Introduction:Basic information about CAS 69408-81-7|Amonafide, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Amonafide |
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| CAS Number | 69408-81-7 | Molecular Weight | 283.325 |
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| Density | 1.3±0.1 g/cm3 | Boiling Point | 500.2±35.0 °C at 760 mmHg |
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| Molecular Formula | C16H17N3O2 | Melting Point | 162-164ºC |
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| MSDS | / | Flash Point | 256.3±25.9 °C |
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Names
| Name | 5-amino-2-[2-(dimethylamino)ethyl]benzo[de]isoquinoline-1,3-dione |
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| Synonym | More Synonyms |
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Amonafide BiologicalActivity
| Description | Amonafide is a topoisomerase II inhibitor and DNA intercalator that induces apoptotic signaling by blocking the binding of Topo II to DNA. |
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| Related Catalog | Research Areas >>Cancer |
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| Target | Topoisomerase II |
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| In Vitro | Amonafide is a topoisomerase II inhibitor and DNA intercalator that induces apoptotic signaling by blocking the binding of Topo II to DNA[1]. Amonafide produces protein-associated DNA cleavage, single-strand breaks (SSB) and DPC and DNA double-strand cleavage. Amonafide (Nafidimide, 400 nM-2.4 μM) reduces the colony-forming ability of the leukemic cell lines in a dose-dependent manner[2]. Amonafide (0.05-0.4 μg/mL) reduces several tumor growth. However, Amonafide is active against only 12% of tumors compared with standard agents (5-fluorouracil, mitomycin C, cisplatin, and etoposide), which are active against more than 40% of tumors in the human bone marrow inhibitory range[3]. Amonafide inhibits the growth of HT-29, HeLa, and PC-3 cell lines, with IC50s of 4.67, 2.73, and 6.38 μM[4]. |
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| Cell Assay | In experiments measuring survival following 1 h drug treatments, 2 × 106cells are resuspended in 2 mL warm (37°C) HBSS with 5% PCS; the appropriate drug (Amonafide) level is attained with the addition of less than 50 μL. Cells are incubated for 60 min at 37°C after which 10 mL ice cold PBS is added. The cells are then centrifuged at 200 × g for 10 min at 4°C. The wash is repeated once and the cells are resuspended in HBSS with 5% PCS and added to the agar-medium mixture for assessment of surviving clonogenic cells[2]. |
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| References | [1]. Allen SL, et al. Amonafide: a potential role in treating acute myeloid leukemia. Expert Opin Investig Drugs. 2011 Jul;20(7):995-1003. [2]. Andersson BS, et al. In vitro toxicity and DNA cleaving capacity of benzisoquinolinedione (nafidimide; NSC 308847) in human leukemia. Cancer Res. 1987 Feb 15;47(4):1040-4. [3]. Ajani JA, et al. In vitro activity of amonafide against primary human tumors compared with the activity of standard agents. Invest New Drugs. 1988 Jun;6(2):79-85. |
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Chemical & Physical Properties
| Density | 1.3±0.1 g/cm3 |
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| Boiling Point | 500.2±35.0 °C at 760 mmHg |
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| Melting Point | 162-164ºC |
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| Molecular Formula | C16H17N3O2 |
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| Molecular Weight | 283.325 |
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| Flash Point | 256.3±25.9 °C |
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| Exact Mass | 283.132080 |
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| PSA | 68.33000 |
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| LogP | 0.06 |
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| Vapour Pressure | 0.0±1.3 mmHg at 25°C |
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| Index of Refraction | 1.681 |
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| InChIKey | UPALIKSFLSVKIS-UHFFFAOYSA-N |
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| SMILES | CN(C)CCN1C(=O)c2cccc3cc(N)cc(c23)C1=O |
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| Storage condition | -20°C Freezer |
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Toxicological Information
CHEMICAL IDENTIFICATION - RTECS NUMBER :
- QK5610000
- CHEMICAL NAME :
- Naphthalimide, 3-amino-N-(2-(dimethylamino)ethyl)-
- CAS REGISTRY NUMBER :
- 69408-81-7
- LAST UPDATED :
- 199612
- DATA ITEMS CITED :
- 5
- MOLECULAR FORMULA :
- C16-H17-N3-O2
- MOLECULAR WEIGHT :
- 283.36
- WISWESSER LINE NOTATION :
- T666 1A M CVNVT&&J D2N1&1 HZ
HEALTH HAZARD DATAACUTE TOXICITY DATA - TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intravenous
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 67 mg/kg
- TOXIC EFFECTS :
- Behavioral - changes in motor activity (specific assay) Lungs, Thorax, or Respiration - dyspnea Nutritional and Gross Metabolic - weight loss or decreased weight gain
- TYPE OF TEST :
- LD - Lethal dose
- ROUTE OF EXPOSURE :
- Intravenous
- SPECIES OBSERVED :
- Mammal - dog
- DOSE/DURATION :
- >18400 ug/kg
- TOXIC EFFECTS :
- Behavioral - tremor Lungs, Thorax, or Respiration - dyspnea Gastrointestinal - changes in structure or function of salivary glands
MUTATION DATA - TYPE OF TEST :
- DNA damage
- TEST SYSTEM :
- Rodent - mouse Leukocyte
- DOSE/DURATION :
- 50 umol/L
- REFERENCE :
- BCPCA6 Biochemical Pharmacology. (Pergamon Press Inc., Maxwell House, Fairview Park, Elmsford, NY 10523) V.1- 1958- Volume(issue)/page/year: 34,3845,1985
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Synonyms
| Amonifide |
| 5-amino-2-[(dimethylamine)ethyl]-1H-benz[de-]isoquinoline-1,3-(2H)-dione |
| amonafide |
| 1H-Benz[de]isoquinoline-1,3(2H)-dione, 5-amino-2-[2-(dimethylamino)ethyl]- |
| AS-1413 |
| 5-Aminomitonafide |
| Nafidimide |
| Benzisoquinolinedione |
| Quinamed |
| Amonafidum [Latin] |
| 5-Amino-2-[2-(dimethylamino)ethyl]-1H-benzo[de]isoquinoline-1,3(2H)-dione |
| 2-(2-dimethylaminoethyl)-5-aminobenzo[de]isoquinoline-1,3-dione |
| 5-amino-2-(2-(dimethylamino)ethyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione |
| Xanafide |