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Doxorubicin

Cat. No. M29508
Doxorubicin Structure
Synonym:

Hydroxydaunorubicin

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Biological Activity

Doxorubicin (Hydroxydaunorubicin), a cytotoxic anthracycline antibiotic, is an anti-cancer chemotherapy agent. Doxorubicin inhibits topoisomerase II with an IC50 of 2.67 μM, thus stopping DNA replication. Doxorubicin inhibits human DNA topoisomerase I with an IC50 of 0.8 μM. Doxorubicin reduces basal phosphorylation of AMPK and its downstream target acetyl-CoA carboxylase. Doxorubicin induces apoptosis and autophagy.

Chemical Information
Molecular Weight 543.52
Formula C27H29NO11
CAS Number 23214-92-8
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Sijongesonke Peter, et al. Molecules. Doxorubicin-Based Hybrid Compounds as Potential Anticancer Agents: A Review

[2] Lusha Zhu, et al. Anticancer Agents Med Chem. The Synthesis of Nano-Doxorubicin and its Anticancer Effect

[3] Sangeeta Rivankar. J Cancer Res Ther. An overview of doxorubicin formulations in cancer therapy

[4] Cristina Carvalho, et al. Curr Med Chem. Doxorubicin: the good, the bad and the ugly effect

[5] P A Speth, et al. Clin Pharmacokinet. Clinical pharmacokinetics of doxorubicin

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Keywords: Doxorubicin, Hydroxydaunorubicin supplier, Topoisomerase, inhibitors, activators


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