U.S. patents available from 1976 to present.
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Heterocyclic peptide renin inhibitors

Patent 5164388 Issued on November 17, 1992. Estimated Expiration Date: Icon_subject April 18, 2011. 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

2501455

3121717

3796703

Novel derivatives of N-(3,4,5-trimethoxy cinnamoyl)piperazine and the process for preparing them
Patent #: 4029650
Issued on: 06/14/1977
Inventor: Raynaud ,   et al.

Hypotensive peptides and their use
Patent #: 4548926
Issued on: 10/22/1985
Inventor: Matsueda ,   et al.

Aniline derivatives and cardiotonic composition
Patent #: 4585774
Issued on: 04/29/1986
Inventor: Tominaga ,   et al.

Renin inhibiting compounds
Patent #: 4645759
Issued on: 02/24/1987
Inventor: Luly ,   et al.

Renin inhibiting compounds
Patent #: 4652551
Issued on: 03/24/1987
Inventor: Luly ,   et al.

N-(acyldipeptidyl)-aminoglycols
Patent #: 4657931
Issued on: 04/14/1987
Inventor: Baran ,   et al.

Modified phenylalanine peptidylaminodiols
Patent #: 4680284
Issued on: 07/14/1987
Inventor: Luly ,   et al.

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Inventors

Application

No. 678266 filed on 04/18/1991

US Classes:

514/235.8, Plural ring nitrogens in the additional hetero ring (e.g., imidazole, pyrazine, etc.)514/18, 3 or 4 peptide repeating units in known peptide chain514/217.05, Plural ring hetero atoms in the additional hetero ring514/230.8, Chalcogen bonded directly to ring carbon of 1,4-oxazine ring514/231.5, Additional hetero ring attached directly or indirectly to the morpholine ring by nonionic bonding514/254.02, The additional five-membered hetero ring also has chalcogen as a ring member514/315, Piperidines514/326, The additional ring is a hetero ring514/345, Chalcogen bonded directly to ring carbon of the six-membered hetero ring514/397, Additional hetero ring540/492, Plural nitrogens in the hetero ring544/121, Piperazine ring544/132, Five-membered hetero ring having two or more ring hetero atoms of which at least one is nitrogen544/295, Plural diazine rings544/357, Plural diazine rings544/360, Six-membered ring consisting of one nitrogen and five carbons (e.g., pyridine, etc.)544/369, 1,3-oxazole ring or 1,3-thiazole ring (including hydrogenated)544/370, 1,3-diazole ring (including hydrogenated)544/375, Polycyclo ring system having the additional hetero ring as one of the cyclos544/384, Chalcogen bonded directly to piperazine ring carbon544/385, Plural chalcogens bonded directly to piperazine ring carbons544/392, Phenyl or naphthyl bonded directly to ring nitrogen of the piperazine ring544/398Chalcogen attached indirectly to the piperazine ring by nonionic bonding

Examiners

Primary: Daus, Donald G.

Attorney, Agent or Firm

Foreign Patent References

  • 76222/87 AU. 02/13/1988
  • 0189203 EP. 07/13/1986
  • 0228192 EP. 07/13/1987
  • 0229667 EP. 07/13/1987
  • 0231919 EP. 08/13/1987
  • 0310070 EP. 04/13/1989
  • 0310071 EP. 04/13/1989
  • 0310072 EP. 04/13/1989
  • 0310073 EP. 04/13/1989
  • 0311012 EP. 04/13/1989
  • 3721855 DE. 09/13/1988
  • WO87/02581 WO. 05/13/1987
  • WO87/02986 WO. 05/13/1987
  • WO87/05302 WO. 09/13/1987
  • WO88/02374 WO. 04/13/1988
  • WO88/05050 WO. 07/13/1988

International Class

A61K 031/495

Abstract

A renin inhibiting compound of the formula ##STR1## wherein X is N, O or CH; R1 is absent or a functional group; A and L are independently selected from absent, C=O, SO2 and CH2 ; D is C=O, SO2 or CH2 ; Y is N or CH; R2 is hydrogen, loweralkyl or substituted alkyl; Z is a functional group; R3 is loweralkyl or substituted alkyl; n is 0 or 1; and T is a mimic of the Leu-Val cleavage site of angiotensinogen; or a pharmaceutically acceptable salt, ester or prodrug thereof.

Other References

  • Chem. Abstr. vol. 108, Entry 38432d (1988) Abstract Ger. 3,601,248 (Breipohl)
  • Hansen, Biochem. Biophys. Res. Commun. 132 155 (1985)
  • Moore, Biochem. Biophys. Res. Commun., 159 420 (1989)
  • Billich, J. Biol. Chem., 263 1790S (1988)
  • Richards, FEBS Lett., 247 113 (1989
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