| scholarly article | Q13442814 |
| P356 | DOI | 10.1080/15257770.2014.975243 |
| P698 | PubMed publication ID | 25621706 |
| P2093 | author name string | Eunae Kim | |
| Joon Hee Hong | |||
| Seyeon Kim | |||
| P2860 | cites work | Chemical etiology of nucleic acid structure: the alpha-threofuranosyl-(3'-->2') oligonucleotide system | Q28137995 |
| 4'-Substituted nucleosides. 3. Synthesis of some 4'-fluorouridine derivatives | Q28319553 | ||
| Acyclic nucleotide analogues: synthesis, antiviral activity and inhibitory effects on some cellular and virus-encoded enzymes in vitro | Q28323519 | ||
| Intracellular metabolism and mechanism of anti-retrovirus action of 9-(2-phosphonylmethoxyethyl)adenine, a potent anti-human immunodeficiency virus compound | Q28323687 | ||
| Acyclic purine phosphonate analogues as antiviral agents. Synthesis and structure-activity relationships | Q28330329 | ||
| Rapid and automated tetrazolium-based colorimetric assay for the detection of anti-HIV compounds | Q28339318 | ||
| Synthesis and antiviral activity of the nucleotide analogue (S)-1-[3-hydroxy-2-(phosphonylmethoxy)propyl]cytosine | Q28342655 | ||
| The toxicity of azidothymidine (AZT) in the treatment of patients with AIDS and AIDS-related complex. A double-blind, placebo-controlled trial | Q29620805 | ||
| Synthesis and activity of a new generation of ruthenium-based olefin metathesis catalysts coordinated with 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene ligands | Q30596579 | ||
| Design and profiling of GS-9148, a novel nucleotide analog active against nucleoside-resistant variants of human immunodeficiency virus type 1, and its orally bioavailable phosphonoamidate prodrug, GS-9131. | Q36425068 | ||
| The clinical potential of the acyclic (and cyclic) nucleoside phosphonates: the magic of the phosphonate bond | Q37866422 | ||
| Design, synthesis, and antiviral activity of adenosine 5'-phosphonate analogues as chain terminators against hepatitis C virus | Q40435746 | ||
| Cidofovir and (S)-9-[3-hydroxy-(2-phosphonomethoxy)propyl]adenine are highly effective inhibitors of vaccinia virus DNA polymerase when incorporated into the template strand | Q41915115 | ||
| Synthesis of branched 9-[2-(2-phosphonoethoxy)ethyl]purines as a new class of acyclic nucleoside phosphonates which inhibit Plasmodium falciparum hypoxanthine-guanine-xanthine phosphoribosyltransferase | Q43295327 | ||
| Deoxythreosyl phosphonate nucleosides as selective anti-HIV agents | Q45175412 | ||
| 2',3'-dideoxyinosine (ddI) in patients with the acquired immunodeficiency syndrome or AIDS-related complex. A phase I trial | Q45190383 | ||
| Synthesis and anti-HIV activity of GS-9148 (2'-Fd4AP), a novel nucleoside phosphonate HIV reverse transcriptase inhibitor | Q46829481 | ||
| Synthesis of (E)-3′-Phosphonoalkenyl Modified Nucleoside Phosphonates via a Highly Stereoselective Olefin Cross-Metathesis Reaction | Q57082302 | ||
| Synthesis of 3′-O-phosphonomethyl nucleosides with an adenine base moiety | Q57082340 | ||
| Preparation of acyclo nucleoside phosphonate analogues based on cross-metathesis | Q57241293 | ||
| P433 | issue | 2 | |
| P304 | page(s) | 130-147 | |
| P577 | publication date | 2015-01-01 | |
| P1433 | published in | Nucleosides, Nucleotides & Nucleic Acids | Q7068261 |
| P1476 | title | Synthesis of novel 2',3'-difluorinated 5'-deoxythreosyl phosphonic acid nucleosides as antiviral agents | |
| P478 | volume | 34 |
Search more.