anti-tumor agent targeting c-MYCPu27 and KRASG-quadruplexes. It hinders the proliferation of tumor cells, arrests the cell cycle at the G2 phase, and induces apoptosis (apoptosis). PQ32 suppresses the expression of c-MYC and KRAS genes. It can inhibit tumor growth in mice and is applicable for research in cancers such as lymphoma, breast cancer, lung cancer, hepatocellular carcinoma, and colorectal cancer.

PQ32

PQ32

😃Good
Catalog No. T211751
PQ32 is an anti-tumor agent targeting c-MYCPu27 and KRASG-quadruplexes. It hinders the proliferation of tumor cells, arrests the cell cycle at the G2 phase, and induces apoptosis (apoptosis). PQ32 suppresses the expression of c-MYC and KRAS genes. It can inhibit tumor growth in mice and is applicable for research in cancers such as lymphoma, breast cancer, lung cancer, hepatocellular carcinoma, and colorectal cancer.
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction

Bioactivity
Description
PQ32 is an anti-tumor agent targeting c-MYCPu27 and KRASG-quadruplexes. It hinders the proliferation of tumor cells, arrests the cell cycle at the G2 phase, and induces apoptosis (apoptosis). PQ32 suppresses the expression of c-MYC and KRAS genes. It can inhibit tumor growth in mice and is applicable for research in cancers such as lymphoma, breast cancer, lung cancer, hepatocellular carcinoma, and colorectal cancer.
In vitro
PQ32 demonstrates antitumor activity against RAJI, CA46, MDA-MB-231, A549, HepG2, HT29, and HEK-293T cell lines with IC50 values of 1.75, 2.68, 1.07, 3.48, 2.72, 1.50, and 4.09 μM, respectively. PQ32 at 1.5 μM for 24 hours can induce cell cycle arrest and apoptosis in MDA-MB-231 cells. Additionally, PQ32 at concentrations ranging from 1.5 to 3 μM over 24 to 72 hours can inhibit the expression of c-MYC and KRAS genes and proteins in MDA-MB-231 cells.
In vivo
PQ32, when administered at 15 mg/kg through intratumoral injection every two days for a duration of 21 days, effectively inhibits tumor growth in HT29 xenografted nude mice.
Chemical Properties
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
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