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Antiretroviral potency of 4′-ethnyl-2′-fluoro-2′-deoxyadenosine, tenofovir alafenamide and second-generation NNRTIs across diverse HIV-1 subtypes
Author(s) -
Duncan Njenda,
Shambhu G. Aralaguppe,
Kamalendra Singh,
Rohit Rao,
Anders Sönnerborg,
Stefan G. Sarafianos,
Ujjwal Neogi
Publication year - 2018
Publication title -
journal of antimicrobial chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dky256
Subject(s) - efavirenz , etravirine , tenofovir alafenamide , rilpivirine , virology , nevirapine , reverse transcriptase , raltegravir , potency , human immunodeficiency virus (hiv) , reverse transcriptase inhibitor , chemistry , dolutegravir , deoxyadenosine , biology , dna , antiretroviral therapy , viral load , rna , biochemistry , in vitro , gene
4'-Ethnyl-2'-fluoro-2'-deoxyadenosine (EFdA) is a novel translocation-defective reverse transcriptase inhibitor. We investigated the virological and biochemical inhibitory potentials of EFdA against a broad spectrum of subtype-specific chimeric viruses and compared it with tenofovir alafenamide, nevirapine, efavirenz, rilpivirine and etravirine.

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