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| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
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M339846-10mg
|
10mg |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
|
$14.90
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M339846-25mg
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25mg |
3
|
$28.90
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|
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M339846-100mg
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100mg |
5
|
$94.90
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M339846-250mg
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250mg |
5
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$159.90
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M339846-1g
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1g |
5
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$459.90
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a type II topoisomerase inhibitor
| Synonyms | L01DB07 | 5,8-Bis((2-((2-hydroxyethyl)amino)ethyl)amino)-1,4-dihydroxyanthraquinone | HMS2090D05 | 1,4-dihydroxy-5,8-bis((2-((2-hydroxyethyl)amino)ethyl)amino)anthracene-9,10-dione | DTXSID4046947 | Mitoxanthrone | 1,4-DIHYDROXY-5,8-BIS((2-((2-HYDROXYETHY |
|---|---|
| Specifications & Purity | Moligand™, ≥97% |
| Storage Temp | Protected from light,Store at -20°C |
| Shipped In |
Ice chest + Ice pads This product requires cold chain shipping. Ground and other economy services are not available. |
| Grade | Moligand™ |
| Action Type | INHIBITOR |
| Mechanism of action | Inhibitor of DNA topoisomerase II alpha |
| Product Description |
Mitoxantrone is a DNA intercalating drug that inhibits DNA synthesis and is used as an anti-cancer agent. Mitoxantrone is an inhibitor of Topo II. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Anthracenes |
| Subclass | Anthraquinones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Anthraquinones |
| Alternative Parents | Aryl ketones Secondary alkylarylamines 1-hydroxy-2-unsubstituted benzenoids Vinylogous amides Vinylogous acids 1,2-aminoalcohols Dialkylamines Primary alcohols Organopnictogen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | 9,10-anthraquinone - Anthraquinone - Aryl ketone - 1-hydroxy-2-unsubstituted benzenoid - Secondary aliphatic/aromatic amine - Vinylogous acid - Vinylogous amide - 1,2-aminoalcohol - Ketone - Secondary amine - Secondary aliphatic amine - Alkanolamine - Organic oxide - Organopnictogen compound - Primary alcohol - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Organic nitrogen compound - Amine - Alcohol - Hydrocarbon derivative - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as anthraquinones. These are organic compounds containing either anthracene-9,10-quinone, 1,4-anthraquinone, or 1,2-anthraquinone. |
| External Descriptors | hydroxyanthraquinones |
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| pKa | pKa: 7.08 (Predicted), pKa: 9.27 (Predicted) |
|---|---|
| Ki Data | mAChR M2: Ki= 77.9 nM (human); mAChR M4: Ki= 89.8 nM (human); mAChR M1: Ki= 0.18 μM (human); SR-2C: Ki= 1.87 μM (human); HERG: Ki= 2.94 μM (human) |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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| Pubchem Sid | 488179822 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488179822 |
| IUPAC Name | 1,4-dihydroxy-5,8-bis[2-(2-hydroxyethylamino)ethylamino]anthracene-9,10-dione |
| INCHI | InChI=1S/C22H28N4O6/c27-11-9-23-5-7-25-13-1-2-14(26-8-6-24-10-12-28)18-17(13)21(31)19-15(29)3-4-16(30)20(19)22(18)32/h1-4,23-30H,5-12H2 |
| InChIKey | KKZJGLLVHKMTCM-UHFFFAOYSA-N |
| Smiles | C1=CC(=C2C(=C1NCCNCCO)C(=O)C3=C(C=CC(=C3C2=O)O)O)NCCNCCO |
| Isomeric SMILES | C1=CC(=C2C(=C1NCCNCCO)C(=O)C3=C(C=CC(=C3C2=O)O)O)NCCNCCO |
| RTECS | CB5748500 |
| Molecular Weight | 444.48 |
| Beilstein | 2795126 |
| Reaxy-Rn | 2795126 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2795126&ln= |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Mar 10, 2025 | M339846 | |
