Synthesis and cytotoxicity of potential tumor-inhibitory analogues of trimelamol (2,4,6-tris[(hydroxymethyl)methylamino]-1,3,5-triazine) having electron-withdrawing groups in place of methyl. [electronic resource]
Producer: 19940204Description: 4195-200 p. digitalISSN:- 0022-2623
- Animals
- Antineoplastic Agents -- chemical synthesis
- Drug Stability
- Half-Life
- Humans
- Hydrogen-Ion Concentration
- Hydrolysis
- Leukemia L1210 -- drug therapy
- Lung Neoplasms -- drug therapy
- Molecular Structure
- Plasmacytoma -- drug therapy
- Rats
- Solubility
- Structure-Activity Relationship
- Triazines -- chemistry
- Tumor Cells, Cultured
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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