Abstract
2-Fluoro- and 2-chloroneplanocin A's (2 and 3) were synthesized as an adenosine deaminase resistant-equivalent of neplanocin A, and evaluated for their antitumor and antiviral activities. Of these, 2 was completely resistant to adenosine deaminase and showed more significant antitumor and antiviral activities than neplanocin A.
MeSH terms
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Adenosine / analogs & derivatives*
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Adenosine / chemistry
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Adenosine / metabolism
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Adenosine / pharmacology
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Adenosine / therapeutic use
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Adenosine Deaminase / metabolism*
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Animals
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Antibiotics, Antineoplastic / chemical synthesis*
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Antibiotics, Antineoplastic / chemistry
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Antibiotics, Antineoplastic / pharmacology
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Antibiotics, Antineoplastic / therapeutic use
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Antiviral Agents / chemical synthesis*
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Antiviral Agents / chemistry
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Antiviral Agents / pharmacology
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Drug Resistance
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Fibrosarcoma / drug therapy*
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Mice
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RNA Viruses / drug effects*
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Ribavirin / pharmacology
Substances
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Antibiotics, Antineoplastic
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Antiviral Agents
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Ribavirin
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neplanocin A
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Adenosine Deaminase
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Adenosine