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Doxorubicin (Adriamycin) HCl is an antineoplastic agent used in the treatment of a wide range of cancers, including hematological malignancies, many types of carcinoma, and soft tissue sarcomas. Doxorubicin interacts with DNA by intercalation and inhibition of macromolecular biosynthesis. Doxorubicin stabilizes the topoisomerase II complex after it has broken the DNA chain for replication, preventing the DNA double helix from being resealed and thereby stopping the process of replication. In studies with isolated nuclei, adriamycin was also a more potent inhibitor of DNA synthesis than RNA synthesis. However, with intact cells, adriamycin inhibited both DNA and RNA synthesis to about the same extent. The inhibition produced by adriamycin on RNA synthesis in intact cells was greater than that observed in the cell-free systems. Adriamycin inhibited protein synthesis in a cell-free system consisting of polyribosomes, transfer RNA, and enzymes but did not inhibit protein synthesis in intact cells. Combination therapy experiments with sirolimus (rapamycin) and doxorubicin have shown promise in treating Akt-positive lymphomas in mice.
Clin Transl Med. 2025 May 05;15(5):e70327.
Targeting capacity, safety and efficacy of engineered extracellular vesicles delivered by transdermal microneedles to treat plasmacytoma in mice
Doxorubicin HCL purchased from AbMole
Cancer Med. 2025 Apr 14;14(8):e70785.
Blockade of Exosome Release Sensitizes Breast Cancer to Doxorubicin via Inhibiting Angiogenesis
Doxorubicin HCL purchased from AbMole
Cancer Res. 2024 May 8.
HDAC Inhibition Increases CXCL12 Secretion to Recruit Natural Killer Cells in Peripheral T Cell Lymphoma | Cancer Research | American Association for Cancer Research
Doxorubicin HCL purchased from AbMole
ACS Appl Mater Interfaces. 2024 Feb;16(6):6868-6878.
Doxorubicin-Loaded Microalgal Delivery System for Combined Chemotherapy and Enhanced Photodynamic Therapy of Osteosarcoma
Doxorubicin HCL purchased from AbMole
Phytomedicine. 2024 Jan;126:155395.
Bufalin suppresses hepatocellular carcinogenesis by targeting M2 macrophage-governed Wnt1/β-catenin signaling
Doxorubicin HCL purchased from AbMole
ACS Appl Bio Mater. 2024 Sep 06.
Doxorubicin-Loaded Ultrasmall Gold Nanoparticles (1.5 nm) for Brain Tumor Therapy and Assessment of Their Biodistribution
Doxorubicin HCL purchased from AbMole
Eng. Regen. 2024 Mar.
Microalgae-based drug delivery system for tumor microenvironment photo-modulating and synergistic chemo-photodynamic therapy of osteosarcoma
Doxorubicin HCL purchased from AbMole
Elife. 2021 Jun 28;10:e65150.
Resistance to different anthracycline chemotherapeutics elicits distinct and actionable primary metabolic dependencies in breast cancer
Doxorubicin HCL purchased from AbMole
Mol Med Rep. 2021 Mar;23(3):219.
Shengxian decoction decreases doxorubicin‑induced cardiac apoptosis by regulating the TREM1/NF‑κB signaling pathway
Doxorubicin HCL purchased from AbMole
2020 Aug.
Blockage of AMPK-ULK1 pathway mediated autophagy promotes cell apoptosis to increase doxorubicin sensitivity in breast cancer (BC) cells: an in vitro study
Doxorubicin HCL purchased from AbMole
PLoS One. 2017 Jul 13;12(7):e0181340.
Development and characterization of a human three-dimensional chondrosarcoma culture for in vitro drug testing
Doxorubicin HCL purchased from AbMole
Biomaterials. 2012 Jun;4345-52.
Antitumor efficacy following the intracellular and interstitial release of liposomal doxorubicin
Doxorubicin HCL purchased from AbMole
| Cell Experiment | |
|---|---|
| Cell lines | Human choriocarcinoma cell line |
| Preparation method | Briefly, cells were plated on 96-well plates (10,000 cells/well) and a day after (cell culture 80% confluent) were exposed to doxorubicin (0–8 mM), L-DOX (0–8 mM) or PL-DOX (0–200 mM) in non-supplemented serum-free growth medium for 4 h. After exposure, the cells were washed and further incubated for 20 h. |
| Concentrations | 0–8 µM |
| Incubation time | 24 h |
| Animal Experiment | |
|---|---|
| Animal models | Male Sprague-Dawley rats |
| Formulation | |
| Dosages | 4 mg/kg |
| Administration | i.v. |
| Molecular Weight | 579.98 |
| Formula | C27H29NO11.HCl |
| CAS Number | 25316-40-9 |
| Solubility (25°C) | DMSO 45 mg/mL Water 30 mg/mL |
| Storage | 2-8°C, protect from light, dry, sealed |
| Related Animal Modeling Products |
|---|
| Streptozotocin
Streptozotocin (STZ) is a kind of glucosamine - nitrosourea derivative. *The compound is unstable in solutions, freshly prepared is recommended |
| Bleomycin sulfate
Bleomycin sulfate (Blenoxane) is a glycopeptide antitumor antibiotic isolated from Streptomyces verticillus. |
| Loperamide hydrochloride
Loperamide hydrochloride is a high affinity μ-opioid receptor agonist with peripheral selectivity with Ki values of 2, 48 and 1156 nM for μ-, δ- and κ-opioid receptors respectively. Loperamide hydrochloride is also a selective and competitive human intestinal carboxylesterases (hiCE) inhibitor. It can be used to construct animal models of functional constipation. |
| Imiquimod
Imiquimod (R837), an imidazoquinoline amine analog to guanosine, is a selective toll like receptor 7 (TLR7) agonist. with potent indirect antiviral activity. |
| Benzbromarone
Benzbromarone is a URAT1 inhibitor that inhibits MDCKII cells over-expressing URAT1 with an IC50 of 0.190 μM. |
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Products are for research use only. Not for human use. We do not sell to patients.
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