Patent US4548926A successfully refreshed from Google Patents.
US4548926A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Hypotensive peptides and their use
Assignee: Sankyo Co Ltd
•
Filing: 1984-06-07
•
Granted: 1985-10-22
•
Expires: 2004-06-07
Abstract
Abstract Oligopeptides of formula (I) ##STR1## (wherein R 1 CO-- is an acyl group. But is an isobutyl or sec-butyl group and X is a variety of organic groups) and salts and esters thereof have valuable renin inhibitory activity.
Inventors
- 👤 Rei Matsueda
- 👤 Yuichiro Yabe
- 👤 Mitsuo Yamazaki
- 👤 Tatsuo Kokubu
- 👤 Kunio Hiwada
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-11-07 21:54
CPC Classifications
C; C07; C07D; C07D233/00; C07D233/54; C07D233/64; A; A61; A61P; A61P43/00; A61P9/00; A61P9/12; C07F; C07F7/00; C07F7/02; C07F7/08; C07F7/18; C07F7/1804; C07F9/00; C07F9/02; C07F9/28; C07F9/38; C07F9/3804; C07F9/3808; C07K; C07K5/00; C07K5/02; C07K5/0227; C07K5/04; C07K5/06; C07K5/06008; C07K5/06078; C07K5/06139; C07K5/06156; C07K5/06191; C07K5/08; C07K5/0802; C07K5/0812; A61K; A61K38/00; Y; Y10; Y10S; Y10S530/00; Y10S530/80; Y10S530/86
Claims Analysis
Total Claims: 20
Claim 1
Independent Claim
223 words
Compounds of formula (I): ##STR36## wherein: R 1 represents a C 1 -C 4 alkyl group having: (a) an amino or protected amino substituent on its α-carbon atom and (b) a phenyl or naphthyl group, a 5- or 6-membered heterocyclic group having one or more of hetero atoms selected from nitrogen, oxygen and sulfur atoms, a 3-indolinyl group or a 1,2,3,4-tetrahydro-β-carbolin-3-yl group, said R 1 C0-- having one or more substituents selected from an amino group and a protected amino group; or R 1 represents a 1,2,3,4-tetrahydro-β-carbolin-3-yl group or a 1,2,3,4-tetrahydro-β-carbolin-1-yl group; But represents a butyl group selected from the isobutyl and sec-butyl groups; X represents the formyl group or, a group of formula --CH(R 2 )--Y wherein R 2 is a hydrogen atom, an alkyl group of 1 to 8 carbon atoms or a substituted alkyl group of 1 to 8 carbon atoms and having at least one substituent selected from a hydroxy, mercapto, amino, carbamoyl, formyl, phenyl, naphthyl or 5- or 6-membered heterocyclic group having one or more of hetero atoms of N, O and S, and Y is hydroxy, mercapto or formyl; and the carbon atoms marked with (S) are of the S-configuration; provided that R 1 does not represent the benzyloxycarbonyl-L-phenylalanyl group or the benzyloxycarbonyl-L-prolyl-L-phenylalanyl group when X represents the formyl group; and pharmaceutically acceptable salts and esters thereof.
Claim 2
Dependent Claim
223 words
Compounds of formula (I): ##STR36## wherein: R 1 represents a C 1 -C 4 alkyl group having: (a) an amino or protected amino substituent on its α-carbon atom and (b) a phenyl or naphthyl group, a 5- or 6-membered heterocyclic group having one or more of hetero atoms selected from nitrogen, oxygen and sulfur atoms, a 3-indolinyl group or a 1,2,3,4-tetrahydro-β-carbolin-3-yl group, said R 1 C0-- having one or more substituents selected from an amino group and a protected amino group; or R 1 represents a 1,2,3,4-tetrahydro-β-carbolin-3-yl group or a 1,2,3,4-tetrahydro-β-carbolin-1-yl group; But represents a butyl group selected from the isobutyl and sec-butyl groups; X represents the formyl group or, a group of formula --CH(R 2 )--Y wherein R 2 is a hydrogen atom, an alkyl group of 1 to 8 carbon atoms or a substituted alkyl group of 1 to 8 carbon atoms and having at least one substituent selected from a hydroxy, mercapto, amino, carbamoyl, formyl, phenyl, naphthyl or 5- or 6-membered heterocyclic group having one or more of hetero atoms of N, O and S, and Y is hydroxy, mercapto or formyl; and the carbon atoms marked with (S) are of the S-configuration; provided that R 1 does not represent the benzyloxycarbonyl-L-phenylalanyl group or the benzyloxycarbonyl-L-prolyl-L-phenylalanyl group when X represents the formyl group; and pharmaceutically acceptable salts and esters thereof.
