Potassium channel inhibitors

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Heterocyclic carbon compounds containing a hetero ring...

Reexamination Certificate

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C514S299000, C514S310000, C514S313000, C514S243000, C514S249000, C514S260100, C514S258100, C514S357000, C514S400000, C514S256000, C514S365000, C514S397000, C514S602000, C546S143000, C546S159000, C546S160000, C546S112000, C546S337000, C544S235000, C544S253000, C544S356000, C544S349000, C544S183000, C544S335000, C548S338100, C548S204000, C548S315100, C564S084000

Reexamination Certificate

active

06858611

ABSTRACT:
Compounds which are useful as potassium channel inhibitors and which because of their slow off-rates are especially useful for the treatment of cardiac arrhythmias are described.

REFERENCES:
patent: 3953506 (1976-04-01), Spicer et al.
patent: 4005140 (1977-01-01), Spicer et al.
patent: 4975453 (1990-12-01), Becker et al.
patent: 5006512 (1991-04-01), Ohnishi
patent: 5215985 (1993-06-01), Murphy et al.
patent: 5234947 (1993-08-01), Cherksey
patent: 5242947 (1993-09-01), Cherksey et al.
patent: 5310932 (1994-05-01), Atwal et al.
patent: 5328830 (1994-07-01), Janis et al.
patent: 5356775 (1994-10-01), Hebert et al.
patent: 5401758 (1995-03-01), Atwal et al.
patent: 5401848 (1995-03-01), Atwal
patent: 5451580 (1995-09-01), Murphy et al.
patent: 5453421 (1995-09-01), Atwal et al.
patent: 5486515 (1996-01-01), Brown et al.
patent: 6083986 (2000-07-01), Castle et al.
patent: 6333337 (2001-12-01), Gross et al.
patent: 6458794 (2002-10-01), Gross et al.
patent: 0 286 278 (1988-10-01), None
patent: 0 317 321 (1989-05-01), None
patent: 0 321 175 (1989-08-01), None
patent: 0 472 053 (1992-02-01), None
patent: 0 488 616 (1992-06-01), None
patent: 0 587 180 (1994-03-01), None
patent: 0 608 858 (1994-08-01), None
patent: 9518617 (1995-07-01), None
patent: 9526342 (1995-10-01), None
patent: 9621640 (1996-07-01), None
patent: 9636596 (1996-11-01), None
patent: 9725982 (1997-07-01), None
patent: 9725983 (1997-07-01), None
patent: 9726300 (1997-07-01), None
patent: 9804521 (1998-02-01), None
patent: 9836749 (1998-08-01), None
patent: 9937607 (1999-07-01), None
Lumma et al. (1987) J. Med. Chem. 30(5): 755-758).*
Still et al, “Rapid Chromatographic Technique for Preparative Separation with Moderate Resolution,” J. Org. Chem., vol. 43, No. 14, 1978, pp. 2923-2925.
Castle et al., “Characterization of 4-Aminopyridne Block of the Transient Outward K+Current in Adult Rat Ventricular Myocytes,” The Journal of Pharmacology and Experimental, vol. 264, No. 3, pp. 1450-1459.
Deal et al, “Molecular Physiology of Cardiac Potassium Channels,” Physiological Reviews, vol. 76, No. 1, Jan. 1996, pp. 49-67.
Wang et al, “Sustained Depolarization-Induced Outward Current in Human Atrial Myocytes, Evidence for a Novel Delayed Rectified K+Current Similar to Kvl.5 Cloned Channel Current,” Circulation Research, vol. 73, No. 6, Dec. 1993, pp. 1061-1076.
Hamill, “Improved Patch-Clamp Techniques for High-Resolution Current Recording from Cells and Cell-Free Membrane Patches,” Pflüger Archiv, (1981) 391:85-100.
Fedida et al, “Identity of a Novel Delayed Rectifier Current From Human Heart With a Cloned K+Channel Current,” Circulation Research, vol. 73, No. 1, Jul. 1993, pp. 210-216.
Chandy et al., “Voltage-Gated Potassium Channels are Required for Human T Lymphocyte Activation,” J. Exp. Med., vol. 160, Aug. 1984, pp. 369-385.
Sanguinetti, “Modulation of Potassium Channels by Antiarrhythmic and Antihypertensive Drugs,” Hypertension, vol. 19, No. E, Mar. 1992, pp. 228-236.
Lynch et al, “Therapeutic Potential of modulating Potassium, Currents in the Diseased Myocardium,” The FASEB Journal, vol. 6, Aug. 1992, p. 2952-2960.
Colatsky et al, “Channel Specificity in Antiarrhythmic Drug Action,” Circulation, vol. 82, No. 6, Dec. 1990, pp. 2235-2242.
Halliwell, “K+Channels in the Central Nervous System,” pp. 348-381.
Amos et al, “Differences Between Outward Currents of Human Atrial and Subepicardial Ventricular Myocytes,” Journal of Physiology, 1986, 491.1, pp. 31-50.
Wang et al, “Effects of Flecanide, Quinidine, and 4-Aminopyridine on Transient Outward and Ultrarapid Delayed Rectifier Currents in Human Atrial Myocytes,” The Journal of Pharmacology and Experimental Therapeutics, vol. 272, No. 1, pp. 184-196.
Lin et al. “Voltage-gated Potassium Channel Regulate Calcium-dependent Pathways Involved in Human T Lymphocyte Activation,” J. Exp. Med., vol. 177, pp. 637-645.
Kaczorowki et al, “lymphocyte Ion Channels as a Target for Immunosuppression,” Perspective in Drug Discovery and Design 2, 1994, pp. 233-248.
Leonard et al, “Selective Blockers of voltage-Gated K+Channels Depolarize Human T Lymphocytes: Mechanism of the Antiproliferative Effect of Charybdotoxin”, vol. 89, Nov. 1992, pp. 10094-10098.
Doupnik et al, “The Inward Rectifier Potassium Channel Family”, Current Opinion in Neurobiology, 1995, 5:268-277.
Chandy et al, “Voltage-Gated Potassium Channel Genes”, Handbook of Receptors and Channels, 1995, pp. 1-71.
Epps et al., Chemistry and Physics of Lipids, 69, 1994, pp. 137-150.
Chem Abs., vol. 104, No. 9 Abs No. 68632 (Mar. 3, 1986).
International Search Report PCT/US97/12559.
International Search Report PCTUS01/23258.
Robertson et al. J. Med. Chem. vol. 33, No. 6, 1990.

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