These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
125 related articles for article (PubMed ID: 1588565)
1. Synthesis and anti-HIV activity of 9-[c-4,t-5-bis(hydroxymethyl)cyclopent-2-en-r-1-yl]-9H-adenine. Katagiri N; Nomura M; Sato H; Kaneko C; Yusa K; Tsuruo T J Med Chem; 1992 May; 35(10):1882-6. PubMed ID: 1588565 [TBL] [Abstract][Full Text] [Related]
2. Synthesis of purine bases having a di(hydroxymethyl)cyclopentenyl group by means of high-pressure reaction and their anti-HIV activity. Katagiri N; Nomura M; Sato H; Tameda C; Kurimoto A; Arai S; Toyota A; Kaneko C Nucleic Acids Symp Ser; 1991; (25):5-6. PubMed ID: 1842092 [TBL] [Abstract][Full Text] [Related]
3. Synthesis and antiviral activities of carbocyclic oxetanocin analogues. Maruyama T; Sato Y; Horii T; Shiota H; Nitta K; Shirasaka T; Mitsuya H; Honjo M Chem Pharm Bull (Tokyo); 1990 Oct; 38(10):2719-25. PubMed ID: 1963811 [TBL] [Abstract][Full Text] [Related]
4. Remarkable acceleration for the deamination of carbocyclic purine nucleosides by adenosine deaminase under high-pressure. Katagiri N; Shiraishi T; Toyota A; Sato H; Kaneko C Nucleic Acids Symp Ser; 1993; (29):95-6. PubMed ID: 8247811 [TBL] [Abstract][Full Text] [Related]
5. Synthesis of novel 2'-methyl carbovir analogues as potent antiviral agents. Hong JH Arch Pharm Res; 2007 Feb; 30(2):131-7. PubMed ID: 17366731 [TBL] [Abstract][Full Text] [Related]
6. Resolution of 9-(c-4,t-5-bishydroxymethylcyclopent-2-en-r-1-yl)-9H-adenine and selective inhibition of human immunodeficiency virus by the (-) enantiomer. Katagiri N; Shiraishi T; Sato H; Toyota A; Kaneko C; Yusa K; Oh-hara T; Tsuruo T Biochem Biophys Res Commun; 1992 Apr; 184(1):154-9. PubMed ID: 1567421 [TBL] [Abstract][Full Text] [Related]
7. Synthesis and anti-HIV activity of carbovir and related carbocyclic nucleosides. Vince R Nucleic Acids Symp Ser; 1991; (25):193-4. PubMed ID: 1842080 [TBL] [Abstract][Full Text] [Related]
8. A ring-enlarged oxetanocin A analogue as an inhibitor of HIV infectivity. Tseng CK; Marquez VE; Milne GW; Wysocki RJ; Mitsuya H; Shirasaki T; Driscoll JS J Med Chem; 1991 Jan; 34(1):343-9. PubMed ID: 1992135 [TBL] [Abstract][Full Text] [Related]
10. Synthesis, antiviral activity, and mechanism of drug resistance of D- and L-2',3'-didehydro-2',3'-dideoxy-2'-fluorocarbocyclic nucleosides. Wang J; Jin Y; Rapp KL; Bennett M; Schinazi RF; Chu CK J Med Chem; 2005 Jun; 48(11):3736-48. PubMed ID: 15916425 [TBL] [Abstract][Full Text] [Related]
11. Conformationally locked nucleoside analogues. Synthesis of dideoxycarbocyclic nucleoside analogues structurally related to neplanocin C. Rodriguez JB; Marquez VE; Nicklaus MC; Mitsuya H; Barchi JJ J Med Chem; 1994 Sep; 37(20):3389-99. PubMed ID: 7932567 [TBL] [Abstract][Full Text] [Related]
12. A new and short convergent synthetic strategy to carbocyclic nucleosides. Reichardt B; Meier C Nucleosides Nucleotides Nucleic Acids; 2007; 26(8-9):935-7. PubMed ID: 18058512 [TBL] [Abstract][Full Text] [Related]
13. Synthesis and anti-HIV activity of carbocyclic 2',3'-didehydro-2',3'-dideoxy 2,6-disubstituted purine nucleosides. Vince R; Hua M J Med Chem; 1990 Jan; 33(1):17-21. PubMed ID: 2296018 [TBL] [Abstract][Full Text] [Related]
14. Synthesis and antiviral activity of carbocyclic oxetanocin analogues (C-OXT-A, C-OXT-G) and related compounds. II. Maruyama T; Hanai Y; Sato Y; Snoeck R; Andrei G; Hosoya M; Balzarini J; De Clercq E Chem Pharm Bull (Tokyo); 1993 Mar; 41(3):516-21. PubMed ID: 8386594 [TBL] [Abstract][Full Text] [Related]
15. Potent and selective activity of a new carbocyclic nucleoside analog (carbovir: NSC 614846) against human immunodeficiency virus in vitro. Vince R; Hua M; Brownell J; Daluge S; Lee FC; Shannon WM; Lavelle GC; Qualls J; Weislow OS; Kiser R Biochem Biophys Res Commun; 1988 Oct; 156(2):1046-53. PubMed ID: 2847711 [TBL] [Abstract][Full Text] [Related]
16. Synthesis of novel (2R,4R)- and (2S,4S)-iso dideoxynucleosides with exocyclic methylene as potential antiviral agents. Yoo SJ; Kim HO; Lim Y; Kim J; Jeong LS Bioorg Med Chem; 2002 Jan; 10(1):215-26. PubMed ID: 11738624 [TBL] [Abstract][Full Text] [Related]
17. Resolution of racemic carbovir and selective inhibition of human immunodeficiency virus by the (-) enantiomer. Vince R; Brownell J Biochem Biophys Res Commun; 1990 May; 168(3):912-6. PubMed ID: 2346492 [TBL] [Abstract][Full Text] [Related]
18. Cyclobut-A and cyclobut-G, carbocyclic oxetanocin analogs that inhibit the replication of human immunodeficiency virus in T cells and monocytes and macrophages in vitro. Hayashi S; Norbeck DW; Rosenbrook W; Fine RL; Matsukura M; Plattner JJ; Broder S; Mitsuya H Antimicrob Agents Chemother; 1990 Feb; 34(2):287-94. PubMed ID: 2327778 [TBL] [Abstract][Full Text] [Related]
19. The synthesis of branched-chain 3'-C-cyanomethyl-2',3'-dideoxy sugar nucleosides of adenine as potential inhibitors of the human immunodeficiency virus. Halmos T; Montserret R; Antonakis K Nucleic Acids Res; 1989 Oct; 17(19):7663-70. PubMed ID: 2798123 [TBL] [Abstract][Full Text] [Related]
20. Synthesis and antiviral evaluation of novel 6'(alpha)-methyl-branched Carbovir analogues. Kim JW; Hong JH Arch Pharm (Weinheim); 2005 Sep; 338(9):399-404. PubMed ID: 16143957 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]