Methods for processing chemical compounds having reactive...

Chemistry: molecular biology and microbiology – Measuring or testing process involving enzymes or... – Involving nucleic acid

Reexamination Certificate

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C435S091500, C435S091500, C540S472000, C540S473000, C540S474000

Reexamination Certificate

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06942966

ABSTRACT:
Novel macrocyclic compounds are constructed to include large cyclic structures that are interrupted by at least one ring system. Each interrupting ring system includes two bridgehead atoms. Bridgehead atoms are bonded to one or more bridges that interconnect one or more ring systems thereby forming a large cyclic structure. Located in each bridge are two or more nitrogenous moieties that are derivatized with chemical functional groups. The ring systems can include further nitrogenous moieties, either as ring atoms or on pendant groups attached to the ring. These can also be derivatized with chemical functional groups. The totality of the chemical functional groups imparts certain conformational and other properties to the macrocyclic compounds. In accordance with certain embodiments of the invention, libraries of such macrocyclic compounds are prepared utilizing permutations and combinations of the chemical functional groups and the nitrogenous moieties to build complexity into the library.

REFERENCES:
patent: 5142047 (1992-08-01), Summerton et al.
patent: 5225533 (1993-07-01), Rutter et al.
patent: 5264562 (1993-11-01), Matteucci
patent: 5276131 (1994-01-01), Akkapeddi et al.
patent: 5288514 (1994-02-01), Ellman
patent: 5324483 (1994-06-01), Cody et al.
patent: 5385893 (1995-01-01), Kiefer
patent: 5410045 (1995-04-01), Sessler et al.
patent: WO 91/19735 (1991-12-01), None
patent: WO 92/05186 (1992-04-01), None
patent: WO 92/20822 (1992-11-01), None
patent: WO 93/04204 (1993-03-01), None
patent: WO 94/08051 (1994-04-01), None
patent: WO 94/22454 (1994-10-01), None
patent: WO 94/24314 (1994-10-01), None
patent: WO 94/26775 (1994-11-01), None
patent: WO 94/27719 (1994-12-01), None
patent: WO 94/28028 (1994-12-01), None
patent: WO 94/28424 (1994-12-01), None
patent: WO 96/30377 (1996-10-01), None
Carey, F. A., “Advanced Organic Chemistry”, New York: Plenum Press, 1990, Third Edition, Part B, pp. 677-678.
PCT International Search Report dated Dec. 1, 1997, 2 pages.
Gallop, M.A. et al., “Applications of Combinatorial Technologies to Drug Discovery. 1. Background and Peptide Combinatorial Libraries”,J. Med. Chem., 1994, 37(9), 1233-1251.
Geysen, H. et al., “Srategies for Epitope Analysis Using Peptide Synthesis”,J. Immun. Meth. 1987, 102, 259-274.
Owens, R. et al.,“The Rapid Identification of HIV Protease Inhibitors Through the Synthesis and Screening of Defined Peptide Mixtures”,Biochem&Biophys. Res. Comm. 1991, 181, 402-408.
Wyatt, J. et al., “Combinatorially Selected Guanosine-Quartet Structure is a Potent Inhibitor of Human Immunodeficiency Virus Envelope-Mediated Cell Fusion”,Proc. Natl. Acad. Sci. USA1994, 91, 1356-1360.
Ecker, D. et al., “Rational Screening of Oligonucelotide Combinatorial LIbraries for Drug Discovery”,Nucleic Acides Res. 1993, 21, 1853-1856.
Simon, R. et al., “Peptides: A Modular Approach to Drug Discovery”,Proc. Natl. Acad. Sci. USA1992, 89, 9367-9371.
Zuckerman, R. et al., “Efficient Method for the Preparation of Peptoids [Oligo(N-substituted glycines)] by Submonomer Solid Phase Synthesis”,J. Amer. Chem. Soc. 1992, 114, 10646-10647.
Ohlmeyer, M. et al., “Complex Synthetic Chemical Libraries Indexed with Molecular Tags”,Proc. Natl. Acad. Sci. USA1993, 90, 10922-10926.
Vogtle, F., “Cyclophane Chemistry, Synthesis, Structures and Reactions”, John Wiley & Sons, New York, NY 1993.
Bradshaw, J. et al., “Aza-Crown Macrocycles”, John Wiley & Sons, New York, NY 1993.
Dietrich, B. et al., “Macrocyclic Chemistry”, VCH, New York, NY 1993.
Englisch, U. and Gauss, “Chemically Modified Oligonucelotides as Probes and Inhibitors”,Angew. Chem. Int. Ed. Engl. 1991, 30, 613-722.
