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ZXH-1-161 TFA

(Synonyms: ZXH-1-161 TFA (2407654-51-5 free base)) Copy Product Info
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Synonyms: ZXH-1-161 TFA (2407654-51-5 free base)

Catalog No. T63010L Copy Product Info
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ZXH-1-161 TFA is a potent small molecule degrader that functions as a modulator of the Cereblon (CRBN) E3 ubiquitin ligase and targets the degradation of the GSPT1 protein, demonstrating anti-tumor potential in multiple myeloma (MM1.S cell line) research. ZXH-1-161 TFA inhibits the STAT3 signaling pathway, effectively suppressing tumor cell proliferation and inducing apoptosis. As an important tool compound in the field of molecular glues, ZXH-1-161 is commonly used in research related to targeted protein degradation and cancer mechanisms.
ZXH-1-161 TFA
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Product Introduction

Bioactivity
Description
ZXH-1-161 TFA is a potent small molecule degrader that functions as a modulator of the Cereblon (CRBN) E3 ubiquitin ligase and targets the degradation of the GSPT1 protein, demonstrating anti-tumor potential in multiple myeloma (MM1.S cell line) research. ZXH-1-161 TFA inhibits the STAT3 signaling pathway, effectively suppressing tumor cell proliferation and inducing apoptosis. As an important tool compound in the field of molecular glues, ZXH-1-161 is commonly used in research related to targeted protein degradation and cancer mechanisms.
In vitro
ZXH-1-161 TFA(0–50 µM; 48 h) exhibited CRBN-dependent antiproliferative activity in MM1.S wild-type cells, with an IC₅₀ of 0.039 µM [1].
ZXH-1-161 TFA(0.01–10 µM; 4 h) induces GSPT1 degradation in MM1.S cells [1].
SynonymsZXH-1-161 TFA (2407654-51-5 free base)
Chemical Properties
Molecular Weight582.54
FormulaC28H25F3N6O5
SmilesO=C1NC(C(CC1)N2C(C3=C(C2)C(NC4=NC(NC5=CC=C6C(CCC6)=C5)=NC=C4)=CC=C3)=O)=O.O=C(C(F)(F)F)O
Storage & Solubility Information
StorageKeep away from direct sunlight Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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Dose Conversion

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Related Tags: ZXH-1-161 TFA chemical structure | ZXH-1-161 TFA in vitro | ZXH-1-161 TFA formula | ZXH-1-161 TFA molecular weight