Weight | 155.197 g/mol |
---|---|
Formula | C8H13NO2 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
Heliotridine (520-63-8)
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- Synthesis of optically active pyrrolizidinediols: (+)-heliotridine (Journal of the American Chemical Society, 1983)
- Free radical cyclizations in alkaloid synthesis: (+)-heliotridine and (+)-hastanecine (Tetrahedron, 1985)
- Metabolic Conversion of Heliotridine-Based Pyrrolizidine Alkaloids to Dehydroheliotridine (Molecular Pharmacology, 1970)
- Synthetic studies on pyrrolizidine alkaloids. 1. ()-Heliotridine and ()-retronecine via intramolecular dienophile transfer [8] (Journal of the American Chemical Society, 1980)
- Nuclear magnetic resonance spectra of pyrrolizidine alkaloids. I. The spectra of retronecine and heliotridine (Australian Journal of Chemistry, 1965)
- Formation of DHP-derived DNA adducts from metabolic activation of the prototype heliotridine-type pyrrolizidine alkaloid, lasiocarpine (Cancer Letters, 2006)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CN2CC=C(C2C1O)CO
-
InChIKeyHJSJELVDQOXCHO-UHFFFAOYSA-N
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