HDAC degrader-2

Name: HDAC degrader-2
Brand: TargetMol
SKU: TYD-05018
Rating: 4.5 (1 reviews)

Catalog No. TYD-05018 Copy Product Info

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HDACdegrader-2 is a selective HDAC degrader with a DC50 value of 2.55 μM for HDAC1. It effectively induces the degradation of HDAC1 and HDAC2, without significantly affecting HDAC3, 4, 6, and 8. HDACdegrader-2 exhibits strong antiproliferative effects on MM.1S and MCF-7 cells and can induce apoptosis (apoptosis) in myeloma cells. This compound is useful for research on myeloma.

HDAC degrader-2

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Catalog No. TYD-05018

HDAC degrader-2

Pack Size	Price	USA Stock	Global Stock	Quantity
10 mg	Inquiry	Inquiry	Inquiry
50 mg	Inquiry	Inquiry	Inquiry

For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)

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For research use only—not for human use. No sales to individuals. Use as intended only.

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Product Introduction

Bioactivity

Description	HDACdegrader-2 is a selective HDAC degrader with a DC50 value of 2.55 μM for HDAC1. It effectively induces the degradation of HDAC1 and HDAC2, without significantly affecting HDAC3, 4, 6, and 8. HDACdegrader-2 exhibits strong antiproliferative effects on MM.1S and MCF-7 cells and can induce apoptosis (apoptosis) in myeloma cells. This compound is useful for research on myeloma.
Targets&IC50	HDAC1:2.55 μM (DC50)
In vitro	HDAC-degrader 2 (Compound SZ-2) exhibits significant antiproliferative activity against MM.1S cells (IC 50 = 3.28 μM) and MCF-7 cells (IC 50 = 3.46 μM) over 24 hours. Additionally, HDAC-degrader 2, at 5 μM concentration for 48 hours, markedly induces apoptosis in MM.1S cells.

Chemical Properties

Storage & Solubility Information

Storage

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

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In Vivo Formulation Calculator (Clear solution)

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:

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 DMSO TargetMol | 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 DMSO TargetMol | reagent stock solution to 400 μL PEG300 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 ddH₂O TargetMol | 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.

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You can also refer to dose conversion for different animals. More Dose Conversion

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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc