Abstract
Two series of cytotoxic (IC50, K562 cell line, 1-24 μM) α-aminomethyl substituted lactones 3 and 4 were prepared by stereoselective Michael-type addition of amines to alantolactone (1) and isoalantolactone (2). The lactones 1 and 2 and their amine adducts induce apoptosis and act as alkylating agents. © 2001 Elsevier Science Ltd.
| Original language | English |
|---|---|
| Pages (from-to) | 429-431 |
| Number of pages | 2 |
| Journal | Bioorganic and Medicinal Chemistry Letters |
| Volume | 11 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 12 Feb 2001 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Cytotoxic agents (prepn. and cytotoxic activity of Michael-type amine adducts of alantolactone and isoalantolactone); Amines Role: RCT (Reactant), RACT (Reactant or reagent) (prepn. and cytotoxic activity of Michael-type amine adducts of alantolactone and isoalantolactone); Crystal structure; Molecular structure (prepn. and properties of Michael-type amine adduct of isoalantolactone); Michael reaction (stereoselective; prepn. and cytotoxic activity of Michael-type amine adducts of alantolactone and isoalantolactone)
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