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LRK-4189

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Catalog No. T210497Cas No. 3063346-83-5

LRK-4189 is an orally active and highly selective PIP4K2C PROTAC degrader. In MOLT-4 cells, its DC₅₀ for PIP4K2C is lower than 500 nM. This compound exhibits significant anti-tumor effects, inducing endogenous apoptosis in cells and activating the interferon signaling pathway, thereby triggering immune-mediated tumor cell killing in immunologically inert microsatellite stable (MSS) colorectal cancer (CRC) cells. Therefore, LRK-4189 can be used to study the molecular mechanisms and treatment strategies of MSS-type colorectal cancer and related cancers.

LRK-4189

LRK-4189

😃Good
Catalog No. T210497Cas No. 3063346-83-5
LRK-4189 is an orally active and highly selective PIP4K2C PROTAC degrader. In MOLT-4 cells, its DC₅₀ for PIP4K2C is lower than 500 nM. This compound exhibits significant anti-tumor effects, inducing endogenous apoptosis in cells and activating the interferon signaling pathway, thereby triggering immune-mediated tumor cell killing in immunologically inert microsatellite stable (MSS) colorectal cancer (CRC) cells. Therefore, LRK-4189 can be used to study the molecular mechanisms and treatment strategies of MSS-type colorectal cancer and related cancers.
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Product Introduction

Bioactivity
Description
LRK-4189 is an orally active and highly selective PIP4K2C PROTAC degrader. In MOLT-4 cells, its DC₅₀ for PIP4K2C is lower than 500 nM. This compound exhibits significant anti-tumor effects, inducing endogenous apoptosis in cells and activating the interferon signaling pathway, thereby triggering immune-mediated tumor cell killing in immunologically inert microsatellite stable (MSS) colorectal cancer (CRC) cells. Therefore, LRK-4189 can be used to study the molecular mechanisms and treatment strategies of MSS-type colorectal cancer and related cancers.
Chemical Properties
Molecular Weight793.9
FormulaC43H49F2N9O4
Cas No.3063346-83-5
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
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.
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