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AMC-3-030

Catalog No. T215007 Copy Product Info
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AMC-3-030 is a selective and potent dual inhibitor targeting HDAC6 and chymotrypsin-like proteasome, with IC50 values of 884 nM and 4.17 nM, respectively. It inhibits cell proliferation and reduces levels of α-tubulin and β-actin. AMC-3-030 is applicable in the research of multiple myeloma.

AMC-3-030

Copy Product Info
🥰Excellent
Catalog No. T215007

AMC-3-030 is a selective and potent dual inhibitor targeting HDAC6 and chymotrypsin-like proteasome, with IC50 values of 884 nM and 4.17 nM, respectively. It inhibits cell proliferation and reduces levels of α-tubulin and β-actin. AMC-3-030 is applicable in the research of multiple myeloma.

AMC-3-030
Cas No. 2926656-07-5
Pack SizePriceUSA StockGlobal StockQuantity
10 mgInquiry10-14 weeks10-14 weeks
50 mgInquiry10-14 weeks10-14 weeks
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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With extensive experience in compound synthesis, we can provide rapid custom synthesis services for this product according to your research needs.
For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
AMC-3-030 is a selective and potent dual inhibitor targeting HDAC6 and chymotrypsin-like proteasome, with IC50 values of 884 nM and 4.17 nM, respectively. It inhibits cell proliferation and reduces levels of α-tubulin and β-actin. AMC-3-030 is applicable in the research of multiple myeloma.
Targets&IC50
HDAC6:884 nM
In vitro
AMC-3-030 exhibits inhibitory effects on the proliferation of RPMI-8226 cells, with an IC 50 value of 4.54 μM.
Chemical Properties
Molecular Weight604.51
FormulaC32H41BN4O7
Cas No.2926656-07-5
SmilesC[C@@]12[C@]3(C(C)(C)[C@](C3)(C[C@@]1(OB([C@@H](NC(CNC(=O)C4=CC=C(C(NOC(NC5=CC=CC=C5)=O)=O)C=C4)=O)CC(C)C)O2)[H])[H])[H]
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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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:
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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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
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