From: Mechanism of action of lenalidomide in hematological malignancies
Name | Thalidomide | Lenalidomide | Pomalidomide |
---|---|---|---|
Empirical Formula | C13H10N2O4 | C13H13N3O3 | C13H11N3O4 |
Molecular weight | 258.2 | 259.3 | 273.2 |
Chemical Structural | Thalidomide has two oxo groups in Phthaloyl ring | Lenalidomide has amino group at 4th position and single oxo group in Phthaloyl ring | Pomalidomide has amino group at 4th position and two oxo groups in Phthaloyl ring |
Effects on T-cell proliferation | Thalidomide stimulates T cell proliferation and increases IFN-γ and IL-2 production | Lenalidomide is 100–1000 times more potent in stimulating T cell proliferation and IFN-γ and IL-2 production than thalidomide | Pomalidomide is similar to lenalidomide, in addition, it also enhances transcription factor T-bet, which reverts Th2 cells into Th1 like effector cells in vitro |
Adverse Effects | Thalidomide has higher incidence of side effects like sedation, neuropathy and constipation. | Lenalidomide has lower incidence of adverse effects namely sedation, constipation and neuropathy than thalidomide. | Pomalidomide has lower incidence of adverse effects like sedation, constipation and neuropathy than thalidomide. |
Teratogenecity | Thalidomide is a known teratogen. | Lenalidomide is not teratogenic in rabbit models | Pomalidomide is a known teratogen. |