CAS 21416-67-1|Razoxane
| Common Name | Razoxane | ||
|---|---|---|---|
| CAS Number | 21416-67-1 | Molecular Weight | 268.26900 |
| Density | 1.333g/cm3 | Boiling Point | 531.5ºC at 760mmHg |
| Molecular Formula | C11H16N4O4 | Melting Point | 193ºC |
| MSDS | USA | Flash Point | 275.3ºC |
Names
| Name | 4,4'-(Propane-1,2-diyl)bis(piperazine-2,6-dione) |
|---|---|
| Synonym | More Synonyms |
Razoxane BiologicalActivity
| Description | Razoxane (ICRF 159) is an antiangiogenic topoisomerase II inhibitor, can be used for the research of renal cell carcinoma (RCC)[1]. |
|---|---|
| Related Catalog | Research Areas >>CancerSignaling Pathways >>Cell Cycle/DNA Damage >>Topoisomerase |
| Target | Topoisomerase II |
| In Vitro | Razoxane (30 mg/kg; i.p.) exhibits antimetastatic effects in a rat osteosarcoma model. |
| In Vivo | Early treatment with Razoxane (30 mg/kg i.p. from day -2 to +14) shows a greater inhibition of pulmonary metastases than later treatment (30 mg/kg i.p. from day +14 to +28 after transplantation)[2]. Animal Model: Sprague-Dawley rats[2] Dosage: 30 mg/kg or 10 mg/kg per day Administration: Intraperitoneally (i.p.) from 2 days before to 14 days after tumor transplantation Result: Resulted in a dose-dependent prolongation of median survival time (83 or 48 days respectively, versus 38 days for the control group), but showed no influence on the growth of the primary tumor. |
| References | [1]. J P Braybrooke, et al. A phase II study of Razoxane, an antiangiogenic topoisomerase II inhibitor, in renal cell cancer with assessment of potential surrogate markers of angiogenesis. Clin Cancer Res.2000; 6(12):4697-704. [2]. F Wingen, et al. Antimetastatic effects of Razoxane in a rat osteosarcoma model. Clin Exp Metastasis.Jan-Mar 1987; 5(1):9-16. |
Chemical & Physical Properties
| Density | 1.333g/cm3 |
|---|---|
| Boiling Point | 531.5ºC at 760mmHg |
| Melting Point | 193ºC |
| Molecular Formula | C11H16N4O4 |
| Molecular Weight | 268.26900 |
| Flash Point | 275.3ºC |
| Exact Mass | 268.11700 |
| PSA | 98.82000 |
| Vapour Pressure | 1.33E-13mmHg at 25°C |
| Index of Refraction | 1.534 |
| InChIKey | BMKDZUISNHGIBY-UHFFFAOYSA-N |
| SMILES | CC(CN1CC(=O)NC(=O)C1)N1CC(=O)NC(=O)C1 |
| Storage condition | room temp |
| Water Solubility | DMSO: soluble40mg/mL |
Toxicological Information
CHEMICAL IDENTIFICATION |
ACUTE TOXICITY DATA - TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Human - woman
- DOSE/DURATION :
- 3650 mg/kg/2Y-I
- TOXIC EFFECTS :
- Kidney, Ureter, Bladder - hematuria Blood - aplastic anemia
- TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Unreported
- SPECIES OBSERVED :
- Human - woman
- DOSE/DURATION :
- 600 mg/kg/34W-I
- TOXIC EFFECTS :
- Blood - leukopenia
- TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Unreported
- SPECIES OBSERVED :
- Human - man
- DOSE/DURATION :
- 6467 mg/kg/6Y-I
- TOXIC EFFECTS :
- Blood - normocytic anemia Blood - thrombocytopenia
- TYPE OF TEST :
- LD50 - Lethal dose, 50 percent kill
- ROUTE OF EXPOSURE :
- Intraperitoneal
- SPECIES OBSERVED :
- Rodent - mouse
- DOSE/DURATION :
- 500 mg/kg
- TOXIC EFFECTS :
- Tumorigenic - active as anti-cancer agent
- TYPE OF TEST :
- TDLo - Lowest published toxic dose
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Human - man
- DOSE/DURATION :
- 693 mg/kg/77W-I
- TOXIC EFFECTS :
- Tumorigenic - Carcinogenic by RTECS criteria Blood - leukemia
- TYPE OF TEST :
- TD - Toxic dose (other than lowest)
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Human - woman
- DOSE/DURATION :
- 4650 mg/kg/2Y-C
- TOXIC EFFECTS :
- Tumorigenic - Carcinogenic by RTECS criteria Blood - leukemia
- TYPE OF TEST :
- TD - Toxic dose (other than lowest)
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Human - man
- DOSE/DURATION :
- 2693 mg/kg/3Y-C
- TOXIC EFFECTS :
- Tumorigenic - Carcinogenic by RTECS criteria Skin and Appendages - tumors
- TYPE OF TEST :
- TD - Toxic dose (other than lowest)
- ROUTE OF EXPOSURE :
- Oral
- SPECIES OBSERVED :
- Human - woman
- DOSE/DURATION :
- 3650 mg/kg/2Y-I
- TOXIC EFFECTS :
- Tumorigenic - Carcinogenic by RTECS criteria Blood - leukemia
- TYPE OF TEST :
- Micronucleus test
MUTATION DATA - TEST SYSTEM :
- Rodent - hamster
- DOSE/DURATION :
- 100 mg/kg
- REFERENCE :
- BJCAAI British Journal of Cancer. (Macmillan Press Ltd., Houndmills, Basingstoke, Hants. RG21 2XS, UK) V.1- 1947- Volume(issue)/page/year: 52,725,1985
- TEST SYSTEM :
- Rodent - hamster
- DOSE/DURATION :
- 100 mg/kg
- REFERENCE :
- BJCAAI British Journal of Cancer. (Macmillan Press Ltd., Houndmills, Basingstoke, Hants. RG21 2XS, UK) V.1- 1947- Volume(issue)/page/year: 52,725,1985
Safety Information
| RIDADR | NONH for all modes of transport |
|---|---|
| RTECS | TL6389900 |
Articles30
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| Development of a phospholipidosis database and predictive quantitative structure-activity relationship (QSAR) models. Toxicol. Mech. Methods 18 , 217-27, (2008) ABSTRACT Drug-induced phospholipidosis (PL) is a condition characterized by the accumulation of phospholipids and drug in lysosomes, and is found in a variety of tissue types. PL is frequently manifes... | |
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Synonyms
| 4,4'-propylenebis(piperazine-2,6-dione) |
| 4,4'-Propane-1,2-diyldipiperazine-2,6-dione |
| 4,4'-(1-Methylethylene)bis(2,6-piperazinedione) |
| dl-1,2-bis(3,5-dioxopiperazin-1-yl)-propane |
| Propyliminum |
| RAZOXANUM |
| 1,2-bis(3,5-dioxopiperazin-1-yl)-propane |
| (+)-1,2-bis(3,5-dioxopiperazinyl)propane |
| (+)-1,2-bis(3,5-dioxopiperazinyl-1-yl)propane |
| Razoxane |
