Abstract
There were synthesized new types of ribbon type steroidal dimers derived from three types of steroidal skeletons (cholic acid, etienic acid, estrone) using Cu(I) catalyzed 1, 3-dipolar cycloaddition reaction. Steroid parts of the molecular "ribbons" are linked by heterocyclic moiety, namely by 2,6-bis((1H-1,2,3-triazol-1-yl)-methyl)pyridine. Compounds synthesized possess different cytotoxic and hormone receptor modulating activities.
Copyright © 2013 Elsevier Inc. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Androstenes / chemistry*
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Catalysis
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Cell Line, Tumor
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Cell Survival / drug effects
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Cholic Acid / chemistry*
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Cytotoxins / chemical synthesis*
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Cytotoxins / pharmacology
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Estrone / chemistry*
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Hormone Antagonists / chemical synthesis*
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Hormone Antagonists / pharmacology
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Humans
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Molecular Structure
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Pyridines / chemistry
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Receptors, Steroid / antagonists & inhibitors
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Receptors, Steroid / metabolism
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Steroids / chemical synthesis*
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Steroids / pharmacology
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Structure-Activity Relationship
Substances
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Androstenes
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Cytotoxins
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Hormone Antagonists
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Pyridines
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Receptors, Steroid
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Steroids
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Estrone
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etienic acid
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Cholic Acid