mafosfamide has been researched along with aldophosphamide in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (100.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Maki, PA; Sladek, NE | 2 |
| Rekha, GK; Sladek, NE; Sreerama, L | 1 |
3 other study(ies) available for mafosfamide and aldophosphamide
| Article | Year |
|---|---|
Potentiation of the cytotoxic action of mafosfamide by N-isopropyl-p-formylbenzamide, a metabolite of procarbazine.
Topics: Aldehyde Dehydrogenase; Animals; Antineoplastic Agents; Cell Survival; Colony-Forming Units Assay; Cyclophosphamide; Drug Synergism; Hematopoietic Stem Cells; Inactivation, Metabolic; Kinetics; Leukemia L1210; Leukemia P388; Male; Mice; Mice, Inbred BALB C; Phosphoramide Mustards; Procarbazine | 1991 |
Intrinsic cellular resistance to oxazaphosphorines exhibited by a human colon carcinoma cell line expressing relatively large amounts of a class-3 aldehyde dehydrogenase.
Topics: Aldehyde Dehydrogenase; Chloral Hydrate; Chloromercuribenzoates; Colonic Neoplasms; Cyclophosphamide; Disulfiram; Electrophoresis, Polyacrylamide Gel; Humans; Isoelectric Focusing; p-Chloromercuribenzoic Acid; Phosphoramide Mustards; Tumor Cells, Cultured | 1994 |
Sensitivity of aldehyde dehydrogenases in murine tumor and hematopoietic progenitor cells to inhibition by chloral hydrate as determined by the ability of chloral hydrate to potentiate the cytotoxic action of mafosfamide.
Topics: Aldehyde Dehydrogenase; Animals; Cell Line; Cell Survival; Chloral Hydrate; Colony-Forming Units Assay; Cyclophosphamide; Drug Synergism; Hematopoietic Stem Cells; Humans; Mice; Mice, Inbred BALB C; Phosphoramide Mustards; Tumor Cells, Cultured | 1993 |