Nucleic acid labeling compounds

Details Nucleic acid labeling compounds Nucleic acid labeling compounds

2010-09-28

2011-12-13

Ward, Paul V. (Department: 1624)

Chemistry: molecular biology and microbiology

Measuring or testing process involving enzymes or...

Involving nucleic acid

C544S106000, C544S242000

Reexamination Certificate

active

08076072

ABSTRACT:
Nucleic acid labeling compounds including the following are disclosed:These compounds are useful for attaching a detectable label to a nucleic acid.

REFERENCES:
patent: 3352849 (1967-11-01), Shen
patent: 3817837 (1974-06-01), Rubenstein et al.
patent: 3850752 (1974-11-01), Schuurs et al.
patent: 3891623 (1975-06-01), Vorbruggen et al.
patent: 3939350 (1976-02-01), Kronick et al.
patent: 3996345 (1976-12-01), Ullman et al.
patent: 4275149 (1981-06-01), Litman et al.
patent: 4277437 (1981-07-01), Maggio
patent: 4366241 (1982-12-01), Tom et al.
patent: 4594339 (1986-06-01), Lopez et al.
patent: 4981783 (1991-01-01), Augenlicht
patent: 4997928 (1991-03-01), Hobbs, Jr.
patent: 5002867 (1991-03-01), Macevicz
patent: 5143854 (1992-09-01), Pirrung et al.
patent: 5151507 (1992-09-01), Hobbs, Jr. et al.
patent: 5202231 (1993-04-01), Drmanac et al.
patent: 5242796 (1993-09-01), Prober et al.
patent: 5262536 (1993-11-01), Hobbs, Jr.
patent: 5324633 (1994-06-01), Fodor et al.
patent: 5332666 (1994-07-01), Prober et al.
patent: 5422241 (1995-06-01), Goldrick et al.
patent: 5424186 (1995-06-01), Fodor et al.
patent: 5445934 (1995-08-01), Fodor et al.
patent: 5543292 (1996-08-01), Imai et al.
patent: 5571639 (1996-11-01), Hubbell et al.
patent: 5608063 (1997-03-01), Hobbs, Jr. et al.
patent: 5744305 (1998-04-01), Fodor et al.
patent: 6174998 (2001-01-01), Muhlegger et al.
patent: 6211158 (2001-04-01), Seela et al.
patent: 6864059 (2005-03-01), McGall et al.
patent: 7468243 (2008-12-01), McGall et al.
patent: 19509038 (1996-09-01), None
patent: 132621 (1985-02-01), None
patent: 159719 (1985-10-01), None
patent: 252683 (1988-01-01), None
patent: 266787 (1988-05-01), None
patent: 320308 (1989-06-01), None
patent: 322311 (1989-06-01), None
patent: 336731 (1989-10-01), None
patent: 535242 (1993-04-01), None
patent: 717113 (1996-06-01), None
patent: 721016 (1996-07-01), None
patent: 2551442 (1985-03-01), None
patent: 61 109797 (1986-05-01), None
patent: WO 89/10977 (1989-11-01), None
patent: WO 90/00626 (1990-01-01), None
patent: WO 90/03370 (1990-04-01), None
patent: WO 90/04652 (1990-05-01), None
patent: WO 90/15070 (1990-12-01), None
patent: WO 92/02258 (1992-02-01), None
patent: WO 92/10092 (1992-06-01), None
patent: WO 92/10588 (1992-06-01), None
patent: WO 93/16094 (1993-08-01), None
patent: WO 93/17126 (1993-09-01), None
patent: WO 95/00530 (1995-01-01), None
patent: WO 95/04594 (1995-02-01), None
patent: WO 95/04833 (1995-02-01), None
patent: WO 95/04834 (1995-02-01), None
patent: WO 95/11995 (1995-05-01), None
patent: WO 95/20681 (1995-08-01), None
patent: WO 95/30774 (1995-11-01), None
patent: WO 95/35505 (1995-12-01), None
patent: WO 96/28460 (1996-09-01), None
patent: WO 97/10365 (1997-03-01), None
patent: WO 97/27317 (1997-07-01), None
patent: WO 97/28176 (1997-08-01), None
patent: WO 97/29212 (1997-08-01), None
patent: WO 97/39120 (1997-10-01), None
patent: WO 98/11104 (1998-03-01), None
patent: WO 00/06771 (2000-02-01), None
Akita, Y. et al.,“Cross-Coupling Reaction of Chloropyrazines with Acetylenes,” Chemical & Pharmaceutical Bulletin, 34, 4 A.D., pp. 1447-1458.
Aoyagi, Mitsutoshi et al. “Nucleosides and nucleotides. 115. Synthesis of 3-alkyl-3-deazainosines via palladium-catalyzed intramolecular cyclization: A new conformational lock wi,” Tetrahedron Letters, 34, Jan. 1, 1993, pp. 103-106.
Avila, J. L. et al. “Biological action of pyrazolopyrimidine derivatives againstTrypanosoma cruzi. Studies in vitro and in vivo,” Comp Biochem.Physiol C., 86, 1987, pp. 49-54.
Barringer, K. J. et al. “Blunt-end and single-strand ligations byEscherichia coliligase: influence on an in vitro amplification scheme,” Gene, 89, Apr. 30, 1990, pp. 117-122.
