Effectors of dipeptidyl peptidase IV for topical use

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai

Reexamination Certificate

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C514S183000, C424S094630, C424S078020, C544S141000, C548S200000, C548S400000, C548S535000

Reexamination Certificate

active

06949515

ABSTRACT:
The invention relates to compounds for topically influencing the activity of dipeptidyl peptidase of the general formulawhereinA is an amino acid having at least one functional group in the side chain;B is a chemical compound covalently bound to a functional group of the side chain of A, chosen from the group consisting of(a) oligopeptides having a chain length of up to 20 amino acids,(b) homopolymers of glycine consisting of up to 6 glycine monomers, and(c) polyethylene glycols having molar masses of up to 20 000 g/mol; andC is a group amide-bonded to A chosen from the group consisting of thiazolidine, pyrrolidine, cyanopyrrolidine, hydroxyproline, dehydroproline or piperidine.The invention further relates to the use of said compounds for targeted intervention in local immunological processes (chemotaxis, inflammatory processes, autoimmune diseases), as well as effective and targeted treatment of pathophysiological and physiological processes related thereto (psoriasis, periodontitis, arthritis, allergies, inflammation), inter alia.

REFERENCES:
patent: 2961377 (1960-11-01), Shapiro et al.
patent: 3174901 (1965-03-01), Sterne
patent: 3879541 (1975-04-01), Kabbe et al.
patent: 3960949 (1976-06-01), Ahrens et al.
patent: 4028402 (1977-06-01), Fischer et al.
patent: 4935493 (1990-06-01), Bachovchin et al.
patent: 5433955 (1995-07-01), Bredehorst et al.
patent: 5462928 (1995-10-01), Bachovchin et al.
patent: 5512549 (1996-04-01), Chen et al.
patent: 5543396 (1996-08-01), Powers et al.
patent: 5614379 (1997-03-01), MacKellar
patent: 5624894 (1997-04-01), Bodor
patent: 5705483 (1998-01-01), Galloway et al.
patent: 5827898 (1998-10-01), Khandwala et al.
patent: 5939560 (1999-08-01), Jenkins et al.
patent: 6006753 (1999-12-01), Efendic
patent: 6011155 (2000-01-01), Villhauer
patent: 6107317 (2000-08-01), Villhauer
patent: 6110949 (2000-08-01), Villhauer
patent: 6124305 (2000-09-01), Villhauer
patent: 6166063 (2000-12-01), Villhauer
patent: 6172081 (2001-01-01), Damon
patent: 6201132 (2001-03-01), Jenkins et al.
patent: 6303661 (2001-10-01), Demuth et al.
patent: 6319893 (2001-11-01), Demuth et al.
patent: 6500804 (2002-12-01), Demuth et al.
patent: 6517824 (2003-02-01), Kohn et al.
patent: 6548481 (2003-04-01), Demuth et al.
patent: 296 075 (1991-11-01), None
patent: 196 16 486 (1997-10-01), None
patent: 0 658 568 (1995-06-01), None
patent: 0 708 179 (1996-04-01), None
patent: 1 130 022 (2001-09-01), None
patent: 04-288098 (1992-10-01), None
patent: 4334357 (1992-11-01), None
patent: WO 91/11457 (1991-08-01), None
patent: WO 91/16339 (1991-10-01), None
patent: WO 91/17767 (1991-11-01), None
patent: WO 93/08259 (1993-04-01), None
patent: WO 95/11689 (1995-05-01), None
patent: WO 95/15309 (1995-06-01), None
patent: WO 95/29691 (1995-11-01), None
patent: WO 97/40832 (1997-11-01), None
patent: WO 97/45117 (1997-12-01), None
patent: WO 98/19998 (1998-05-01), None
patent: WO 98/22494 (1998-05-01), None
patent: WO 99/46272 (1999-09-01), None
patent: WO 99/61431 (1999-12-01), None
patent: WO 99/62914 (1999-12-01), None
patent: WO 00/01849 (2000-01-01), None
patent: WO 00/10549 (2000-03-01), None
patent: WO 00/53171 (2000-09-01), None
patent: WO 01/09169 (2001-02-01), None
patent: WO 01/32624 (2001-05-01), None
patent: WO 01/34594 (2001-05-01), None
patent: WO 01/62266 (2001-08-01), None
patent: WO 01/74299 (2001-10-01), None
patent: WO 01/89569 (2001-11-01), None
patent: WO 01/94310 (2001-12-01), None
patent: WO 01/97808 (2001-12-01), None
patent: WO 02/20825 (2002-03-01), None
Bergmeier, Stephen C.,Tetrahedron, Elsevier Science Ltd.,“The Synthesis of Vicinal Amino Alcohols”, vol. 56, No. 17, (2000), pp. 2561-2576.
