For a series of acyclic and carbocyclic adenosine analogues, a close correlation was found between their inhibitory effect on murine L929 cell S-adenosylhomocysteine (AdoHcy) hydrolase and their inhibitory effects on the replication of vaccinia virus and vesicular stomatitis virus (r: 0.993 and 0.988, respectively). In terms of their increasing inhibitory action against both virus replication and AdoHcy hydrolase activity the compounds ranked as follows: (S)-9-(2,3-dihydroxypropyl)adenine less than (RS)-3-adenin-9-yl-2-hydroxypropanoic acid (isobutyl ester) less than 3-deazaneplanocin A approximately carbocyclic 3-deazaadenosine less than adenosine dialdehyde less than neplanocin A. These findings point to AdoHcy hydrolase as the target for...
The carbocyclic analog of 3-deazaadenosine (C-c3 Ado) was found to inhibit in vitro the replication ...
Several nucleoside analogues which have previously been established as broad-spectrum antiviral agen...
Two synthetic analogs of neplanocin A, which were shown in a separate study to be inhibitors of S-ad...
For a series of adenosine analogues a close correlation (r = 0.986) was found between their antivira...
S-Adenosylhomocysteine hydrolase has been recognized as the target enzyme for the antiviral activity...
Various carbocyclic analogues of adenosine, including aristeromycin (carbocyclic adenosine), carbocy...
In recent years certain aliphatic and carbocyclic adenosine analogues have been developed which are ...
A new class of acyclic adenosine analogues is described which exhibit broad-spectrum antiviral activ...
9-(trans-2',trans-3'-Dihydroxycyclopent-4'-enyl)-adenine (compound 1) and -3-deazaadenine (compound ...
9-(trans-2',trans-3'-Dihydroxycyclopent-4'-enyl)-adenine (compound 1) and -3-deazaadenine (compound ...
9-(trans-2',trans-3'-dihydroxycyclopent-4'-enyl)-adenine (DHC), a specific inhibitor of S-adenosyl-L...
(S)-9-(2,3-Dihydroxypropyl)adenine, a novel nucleoside analog, the sugar moiety of which is replaced...
In a previous report (De Clercq E, Cools M and Balzarini J, Biochem Pharmacol 38: 1771-1778, 1989) w...
Of a series of carbocyclic analogs of adenosine, in which the ribose moiety was replaced by a cyclop...
Two synthetic analogs of neplanocin A, which were shown in a separate study to be inhibitors of S-ad...
The carbocyclic analog of 3-deazaadenosine (C-c3 Ado) was found to inhibit in vitro the replication ...
Several nucleoside analogues which have previously been established as broad-spectrum antiviral agen...
Two synthetic analogs of neplanocin A, which were shown in a separate study to be inhibitors of S-ad...
For a series of adenosine analogues a close correlation (r = 0.986) was found between their antivira...
S-Adenosylhomocysteine hydrolase has been recognized as the target enzyme for the antiviral activity...
Various carbocyclic analogues of adenosine, including aristeromycin (carbocyclic adenosine), carbocy...
In recent years certain aliphatic and carbocyclic adenosine analogues have been developed which are ...
A new class of acyclic adenosine analogues is described which exhibit broad-spectrum antiviral activ...
9-(trans-2',trans-3'-Dihydroxycyclopent-4'-enyl)-adenine (compound 1) and -3-deazaadenine (compound ...
9-(trans-2',trans-3'-Dihydroxycyclopent-4'-enyl)-adenine (compound 1) and -3-deazaadenine (compound ...
9-(trans-2',trans-3'-dihydroxycyclopent-4'-enyl)-adenine (DHC), a specific inhibitor of S-adenosyl-L...
(S)-9-(2,3-Dihydroxypropyl)adenine, a novel nucleoside analog, the sugar moiety of which is replaced...
In a previous report (De Clercq E, Cools M and Balzarini J, Biochem Pharmacol 38: 1771-1778, 1989) w...
Of a series of carbocyclic analogs of adenosine, in which the ribose moiety was replaced by a cyclop...
Two synthetic analogs of neplanocin A, which were shown in a separate study to be inhibitors of S-ad...
The carbocyclic analog of 3-deazaadenosine (C-c3 Ado) was found to inhibit in vitro the replication ...
Several nucleoside analogues which have previously been established as broad-spectrum antiviral agen...
Two synthetic analogs of neplanocin A, which were shown in a separate study to be inhibitors of S-ad...