Abstract
The title compounds were synthesized in optically pure form from L-quebrachitol via the known 3-homologated inositol derivative 1; also prepared were D-3-deoxy-3-methylene-, -3-(hydroxymethyl)-, and -3-(iodomethyl)-myo-inositol. None of these compounds significantly inhibited the growth of wild type and v-sis-transformed NIH 3T3 cells at millimolar concentration.
Original language | English (US) |
---|---|
Pages (from-to) | 1323-1326 |
Number of pages | 4 |
Journal | Bioorganic and Medicinal Chemistry Letters |
Volume | 3 |
Issue number | 6 |
DOIs | |
State | Published - Jun 1993 |
Externally published | Yes |
ASJC Scopus subject areas
- Biochemistry
- Molecular Medicine
- Molecular Biology
- Pharmaceutical Science
- Drug Discovery
- Clinical Biochemistry
- Organic Chemistry