Kawamoto et al.,Tetrahedron Asymmetry, Elsevier Science Ltd.,“Anantioselective Synthesis of β-Hydroxy Amines and Aziridines Using Asymmetric Transfer Hydrogenation of α-Amido Ketones”, vol. 11, No. 16 (2000), pp. 3257-3261.
Orskov, Cathrine et al., “Proglucagon Products in Plasma of Noninsulin-dependent Diabetics and Nondiabetic Controls in the Fasting State and after Oral Glucose and Intravenous Arginine”J. Clin. Invest.,vol. 87, 1991, pp. 415-423.
Reinhold, D. et al.,Journal of Neuroimmunology,“Inhibitors of Dipeptidyl Peptidase IV/CD26 Suppress Activation of Human MBP-Specific CD4+ T Cell Clones”, (1998) 87:203-209.
Sengupta, et al.,Tetrahedron Letters, Elsevier Science Ltd.“Amino Acid Derived Morpholine Amides for Nucleophilic α-Amino Acylation Reactions: A New Synthetic Route to Enantiopure α-Amino Ketones”, vol. 40, No. 21 (1999), pp. 4107-4110.
Stöckel-Maschek, A., et al.,Biochimica et Biophysica Acta,“Thioxo Amino Acid Pyrrolidides and Thiazolidides: new Inhibitors of Proline Specific Peptidases”, (2000) 1479: 15-31.
Stryer, Lubert,Biochemistry,“Amino Acid Degradation and the Urea Cycle” (1975) pp. 451-452.
Mentlein et al.,Eur. J. Biochem,Dipeptidyl-Peptidase IV Hydrolyses Gastric Inhibitory Polypeptide, Glucagon-Like Peptide-1(7,36)Amide, Peptide Histidine Methionine and is Responsible for Their Degradation in Human Serum. (1993), 214, pp. 829-835.
Campbell, I.W.New Antidiabetic Drugs,ed. C.J. Bailey & P.R. Flatt, Smith-Gordon, “Sulphonylureas and metformin: efficacy and inadequacy”. 3:33-51 (1990).
The Merck Index, 11thEdition,An Encyclopedia of Chemicals, Drugs,and Biologicals, 1989, p. 934.
The Merck Index, 12thEdition,An Encyclopedia of Chemicals, Drugs,and Biologicals, 1996, p. 1014.
Martindale The Extra Pharmacopoeia,30thEdition, London Pharmaceutical Press, 1993, p. 1619, p. 36.
Chemical Abstracts,vol. 115. No. 15, Oct. 14, 1991 Columbus, Ohio, US; abstract No. 149947q. Schoen Ekkehard et al: “Dipeptidyl peptidase IV in the immune system. Effects of specific enzyme inhibitors on activity of dipeptidyl peptidase IV and proliferation of human lymphocytes”.
Chemical Abstracts,vol. 126, No. 2, Jan. 13, 1997 Columbus, Ohio, US; abstract No. 16161j, Stoeckel A. et al: “Competitive inhibition of proline specific enzymes by amino acid thioxopyrrolidides and thiazolidides”.
Chemical Abstracts,vol. 118, No. 25, Jun. 21, 1993 Columbus, Ohio, US; abstract No. 255342k, Hosoda, et al, “Preparation of N-(heterocyclic Carbonyl) Amino Acids and Analogs and Prolyl Endopeptidase Inhibitors”, Nov. 1992.
Arai et al., “Synthesis of prolyl endopeptidase inhibitors and evaluation of their structure-activity relationships : in vitro inhibition of prolyl endopeptidase from Canine Brain”Chemical and Pharmaceutical Bulletin.,Bd. 41, No. 9, 1993, pp. 1583-1588.
J. Lin et al.: “Inhibition of depeptidyl peptidase IV by fluorolefin-containing n-peptidyl-O-hydroxylamine peptidomimetics”Proceedings of the National Academy of Sciences of USA,vol. 95, Nov. 1998, pp. 14020-14024.
Korom, S., et al “Inhibition of CD26/dipeptidyl peptidase IV activity in vivo prolongs cardiac allograft survival in rat recipients”,Transplantation,vol. 63, 1495-1500 (Nov. 10 (1997).
Tanka, S., et al., “Suppression of arthritis by the inhibitors of dipeptidyl peptidase IV”,Int. J. Immunopharmacol,vol. 19, No. 1 pp. 15-24, (1997).
Mentlein, R., et al., “Proteolytic processing of neuropeptide Y and peptide YY by dipeptidyl peptidase IV”.Regul. Pept.49, 133-144 (1993).
Wetzel, W., et al., “Effects of the CLIP fragment ACTH 20-24 on the duration of REM sleep episodes”.Neuropeptides,31, 41-45 (1997).
Amasheh, S., et al., “Electrophysiological analysis of the function of the mammalian renal peptide transporter expressed inXenopus Laevisoocytes”.J. Physiol.504, 169-174 (1997).
Durinx, C.; et al.; “Reference Values for Plasma Dipepidyl-Pepidase IV activity and their Association with Other Laboratory Parameters”.Clin Chem Lab Med 2001,Feb.; 39 (2) :155-9, 1 page.
Gossrau, R.; “Cytochemistry of Membrane Proteases”,Histochem J,Jul. 1985; 17 (7) :737-71, 1 page.
Hahn, T.; et al.; “Enzyme Histochemical Evidence for the Pr

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