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M9650244.TXT
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1996-03-09
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Document 0244
DOCN M9650244
TI Synthesis and antiviral effects of 2-heteroaryl substituted adenosine
and 8-heteroaryl substituted guanosine derivatives.
DT 9605
AU Persson T; Gronowitz S; Hornfeldt AB; Johansson NG; Chemical Center,
Lund, Sweden.
SO Bioorg Med Chem. 1995 Oct;3(10):1377-82. Unique Identifier : AIDSLINE
MED/96120458
AB 2-(2- and 3-Thienyl)adenosine and the corresponding furyl derivatives
were prepared though Pd(0)-catalyzed coupling of
2',3',5'-tri-O-(t-butyldimethylsilyl)-2-iodoadenosine with the
appropriate tributyltin derivatives followed by deprotection.
Preparation of the 8-(2- and 3-thienyl)guanosines and 8-(2- and
3-furyl)guanosines followed a similar route. Antiviral properties of
these compounds and the related 2,6-diaminopurine ribofuranosides were
of no pharmacological interest.
DE Adenosine/*ANALOGS & DERIVATIVES/CHEMICAL SYNTHESIS/*PHARMACOLOGY
Antiviral Agents/CHEMICAL SYNTHESIS/*PHARMACOLOGY Cell Division/DRUG
EFFECTS Cell Line Enzyme-Linked Immunosorbent Assay
Guanosine/*ANALOGS & DERIVATIVES/CHEMICAL SYNTHESIS/*PHARMACOLOGY
Herpesvirus 1, Human/DRUG EFFECTS Human HIV-1/DRUG EFFECTS Nuclear
Magnetic Resonance Orthomyxovirus Type A, Human/DRUG EFFECTS Support,
Non-U.S. Gov't Virus Replication/DRUG EFFECTS JOURNAL ARTICLE
SOURCE: National Library of Medicine. NOTICE: This material may be
protected by Copyright Law (Title 17, U.S.Code).