Beaucage, S. and Iyer, “Advances in the Synthesis of Oligonuclelotides by the Phosphoramidite Approach”,Tetrahedron Letters1992, 48, 2223-2311.
Alul, R. et al., “Oxalyl-CPG: A Liable Support for Synthesis of Sensitive Oligonucleotide Derivatives”,Nucleic Acids Research1991, 19, 1527-1532.
Wright, P. et al., “Large Scale Synthesis of Oligonucleotides via Phoshoramidite Nucleosides and a High-loaded Polystyrene Support”,Tetrahedron Letters1993, 34, 3373-3376.
Hata, T. et al., “One-step Synthesis of 5′-Azido-nucleosides”,J. Chem. Soc. Perkin I1980, 306-310.
Dennis, E., “Phospholipases”,The Enzymes, 16, Chapter 9, pp. 307-353, Boyer, P.D., ed., Academic Press, New York, 1983.
Pruzanski, W. et al., “Enzymatic Activity and Immunoreactivity of Extracellular Phospholipase A2in Inflammatory Synovial Fluids”,Inflammation1992, 16, 451-457.
Vishwanath, B. et al., “Edema-Inducing Activity of Phospholipase A2Purified from Human Synovial Fluid and Inhibition by Aristolochic Acid”,Inflammation1988, 12, 549-561.
Bomalaski, J. et al., “Human Extracellular Recombinant Phospholipase A2Induces an Inflammatory response in Rebbit Joint”,J. of Immunology1991, 146, 3904-3910.
“Concise Encyclopedia of Polymer Science and Engineering”, 858-859, Kroschwitz, J.I., ed. John Wiley & Sons, 1990.
Green and Wuts,Protective Groups in Organic Synthesis, 2d edition, John Wiley & Sons, New York, 1991.
Saab, N.H. et al., “Synthesis and Evaluation of Unsymmetrically Substituted Polyamine Analogues as Modulators of Human Spermidine/Spermine-N1-Acetyltransferase (SSAT) and as Potential Antitumer Agents”,J. Med. Chem. 1993, 36, 2998-3004.
DeWitt, S.H. et al., “Diversomers”: An approach to Nonpeptide, Nonoligomeric Chemical Diversity,Proc. Natl. Acad. Sci. USA, 1993, 90, 6909-6913.
Carell, T. et al., “A Novel Procedure for the Syntehsis of Libraries Containing Small Organic Molecules”,Angew. Chem. Int. Ed. Engel., 1994, 33, 2061-2064.
Saari, W., et al., “Cyclization-Activated Prodrugs. Basic Carbamates of 4-Hydroxyanisole”,J. Med. Chem., 1990, 33, 94-101.
McMurry, et al., “Convenient Synthesis of Bifunctional Tetraaza Macrocycles,”Bioconjugate Chem., 1992, 3, 108-117.
Glaser, K., et al., “Phospholipase A2Enzymes: Regulation and Inhibition,”TiPs Reviews, 1992, 14, 92-98.
Mellor, D.P., Chemistry of Chelation and Chelating Agents in International Encyclopedia of Pharmacolaogy and Therapeutics, Section 70, The Chelation of Heavy Metals, Levine, W.G. Ed., Pergamon Press, Elmford, N.Y., 1979.
Hiroshige et al., “Palladium-mediated Macrocyclization on Solid Support and Its Applications to Combinatorial Synthesis,”J. Amer.Chem.Soc., Jul. 1995, vol. 117, pp. 11590-11591.
Kikuchi et al., “Molecular Recognition by Macrocyclic Receptors Having Miltiple Hydrophobic Branches in a Synthetic Bilayer Membrane,”J. Phys. Org. Chem., 1992, vol. 5, pp. 633-643.
Irie et al., “Method for Producing Carbamoyloxa-crosslinked Metacyclophane Compounds,” Chem. abstr., issued 1996, vol. 124, No. 7, (Columbus, Ohio, USA), p. 1319, col. 2, the abstract No. 87049y, JP 07-233,173 (Sep. 5, 1995), see entire abstract.
Sutherland, I.O., “Cyclophanes as Synthetic Receptors,”Pure and Applied Chem., 1990, vol. 62, No. 3, pp. 449-504.
Trofimenko, S., “1,1,2,2-Ethanetetracarboxaldehyde Its Reactions”,J. Org. Chem., 1964, 29, 3046.
Iwata et al., “Synthesis and Characterization of Macrocyclic Polyaza (2,5) pyridinophanes Possessing Vitamin B6Functionality”,Bull. Chem. Soc. Jpn., 1986, 10 59, 31-1036.
Vogtle et al., “Sterische Wechselwirkungen Im Innern Cyclischer Verbindungen, 14: Diaza-Und Dioxa-Phane”,Tetra. Lett., 1970, 2, 115-118.
Abdel-Magid, A et al., “Reduction Amination of Aldehydes and Ketones by Using Sodium Triacetoxyborohydride”,Tetra. Lett., 1990, 31(39), 5595-5598.
Augustyns, K. et al., “Influence of the Incorporation of (S)-9-(3,1-dihydroxy-butyl)adenine on the Enzymatic Stability and Base-Pairing Properties of Oligodeoxynucleotides”

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