Semisynthesis and cytotoxic activities of novel oxime ester derivatives of the diterpene stemodin
Creators
- 1. Universidade Federal do Ceará (UFC), Fortaleza, CE (Brazil)
Description
Stemodin (1) is a diterpene produced by Stemodia maritima L. (Scrophulariaceae) and shows antiviral and tumor cell proliferation inhibitory activities. Chemical modifications of 1 were performed to produce the known stemodinone (2), two new stemodinone oximes, Z (3) and E (4), and seven new oxime esters derivatives (5, 6, 7, 8, 9, 10, and 11). All derivatives were evaluated for their cytotoxic activity in HL60 (promyelocytic leukemia), SNB-19 (astrocytoma), HCT-116 (colon carcinoma), and PC3 (prostate) human cancer cell lines, and L929 (healthy murine cells). Oximes 3 and 4 showed lower cytotoxic values than 1 against all cancer cell lines tested. However, esters 9 and 10 exhibited cell growth inhibition percentages higher than 1 against PC3, SNB-19, and HCT-116 cancer cell lines, ranging from 62.96 to 94.27%. Many of these values exceed that presented by doxorubicin (66.05-86.87%). All compounds showed no cytotoxic effect on healthy cells at the tested concentration of 25 μg mL-1. (author)
Additional details
Publishing Information
- Journal Title
- Journal of the Brazilian Chemical Society (Online)
- Journal Volume
- 35
- Journal Issue
- 6
- Journal Page Range
- 8 p.
- ISSN
- 1678-4790
INIS
- Country of Publication
- Brazil
- Country of Input or Organization
- Brazil
- INIS RN
- 55052640
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- ANIMAL CELLS; ANTINEOPLASTIC DRUGS; CARBON 13; FOURIER TRANSFORMATION; GROWTH; HYDROGEN 1; INFRARED SPECTRA; NMR SPECTRA; OXIMES; PLANTS; TOXICITY
- Descriptors DEC
- AMINES; CARBON ISOTOPES; DRUGS; EVEN-ODD NUCLEI; HYDROGEN ISOTOPES; HYDROXY COMPOUNDS; INTEGRAL TRANSFORMATIONS; ISOTOPES; LIGHT NUCLEI; NUCLEI; ODD-EVEN NUCLEI; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; SPECTRA; STABLE ISOTOPES; TRANSFORMATIONS