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Synthesis of simplified tedanolide analogues--connecting tedanolide to myriaporone and gephyronic acid.
- Source :
-
ChemMedChem [ChemMedChem] 2012 May; Vol. 7 (5), pp. 771-5. Date of Electronic Publication: 2012 Mar 01. - Publication Year :
- 2012
-
Abstract
- Southern belles! Simplified analogues of tedanolide, a natural product with picomolar activity against a range of tumor cell lines, were synthesized and evaluated for potency in mammalian cancer cells. The truncated analogues were found to retain significant activity in vitro (23 μmol mL(-1) for the example shown) compared with the parent compound tedanolide (0.33 nmol mL(-1)), and represent potential leads for the development of novel anticancer agents.<br /> (Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)
- Subjects :
- Alkenes chemistry
Alkenes pharmacology
Animals
Antineoplastic Agents chemical synthesis
Antineoplastic Agents chemistry
Antineoplastic Agents pharmacology
Cell Line, Tumor
Epoxy Compounds chemistry
Epoxy Compounds pharmacology
Fatty Acids, Monounsaturated chemical synthesis
Fatty Acids, Monounsaturated chemistry
Fatty Acids, Monounsaturated pharmacology
Humans
Inhibitory Concentration 50
Macrolides chemistry
Macrolides pharmacology
Mice
Molecular Structure
Neoplasms drug therapy
Alkenes chemical synthesis
Epoxy Compounds chemical synthesis
Macrolides chemical synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 1860-7187
- Volume :
- 7
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- ChemMedChem
- Publication Type :
- Academic Journal
- Accession number :
- 22383258
- Full Text :
- https://doi.org/10.1002/cmdc.201100576