| Certificate of Analysis | Mar 10, 2025 | M339846 | |
| Certificate of Analysis | Mar 10, 2025 | M339846 | |
| Certificate of Analysis | Mar 08, 2024 | M339846 | |
| Certificate of Analysis | Feb 05, 2024 | M339846 | |
| Certificate of Analysis | Feb 05, 2024 | M339846 | |
| Certificate of Analysis | Feb 05, 2024 | M339846 | |
| Certificate of Analysis | Feb 05, 2024 | M339846 | |
| Certificate of Analysis | Feb 05, 2024 | M339846 | |
| Certificate of Analysis | Feb 05, 2024 | M339846 | |
| Certificate of Analysis | Feb 05, 2024 | M339846 | |
| Certificate of Analysis | Feb 05, 2024 | M339846 | |
| Certificate of Analysis | Feb 05, 2024 | M339846 | |
| Certificate of Analysis | Jan 05, 2023 | M339846 | |
| Certificate of Analysis | Jan 05, 2023 | M339846 | |
| Certificate of Analysis | Jan 05, 2023 | M339846 | |
| Certificate of Analysis | Jan 05, 2023 | M339846 | |
| Certificate of Analysis | Jan 05, 2023 | M339846 | |
| Certificate of Analysis | Jan 05, 2023 | M339846 | |
| Certificate of Analysis | Jan 05, 2023 | M339846 | |
| Certificate of Analysis | Jan 05, 2023 | M339846 | |
| Certificate of Analysis | Jan 05, 2023 | M339846 | |
| Certificate of Analysis | Jan 05, 2023 | M339846 | |
| Certificate of Analysis | Jan 05, 2023 | M339846 |
| Solubility | Slightly soluble in (methanol); insoluble in (water, acetone, chloroform) |
|---|---|
| Sensitivity | Light and heat sensitive |
| Refractive Index | n20D1.71 |
| Boil Point(°C) | ~805.7° C at 760 mmHg (Predicted) |
| Melt Point(°C) | 170-174° C |
| Molecular Weight | 444.500 g/mol |
| XLogP3 | 1.000 |
| Hydrogen Bond Donor Count | 8 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 12 |
| Exact Mass | 444.201 Da |
| Monoisotopic Mass | 444.201 Da |
| Topological Polar Surface Area | 163.000 Ų |
| Heavy Atom Count | 32 |
| Formal Charge | 0 |
| Complexity | 571.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
Starting at $9.90
Starting at $45.90
| 1. Zhi Li, Shuhua Han. (2022) A Chemosensor of 1,8-Dihydroxyanthraquinone PMOs Prepared in a Ternary Deep Eutectic Solvent for the Sensitive Detection of Cu2+. ACS Omega, 7 (26): (22613–22625). |
| 2. Chunli Lou, Xiongzhen Ye, Ge Chen, Jidong Zhu, Jingwu Kang. (2021) Screening inhibitors for blocking UHRF1-methylated DNA interaction with capillary electrophoresis. JOURNAL OF CHROMATOGRAPHY A, 1636 (461790). |
| 3. Tao Xiaojun, Tao Ting, Wen Yi, Yi Jiajin, He Lihua, Huang Zixuan, Nie Yu, Yao Xiaoyan, Wang Yingying, He Chunlian, Yang Xiaoping. (2018) Novel Delivery of Mitoxantrone with Hydrophobically Modified Pullulan Nanoparticles to Inhibit Bladder Cancer Cell and the Effect of Nano-drug Size on Inhibition Efficiency. Nanoscale Research Letters, 13 (1): (1-12). |
| 4. Qianyu Xu, Haoyang Fu, Jiyuan Gu, Liyu Lei, Lan Ling. (2025) Catalytic detoxification of mitoxantrone by graphitic carbon nitride (g-C3N4) supported Fe/Pd bimetallic nanoparticles. Journal of Environmental Sciences, 148 (614). |
| 5. Tao Yanru, Zhao Hua, Xiang Yujie, Li Jin, Li Yanting, Hu Jiangling, Wang Hongmei, Jiang Xinhui. (2024) Development and Validation of a New High-Performance Liquid Chromatography-Ultraviolet Assay for Quantification of Mitoxantrone in Plasma of BALB/c-nu Mice. JOURNAL OF CHROMATOGRAPHIC SCIENCE, |
| 6. Yixuan Zhao, Jiahui Zhao, Shuqin Liu, Dunqing Wang, Jian Liu, Fei Zhang, Xiangshu Chen. (2024) Melamine enhancing Cu-Fenton reaction for degradation of anthracyclines. JOURNAL OF HAZARDOUS MATERIALS, 480 (136035). |
| 7. Haiying Liu, Yuqi Liu, Xiaoxi Lin, Jianhui Fan, Zhao Huang, Ao Li. (2024) Mitoxantrone attenuates lipopolysaccharide-induced acute lung injury via inhibition of NEDD8 activating enzyme. INTERNATIONAL IMMUNOPHARMACOLOGY, 143 (113605). |
| 8. Hongjie Zhang, Rui Geng, Benyan Zheng, Jing Wang, Yuan Hu, Xiaopeng Ma. (2025) Ultrasound-Enhanced Mitochondrial Targeting for Synergistic Mitoxantrone-Based Nanotherapy in Triple-Negative Breast Cancer. ACS Applied Nano Materials, 8 (5): (2382-2392). |