U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Nitrosated and nitrosylated phosphodiesterase inhibitor compounds, compositions and their uses

Patent 6316457 Issued on November 13, 2001. Estimated Expiration Date: Icon_subject February 10, 2019. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Anorexigenic 4-[(3,4-dialkoxyphenyl)alkyl]-2-imidazolidinone derivatives
Patent #: 4308278
Issued on: 12/29/1981
Inventor: Schneider ,   et al.

Pyrimido-pyrimidine lipoxygenase inhibiting compounds
Patent #: 4963541
Issued on: 10/16/1990
Inventor: Brooks, et al.

Vaso-active medicament to treat impotence
Patent #: 5145852
Issued on: 09/08/1992
Inventor: Virag

Method for delivery of smooth muscle cell inhibitors
Patent #: 5171217
Issued on: 12/15/1992
Inventor: March, et al.

Medicaments for treating erectile disorders
Patent #: 5190967
Issued on: 03/02/1993
Inventor: Riley

Calcium independent C amp phosphodiesterase inhibitor antidepressant
Patent #: 5196426
Issued on: 03/23/1993
Inventor: Saccomano, et al.

Xanthine compounds and compositions, and methods of using them
Patent #: 5223504
Issued on: 06/29/1993
Inventor: Noverola, et al.

4-aryl-thiazole derivatives
Patent #: 5254575
Issued on: 10/19/1993
Inventor: Pick, et al.

5340827

S-nitrosothiols as smooth muscle relaxants and therapeutic uses thereof
Patent #: 5380758
Issued on: 01/10/1995
Inventor: Stamler, et al.

More ...

Inventors

Assignee

Application

No. 247323 filed on 02/10/1999

US Classes:

514/263.34, Chalcogen bonded directly to the 2-and 6- positions of the purine ring system (e.g., theophylline, etc.)544/272Nitrogen attached directly or indirectly to the purine ring system by nonionc bonding

Examiners

Primary: Shah, Mukund J.
Assistant: Rao, Deepak

Attorney, Agent or Firm

Foreign Patent References

  • 0252721 EP. 01/13/1988
  • 0 352 960 EP. 01/13/1990
  • 0442204 EP. 08/13/1991
  • 463756 EP. 01/13/1992
  • 0 463 756 EP. 01/13/1992
  • 0506194 EP. 09/13/1992
  • 2547501 FR. 12/13/1984
  • 9306103 WO. 04/13/1993
  • 9312068 WO. 06/13/1993
  • 9501338 WO. 01/13/1995
  • 9509636 WO. 04/13/1995
  • WO 95/26725 WO. 10/13/1995
  • 9526768 WO. 10/13/1995
  • WO 96 25184 WO. 08/13/1996
  • 9734871 WO. 09/13/1997
  • 9739760 WO. 10/13/1997
  • 9819672 WO. 05/13/1998

International Classes

C07D 487/04
A61K 031/418.8

Abstract

Disclosed are nitrosated and/or nitrosylated phosphodiesterase inhibitors having the formula NOn -PDE inhibitor where n is 1 or 2. The invention also provides compositions comprising such compounds in a pharmaceutically acceptable carrier. The invention also provides a composition comprising a therapeutically effective amount of an phosphodiesterase inhibitor (PDE inhibitor), which can optionally be substituted with at least one NO or NO2 moiety, and one to ten fold molar excess of a compound that donates, transfers or releases nitrogen monoxide as a charged species, i. e., nitrosonium (NO+) or nitroxyl (NO-), or as the neutral species, nitric oxide (NO⋅) or which stimulates endogenous EDRF production. The invention also provides compositions comprising such compounds in a pharmaceutically acceptable carrier. The invention also provides methods for treating sexual dysfunctions in males and females.

Other References

  • Takase et al., Chem. Abstract 119:203427, 1993.
  • Lugnier et al., Modulation of vascular cyclic nucleotide phosphodiesterases by cyclic GMP: role in vasodilation, Eur. Heart J., 14 Suppl. I, pp. 141-148 (PubMed Abstract), Nov. 1993.
  • Meskini et al., Phosphodiesterase inhibitory profile of some related xanthine derivatives pharmacologically active on the peripheral microcirculation, Biochem. Pharmacol., 47(5), pp. 781-788 (PubMed Abstract), Mar. 1994.
  • Zorgniotti et al, Int. J. Impotence Res., 6:33-36 (1994)
  • Boolell et al, Int. J. Impotence Res., 8:47-52 (1996)
  • Krane et al, New England Journal of Medicine, 321(24):1648-1659 (1989)
  • Trigo-Rocha et al, Neurourol. Urodyn., 13(1):71-80 (1994)
  • Sparwasser et al, J. Urol., 152:6, Pt. 1, pp. 2159-2163 (1994)
  • Chemical Abstracts, 120(1):612, Abstract 5451d (1994)
  • Chen et al, BJU International, 83:269-273 (1999)
  • Mathers et al, European Urology, 35(suppl 2):67 (abstract 266) (1999)
  • Park et al, Biochem. Biophys. Res. Commun., 249(3):612-617 (1998)
  • Terrett et al, Bioorg. Med. Chem. Lett., 6(15):1819-1824 (1996)
  • Boolell et al, British Journal of Urology, 78(2):257-261 (1996)
  • Martel et al, Drugs of the Future, 22(2) :138-143 (1997)
  • Chemical Abstracts, vol. 125, No. 15, Abstract No. 191382 (Oct. 7, 1996)
  • Chemical Abstracts, vol. 123, No. 1, Abstract No. 574 (Jul. 3, 1995)
  • Chemical Abstracts, vol. 120, No. 25, Abstract No. 315630 (Jun. 20, 1994)
  • Chemical Abstracts, vol. 121, No. 7, Abstract No. 73410 (Aug. 15, 1994)
  • Chemical Abstracts, vol. 116, No. 1, Abstract No. 4477 (Jan. 6, 1992)
  • Meskini, et al., Biochemical Pharm., vol. 47, No. 5, pp. 781-788, 1994
  • Lugnier, et al., European Heart Journal, 14 (Supp I): 141-148 (1993
PatentsPlus Images
Enhanced PDF formats
loading...
PatentsPlus: add to cart
PatentsPlus: add to cartSearch-enhanced full patent PDF image
$9.95more info
 
Sign InRegister
Username  
Password   
forgot password?