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Aclacinomycin A hydrochloride

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Catalog No. T10238Cas No. 75443-99-1
Alias Aclarubicin hydrochloride

Aclacinomycin A hydrochloride (Aclarubicin HCl) is an anthracycline antibiotic and inhibitor of topoisomerase I/II, interfering with DNA transcription and replication, inhibiting tumour invasion and angiogenesis, generating reactive oxygen species (ROS), and inhibiting the catalytic centre of the 20S proteasome. It is indicated for the treatment of relapsed leukaemia and advanced malignant lymphoma.

Aclacinomycin A hydrochloride

Aclacinomycin A hydrochloride

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Catalog No. T10238Alias Aclarubicin hydrochlorideCas No. 75443-99-1
Aclacinomycin A hydrochloride (Aclarubicin HCl) is an anthracycline antibiotic and inhibitor of topoisomerase I/II, interfering with DNA transcription and replication, inhibiting tumour invasion and angiogenesis, generating reactive oxygen species (ROS), and inhibiting the catalytic centre of the 20S proteasome. It is indicated for the treatment of relapsed leukaemia and advanced malignant lymphoma.
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1 mg$453-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Appearance:Solid
Color:Orange
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Product Introduction

Bioactivity
Description
Aclacinomycin A hydrochloride (Aclarubicin HCl) is an anthracycline antibiotic and inhibitor of topoisomerase I/II, interfering with DNA transcription and replication, inhibiting tumour invasion and angiogenesis, generating reactive oxygen species (ROS), and inhibiting the catalytic centre of the 20S proteasome. It is indicated for the treatment of relapsed leukaemia and advanced malignant lymphoma.
In vitro
Method:
A cell viability assay was performed using V79 and irs-2 cell lines. Cells were treated with varying concentrations of Aclacinomycin A hydrochloride at 0, 0.006, 0.12, 1.2, and 2.4 μM for 3 hours. The effect on the catalytic activity of topoisomerase II (topo II) was evaluated.

Result:
Aclacinomycin A hydrochloride significantly inhibited topo II catalytic activity in a dose-dependent manner. Compared to the untreated group, all treated groups showed a statistically significant decrease in topo II activity, indicating that the drug effectively interferes with topo II function and subsequently affects cell viability. [2]
In vivo
Method:
P-388 leukemia cells were transplanted into DBA/2 and CDF1 (BALB/c × DBA/2) mice. Starting 3 hours after transplantation, mice received daily intraperitoneal injections of Aclacinomycin A hydrochloride for 10 consecutive days at doses of 0.75, 1.5, 3, and 6 mg/kg.

Result:
Aclacinomycin A hydrochloride significantly inhibited tumor growth in a dose-dependent manner.[3]
Animal Research
Animal Model: DBA/2, CDF1 (BALB/c×DBA/2) mice with Leukemia P-388.
Dosage: 0.75 mg/kg, 1.5 mg/kg, 3 mg/kg, 6 mg/kg.
Administration: Intraperitoneal administration daily for 10 days starting 3 hr after transplantation.
Result: Inhibited tumor growth [4].
SynonymsAclarubicin hydrochloride
Chemical Properties
Molecular Weight848.33
FormulaC42H54ClNO15
Cas No.75443-99-1
SmilesC(OC)(=O)[C@@H]1C2=C([C@@H](O[C@H]3C[C@H](N(C)C)[C@H](O[C@H]4C[C@H](O)[C@H](O[C@@H]5O[C@@H](C)C(=O)CC5)[C@H](C)O4)[C@H](C)O3)C[C@@]1(CC)O)C(O)=C6C(=C2)C(=O)C=7C(C6=O)=C(O)C=CC7.Cl
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 120 mg/mL (141.45 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (4.72 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.1788 mL5.8939 mL11.7879 mL58.9393 mL
5 mM0.2358 mL1.1788 mL2.3576 mL11.7879 mL
10 mM0.1179 mL0.5894 mL1.1788 mL5.8939 mL
20 mM0.0589 mL0.2947 mL0.5894 mL2.9470 mL
50 mM0.0236 mL0.1179 mL0.2358 mL1.1788 mL
100 mM0.0118 mL0.0589 mL0.1179 mL0.5894 mL

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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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g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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