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Renin inhibitors, treatments and dipeptide synthesis

Assignee: Ferring AB
•
Filing: 1984-11-13
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Granted: 1986-09-02
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Expires: 2004-11-13
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Abstract

Abstract Preparation of renin inhibitors based on the structure of natural renin substrate at residues 6 to 13 from the amino terminal thereof, the inhibitors being polypeptide analogues having in particular an isosteric non-peptide link corresponding to the 10, 11 peptide link of the substrate, and preparation of dipeptide analogues.

Inventors

  • 👤 Michael Szelke
  • 👤 David M. Jones
  • 👤 Allan Hallett

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-09 10:58
CPC Classifications
C; C07; C07K; C07K5/00; C07K5/04; C07K5/08; C07K5/0819; A; A61; A61K; A61K38/00; Y; Y10; Y10S; Y10S530/00; Y10S530/86

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 287 words
A polypeptide analogue of the formula: ##STR64## or the partial sequences: X--A--B--Z--W (V)(i) X--His--A--B--Z--W (V)(ii) X--Phe--His--A--B--Z--W (V)(iii) X-Pro-Phe-His-A-B-Z-W (V)(iv) where: Pro, Phe and His are in substituted form; Pro by OH, Phe by OH, F, Cl, Br or Me, His by Me; or Phe is replaced by pGlu, Phe by Tyr or His by spinacin. X=H; or an N-protecting group; Y=D- or L-His or is absent; A= ##STR65## where the configuration at asymmetric centres * is either R or S, where in VIII the hydroxy group and protected in ether --OR 4 or ester ##STR66## form where R 4 is as given under W below and where R 1 and R 2 , the same or different= i Pro (isopropyl), i Bu (isobutyl) or Bzl (benzyl); R 3 =H or an N-protecting group; B=D- or L-Val Leu or Ile; Z=D- or L-Tyr, Phe, or His; and W=(i)--OH and in protected ester form as --OR 4 where R 4 =lower alkyl C 1 -C 5 ; or (ii)--NH 2 and in protected amide form as --NHR 5 or --N(R 5 ) 2 , wherein R 5 =an N-protecting group; or (iii) an L- or D-serine or L- or D-lysine or arginine and in amide form, or (iv) an amino alcohol residue derived therefrom as such or protected in ester or ether form or Z+W=an alcohol derived from L- or D-Tyr, Phe or His residue and protected in ester or ether form; isosteric links as set out above for A being in free form or in protected form at one or more nitrogen, carboxyl, hydroxy or other reactive groups or in salt form at amino imidazole or carboxyl groups as their physiologically acceptable acid addition salts at basic centres.
Claim 2
Dependent Claim 287 words
A polypeptide analogue of the formula: ##STR64## or the partial sequences: X--A--B--Z--W (V)(i) X--His--A--B--Z--W (V)(ii) X--Phe--His--A--B--Z--W (V)(iii) X-Pro-Phe-His-A-B-Z-W (V)(iv) where: Pro, Phe and His are in substituted form; Pro by OH, Phe by OH, F, Cl, Br or Me, His by Me; or Phe is replaced by pGlu, Phe by Tyr or His by spinacin. X=H; or an N-protecting group; Y=D- or L-His or is absent; A= ##STR65## where the configuration at asymmetric centres * is either R or S, where in VIII the hydroxy group and protected in ether --OR 4 or ester ##STR66## form where R 4 is as given under W below and where R 1 and R 2 , the same or different= i Pro (isopropyl), i Bu (isobutyl) or Bzl (benzyl); R 3 =H or an N-protecting group; B=D- or L-Val Leu or Ile; Z=D- or L-Tyr, Phe, or His; and W=(i)--OH and in protected ester form as --OR 4 where R 4 =lower alkyl C 1 -C 5 ; or (ii)--NH 2 and in protected amide form as --NHR 5 or --N(R 5 ) 2 , wherein R 5 =an N-protecting group; or (iii) an L- or D-serine or L- or D-lysine or arginine and in amide form, or (iv) an amino alcohol residue derived therefrom as such or protected in ester or ether form or Z+W=an alcohol derived from L- or D-Tyr, Phe or His residue and protected in ester or ether form; isosteric links as set out above for A being in free form or in protected form at one or more nitrogen, carboxyl, hydroxy or other reactive groups or in salt form at amino imidazole or carboxyl groups as their physiologically acceptable acid addition salts at basic centres.
Claim 3
Dependent Claim 79 words
A polypeptide analogue, according to claim 1, of the formula: ##STR67## where X, Y, Pro, Phe and His are as in claim 1 A is as in claim 1 except that R 1 and R 2 , the same or different= i Bu (isobutyl) or Bzl (benzyl) R 3 =--H; or --SO 2 Ph, --SO 2 C 6 H 4 CH 3 (p), Boc or formyl Z=Tyr, Phe; W=is as in claim 1 Z+W is as in claim 1.
Claim 4
Dependent Claim 92 words
A polypeptide analogue, according to claim 1 of the formula: ##STR68## where X, Y, Pro, Phe and His are as in claim 1 A is as in claim 1 except that R 1 = i Bu (isobutyl) or Bzl (benzyl) or other lipophilic or aromatic amino-acid side chain R 2 = i Pr (isopropyl), and R 3 =--H; or --SO 2 Ph, --SO 2 C 6 H 4 CH 3 (p), Boc or formyl: Z is as in claim 1 W is as in claim 2 Z+W is as in claim 1.
Claim 5
Dependent Claim 19 words
A polypeptide according to claim 1 modified by isosteric replacement, as set out therein, at Pro-Phe or Phe-His links.
Claim 6
Dependent Claim 18 words
A polypeptide according to claim 1 wherein the isosteric replacement at 10,11 position is of the "reduced" kind.
Claim 7
Dependent Claim 18 words
A polypeptide according to claim 1 wherein the isosteric replacement at 10,11 position is of the "hydroxy" kind.
Claim 8
Dependent Claim 21 words
A composition for treating heart failure comprising an effective amount of a polypeptide of claim 1 in a pharmaceutically acceptable carrier.

References Cited (Backward Citations)

US4424207A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-09-01 1990-03-03 1990-09-02 $2000.00 Window Closed / Lapsed
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