Basnak, I. et al. “Some 6-aza-5-substituted-2′-deoxyuridines show potent and selective inhibition of herpes simplex virus type 1 thymidine kinase,” Nucleosides Nucleotides, 17, Jan. 1998, pp. 187-206.
Beabealashvilli, Robert S. et al. “Nucleoside 5′-triphosphates modified at sugar residues as substrates for calf thymus terminal deoxynucleotidyl transferase and for AMV reverse transcriptase,” Biochimica et Biophysica Acta (BBA)—Gene Structure and Expression, 868, Nov. 13, 1986, pp. 136-144.
Bergeron, et al.,“Reagents for the Stepwise Functionalization of Spermine,” J.Org.Chem., 53, 1998, pp. 3108-3111.
Bergstrom, D. E.,“Design and Synthesis of Heterocyclic Carboxamides as Natural Nucleic Acid Base Mimics,” Nucleosides Nucleotides, 15, 1996, pp. 59-68.
Bobek, M.,“Nucleic Acids Components and their Analogues. XCVII Synthesis of 5-Hydroxmethyl -6-Aza-2′-Deoxyuridine and 5-Hydroxymethyl-6-Aza-2′-Deoxycytidine,” Collection Czechoslov.Chem.Commun., 32, 2008, pp. 3581-3586.
Brody, R. S. et al. “The purification of orotidine-5′-phosphate decarboxylase from yeast by affinity chromatography,” J.Biol.Chem., 254, May 25, 1979, pp. 4238-4244.
Broude, N. E. et al. “Enhanced DNA sequencing by hybridization,” Proc.Natl.Acad.Sci.U.S.A, 91, Apr. 12, 1994, pp. 3072-3076.
Canard, B. et al. “Catalytic editing properties of DNA polymerases,” Proc.Natl.Acad.Sci.U.S.A, 92, Nov. 21, 1995, pp. 10859-10863.
Cech, D.,“New Approaches Toward the Synthesis of Non-Radioactively Labelled Nucleoside Triphosphates as Terminators for DNA Sequencing,” Collection Czechoslov.Chem.Commun., 61, 1996, pp. S297-S300.
Chee, M. et al. “Accessing genetic information with high-density DNA arrays,” Science, 274, Oct. 25, 1996, pp. 610-614.
Chernetskii, V. P.,“Anomalous Nucleosides and Related Compounds XIV. Derivatives of 6-Azacytidine,” Chemical Abstracts, 74, 1971.
Chidgeavadez, Z. G.,“2′, 3′-Dideoxy-3′ Amnionucleoside 5′-Triphosphates are the terminators of DNA Synthesis Catalyzed by DNA Polymerases,” Nucleic Acids Res., 12, 1984, pp. 1671-1686.
Chu,“General Synthesis of 2′, 3′-dideoxynucleosides and 2′,3′ didehydro-2′,3′-dideoxynucleosides,” J.Org.Chem., 54, 1989, pp. 2217-2225.
Cottam, H. B. et al. “New adenosine kinase inhibitors with oral antiinflammatory activity: synthesis and biological evaluation,” J.Med.Chem., 36, Oct. 29, 1993, pp. 3424-3430.
Curriden, M.,“A New Evidence Tool—First use of Mitochondrial DNA Test in a U.S. Criminal Trial,” ABA Journal, Nov. 1996, 1 pg.
Dansher, J. et al.,“Autometallographic Silver Amplification of Colloidal Gold,” J.Hisotech, 15, 1993, pp. 201-207.
Depelley, J. et al.,“New Non-Aromatic Triazinic Nucleosides: Synthesis and Antiretroviral Evaluation of Beta-Ribosylamine Nucleoside Analogs,” Nucleosides & Nucleotides, 15, 1996, pp. 995-1008.
Dueholm, et al. “2,3-dideoxy-furanoses in convergent synthesis of 2′, 3′-dideoxy nucleosides”, Synthesis, (1992), pp. 1-22.
Edo, K. et al.,“Studies on Pyrimidine Derivatives IX Coupling Reaction of Mono-Substituted Acetylenes with Iodopyrimidines,” Chemical & Pharmaceutical Bulletin, 26, 1978, pp. 3843-3850.
Eggers, M. et al. “A microchip for quantitative detection of molecules utilizing luminescent and radioisotope reporter groups,” Biotechniques, 17, Sep. 1994, pp. 516-525.
Feldman, W. et al. “Gray code masks for sequencing by hybridization,” Genomics, 23, Sep. 1, 1994, pp. 233-235.
Fodor, S. P. et al. “Light-directed, spatially addressable parallel chemical synthesis,” Science, 251, Feb. 15, 1991, pp. 767-773.
Freskos, J. N.,“Synthesis of 2′-Deoxypyrimidine Nucleosides Via Copper (I) Iodine Catalysis,” Nucleosides & Nucleotides, 8, 1989, pp. 549-555.
Galushko, S. V. et al. “Relationship between retention parameters in reversed-phase high-performance liquid chromatography and antitumour activity of some pyrimidine bases and nucleosides,” Journal of Chromatography A, 547, Jun.

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