Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives
Patent
1992-03-05
1994-10-25
Brown, Johnnie R.
Organic compounds -- part of the class 532-570 series
Organic compounds
Carbohydrates or derivatives
536 2534, 536 245, C07H 19207
Patent
active
053590511
ABSTRACT:
Compositions and methods for modulating the activity of RNA are disclosed. In accordance with preferred embodiments, antisense compositions are prepared comprising targeting and reactive portions. In preferred embodiments, the reactive portions comprise one or two imidazole functionalities conjugated to the targeting oligonucleotide via linkers with and without intervening intercalating moieties and act through phosphorodiester hydrolytic bond cleavage. Therapeutics, diagnostics and research methods are also disclosed. Synthetic nucleosides and nucleoside fragments are also provided which are useful for elaboration of oligonucleotides for such purposes.
REFERENCES:
patent: 4814438 (1989-03-01), Armour et al.
patent: 4816569 (1989-03-01), Miyoshi
Tramontano et al., "Chemical Reactivity at an Antibody Binding Site Elicited by Mechanistic Design of a Synthetic Antigen," Proc. Nat. Acad. Sci. USA, 83, 6736-6740 (1986).
Inouye, "Antisense RNA: Its Functions and Applications in Gene Regulation-A Review," Gene, 72, 25-34, (1988).
Van Der Krol et al., "Antisense Genes in Plants: An Overview," Gene, 72, 45-50 (1988).
Zuckerman et al., "A Hybrid Sequence-Selective Ribonuclease S," J. Am. Chem. Soc., 110, 6592-6594 (1988).
Helene et al., "Control of Gene Expression by Oligodeoxynucleotides Covalently Linked to Intercalating Agents and Nucleic Acid Cleaving Reagents," Ch. 7 in Oligodeoxynucleotides, Antisense Inhibitors of Gene Expression, J. S. Cohen ed., CRC Press, Boca Raton, Fla., 1989, pp. 137-172.
Thuong et al., "Oligodeoxynucleotides Covalently Linked to Intercalating and Reactive Substances: Synthesis, Characterization and Physicochemical Studies," Ch. 2 in Oligodeoxynucleotides. Antisense Inhibitors of Gene Expression, J. S. Cohen ed., CRC Press, Boca Raton, Fla., 1989, pp. 24-51.
Knorre et al., "Oligonucleotides Linked to Reactive Groups," Ch. 8 in Oligodeoxynucleotides. Antisense Inhibitors of Gene Expression, J. S. Cohen ed., CRC Press, Boca Raton, Fla., 1989, pp. 173-196.
Akabori et al., "Synthese von Imidazolderivaten aus .alpha.-Aminosauren. III. Synthese von Zwei Hoheren Homologen des Histamins," Bull. Chem. Soc. Japan, 11, 208-213 (1936).
Rothenberg et al., "Oligodeoxynucleotides as Anti-Sense Inhibitors of Gene Expression: Therapeutic Implications," J. Nat. Cancer Inst. USA, 81(20), 1539-1544 (1989).
Kochetkov et al., Organic Chemistry of Nucleic Acids, Part B, Plenum Press, New York, 1972, pp. 488-490.
Offensperger et al., "In vivo Inhibition of Duck Hepatitis B Virus Replication and Gene Expression by Phosphorothioate Modified Antisense Oligodeoxynucleotides," EMBO J., 12(3), 1257-1262 (1993).
Simons et al., "Antisense c-myb Oligonucleotides Inhibit Intimal Arterial Smooth Muscle Cell Accumulation in vivo," Nature, 359, 67-70 (1992).
Burch et al., "Oligonucleotides Antisense of the Interleukin 1 Receptor mRNA Block the Effects of Interleukin 1 in Cultured Murine and Human Fibroblasts and in Mice," J. Clinical Investigations, 88, 1190-1196 (1991).
Kitajima et al., "Ablation of Transplanted HTLV-I Tax-Transformed Tumors in Mice by Antisense Inhibition of NF-kB," Science, 258, 1792-1795 (1992).
Higgins et al., "Antisense Inhibition of the p65 Subunit of NF-kB Blocks Tumorigenicity and Causes Tumor Regression," Proc. Nat. Acad. Sci. USA, 90, 9901-9905 (1993).
Vlassov, "Inhibition of Tick-Borne Viral Encephalitis Expression Using Covalently Linked Oligonucleotide Analogs," Abstract from program entitled Oligodeoxynucleotides as Antisense Inhibitors of Gene Expression: Therapeutic Implications, Natl. Cancer Inst. & Natl. Inst. of Allergy Infectious Dis. publ., Jun. 18-21, 1989, Rockville, Md.
C. A. Stein & J. S. Cohen, Cancer Research, vol. 48, pp. 2659-2668 (1988).
J. Walder, Genes & Development, vol. 2, pp. 502-504 (1988).
C. J. Marcus-Sekura, Anal. Biochemistry, vol. 172, 289-295 (1988).
G. Zon, Journal of Protein Chemistry, vol. 6, pp. 131-145 (1987).
G. Zon, Pharmaceutical Research, vol. 5, pp. 539-549 (1988).
A. R. Van der Krol, J. N. Mol. & A. R. Stuitje, BioTechniques, vol. 6, pp. 958-973 (1988).
D. S. Loose-Mitchell, TIPS, vol. 9, pp. 45-47 (1988).
Cazenave, N. Loreau, N. T. Thuong, J. J. Toulme and C. Helene in Nucleic Acid Research, vol. 15, pp. 4717-4736, (1987).
J. F. Constant, P. Laugaa, B. P. Roques & J. Lhomme, in Biochemistry, vol. 27, pp. 3997-4003 (1988).
A. T. Yeung, B. K. Jones and C. T. Chu in Biochemistry, vol. 27, pp. 2304-3210 (1988).
R. B. Meyer in the Journal of American Chemical Society, vol., 111, pp. 8517-8519 (1989).
D. G. Knorre an V. V. Vlassov, Progress in Nucleic Acid Research and Molecular Biology, vol. 32, pp. 291-320 (1985).
T. L. Doan, L. Perrouault, M. Chassignol, N. T. Thuong, & C. Helene, in Nucleic Acids Research, vol. 15, pp. 8643-8659 (1987).
D. S. Sigman, in Accounts of Chemical Research, vol. 19, pp. 180-186 (1986).
G. B. Dreyer and P. B. Dervan, in Proceedings of the National Academy of Sciences, U.S.A., vol. 82, pp. 968-972 (1985).
M. Caruthers, Oligonucleotides. Antisense Inhibitors of Gene Expression., pp. 7-24, J. S. Cohen, ed. (CRC Press, Inc. Boca Raton, Fla., 1989).
Journal of American Chemical Society, vol. 112, pp. 1253-1255 (1990) or elemental sulfur, S. Beaucage et al., Tetrahedron Letters, vol. 22, pp. 1859-1862 (1981).
Spalholtz et al., J. Virol., 61, 2128-2137 (1987).
Bruice Thomas
Cook Phillip D.
Guinosso Charles J.
Brown Johnnie R.
Crane L. Eric
ISIS Pharmaceuticals
LandOfFree
Compounds useful in the synthesis of nucleic acids capable of cl does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Compounds useful in the synthesis of nucleic acids capable of cl, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Compounds useful in the synthesis of nucleic acids capable of cl will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-136397