Anti‐HIV‐1 activity of 3‐deaza‐adenosine analogs: Inhibition of S‐adenosylhomocysteine hydrolase and nucleotide congeners

RK Gordon, K Ginalski, WR Rudnicki… - European journal of …, 2003 - Wiley Online Library
RK Gordon, K Ginalski, WR Rudnicki, L Rychlewski, MC Pankaskie, JM Bujnicki, PK Chiang
European journal of biochemistry, 2003Wiley Online Library
Eight adenosine analogs, 3‐deaza‐adenosine (DZA), 3‐deaza‐(±) aristeromycin (DZAri),
2′, 3′‐dideoxy‐adenosine (ddAdo), 2′, 3′‐dideoxy‐3‐deaza‐adenosine (ddDZA), 2′,
3′‐dideoxy‐3‐deaza‐(±) aristeromycin (ddDZAri), 3‐deaza‐5′‐(±) noraristeromycin
(DZNAri), 3‐deaza‐neplanocin A (DZNep), and neplanocin A (NepA), were tested as
inhibitors of human placenta S‐adenosylhomocysteine (AdoHcy) hydrolase. The order of
potency for the inhibition of human placental AdoHcy hydrolase was: DZNep≈ NepA>> …
Eight adenosine analogs, 3‐deaza‐adenosine (DZA), 3‐deaza‐(±)aristeromycin (DZAri), 2′,3′‐dideoxy‐adenosine (ddAdo), 2′,3′‐dideoxy‐3‐deaza‐adenosine (ddDZA), 2′,3′‐dideoxy‐3‐deaza‐(±)aristeromycin (ddDZAri), 3‐deaza‐5′‐(±)noraristeromycin (DZNAri), 3‐deaza‐neplanocin A (DZNep), and neplanocin A (NepA), were tested as inhibitors of human placenta S‐adenosylhomocysteine (AdoHcy) hydrolase. The order of potency for the inhibition of human placental AdoHcy hydrolase was: DZNep ≈ NepA >> DZAri ≈ DZNAri > DZA >> ddAdo ≈ ddDZA ≈ ddDZAri. These same analogs were examined for their anti‐HIV‐1 activities measured by the reduction in p24 antigen produced by 3′‐azido‐3′‐deoxythymidine (AZT)‐sensitive HIV‐1 isolates, A012 and A018, in phytohemagglutinin‐stimulated peripheral blood mononuclear (PBMCs) cells. Interestingly, DZNAri and the 2′,3′‐dideoxy 3‐deaza‐nucleosides (ddAdo, ddDZAri, and ddDZA) were only marginal inhibitors of p24 antigen production in HIV‐1 infected PBMC. DZNAri is unique because it is the only DZA analog with a deleted methylene group that precludes anabolic phosphorylation. In contrast, the other analogs were potent inhibitors of p24 antigen production by both HIV‐1 isolates. Thus it was postulated that these nucleoside analogs could exert their antiviral effect via a combination of anabolically generated nucleotides (with the exception of DZNAri), which could inhibit reverse transcriptase or other viral enzymes, and the inhibition of viral or cellular methylation reactions. Additionally, QSAR‐like models based on the molecular mechanics (MM) were developed to predict the order of potency of eight adenosine analogs for the inhibition of human AdoHcy hydrolase. In view of the potent antiviral activities of the DZA analogs, this approach provides a promising tool for designing and screening of more potent AdoHcy hydrolase inhibitors and antiviral agents.
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