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Aclacinomycin A hydrochloride

SKU: orb1992962

Description

Aclarubicin hydrochloride is an anthracycline antibiotic that inhibits topoisomerase I/II and the 20S proteasome, disrupting DNA processes and generating ROS. It is used in research for studying relapsed leukemia and advanced lymphoma, with applications in both in vitro and in vivo models of oncology and cancer pharmacology.

Research Area

Cell Biology, Immunology & Inflammation, Infectious Disease & Virology, Molecular Biology, Protein Biochemistry

Images & Validation

Key Properties

CAS Number75443-99-1
MW848.33
FormulaC42H54ClNO15
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
TargetTopoisomerase,ROS,Proteasome,DNA,Antibiotic,DNA/RNA Synthesis
Solubility10% DMSO+40% PEG300+5% Tween 80+45% Saline:4 mg/mL (4.72 mM);DMSO:120 mg/mL (141.45 mM)

Bioactivity

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.
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.
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 .

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

Aclarubicin hydrochloride
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Key Properties

No computed properties available.

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Aclacinomycin A hydrochloride (orb1992962)

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% DMSO +
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% Tween 80 +
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1 mg
¥ 6,500.00
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