Abstract
[structure: see text]. We describe the synthesis of the first locked side-chain analogues of the natural hormone 1alpha,25-(OH)2-D3 and their effects on gene transcription in human colon cancer cells. Analogue 2 was more potent than 1alpha,25-(OH)2-D3 at inducing vitamin D receptor (VDR) transcriptional activity. Analogues 3a and 3b show potency similar to that of 1alpha,25-(OH)2-D3, whereas 3c was less active. The novel analogues efficiently bind VDR in vivo to induce transcription from a consensus vitamin D responsive element (VDRE).
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alkynes / chemistry
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Calcitriol / analogs & derivatives*
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Calcitriol / chemistry
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Calcitriol / pharmacology
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Cell Line, Tumor / drug effects
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Colonic Neoplasms / genetics
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Colonic Neoplasms / pathology
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Gene Expression Regulation, Neoplastic
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Humans
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Hydrocarbons, Aromatic / chemistry
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Luciferases / analysis
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Luciferases / genetics
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Molecular Structure
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Receptors, Calcitriol / agonists*
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Receptors, Calcitriol / physiology
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Structure-Activity Relationship
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Transcription, Genetic / drug effects*
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Vitamin D Response Element / genetics
Substances
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Alkynes
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Hydrocarbons, Aromatic
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Receptors, Calcitriol
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Luciferases
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Calcitriol