Claim 3
Dependent Claim
25 words
Compounds as claimed in claim 1, having the formula (Ia): ##STR37## (in which R 1 , X and S are as defined in claim 1).
Claim 4
Dependent Claim
25 words
Compounds as claimed in claim 1, having the formula (Ib): ##STR38## (in which R 1 , X and S are as defined in claim 1).
Claim 5
Dependent Claim
58 words
Compounds as claimed in any one of claims 2, 3 or 1, wherein the acyl group represented by R 1 CO-- is selected from the phenylalanyl, N-(benzyloxycarbonyl)phenylalanyl, alpha-(benzyloxycarbonylamino)phenylacetyl, N-(4-phenylbutyryl)phenylalanyl, 2-hydroxy-3-phenylpropionyl, N-(benzyloxycarbonyl)tyrosyl, N-(2-nitrophenylthio)phenylalanyl, N-(3-nitro-2-pyridylthio)phenylalanyl, 2-benzyloxycarbonylamino-3-(1-naphthoyl)propionyl, 2-benzyloxycarbonylamino-3-(2-naphthoyl)propionyl, N-benzyloxycarbonyl-3-(3-quinolyl)-L-alanyl and N-benzyloxycarbonyl-3-(8-quinolyl)-L-alanyl groups, and groups having the formulae: ##STR39## in which Boc represents the t-butoxycarbonyl group and Z represents the benzyloxycarbonyl group.
Claim 6
Dependent Claim
45 words
Compounds as claimed in any one of claims 2, 3 or 1, wherein the group represented by X is selected from the formyl, hydroxymethyl, formylmethyl, 2-formyl-1-hydroxyethyl, 1,2-dihydroxyethyl, 1,3-dihydroxypropyl, 2-hydroxy-1-mercaptoethyl groups and groups of formulae ##STR40## in which n represents an integer from 2 to 8.
Claim 7
Dependent Claim
25 words
Compounds as claimed in claim 1, selected from the group consisting of: N-(4-phenylbutyryl)-L-phenylalanyl-L-histidyl-L-leucinal, N-[3-(3-nitro-2-pyridyldithio)propionyl]-L-phenylalanyl-L-histidyl-L-leucinal, N-benzyloxycarbonyl-3-(1-naphthyl)-L-alanyl-L-histidyl-L-leucinal, N-benzyloxycarbonyl-L-phenylalanyl-L-histidyl-L-leucinol, N-[3-(3-nitro-2-pyridyldithio)propionyl]-L-phenylalanyl-L-histidyl-L-leucinol, N-benzyloxycarbonyl-3-(1-naphthyl)-L-alanyl-L-histidyl-L-leucinol, and pharmaceutically acceptable salts and esters thereof.
Claim 8
Dependent Claim
7 words
N-(4-phenylbutyryl)-L-phenylalanyl-L-histidyl-L-leucinal of the formula of claim 1.
Claim 9
Dependent Claim
7 words
N-[3-(3-nitro-2-pyridyldithio)propionyl]-L-phenylalanyl-L-histidyl-L-leucinal of the formula of claim 1.
Claim 10
Dependent Claim
7 words
N-benzyloxycarbonyl-3-(1-naphthyl)-L-alanyl-L-histidyl-L-leucinal of the formula of claim 1.
Claim 11
Dependent Claim
7 words
N-benzyloxycarbonyl-L-phenylalanyl-L-histidyl-L-leucinol of the formula of claim 1.
Claim 12
Dependent Claim
7 words
N-[3-(3-nitro-2-pyridyldithio)propionyl]-L-phenylalanyl-L-histidyl-L-leucinol of the formula of claim 1.
Claim 13
Dependent Claim
7 words
N-benzyloxycarbonyl-3-(1-naphthyl)-L-alanyl-L-histidyl-L-leucinol of the formula of claim 1.
Claim 14
Independent Claim
255 words
A method of treating angiotensin-induced hypertension in a mammal, by administering to said mammal an effective amount of a renin inhibitor, wherein said renin inhibitor is selected from the group consisting of compounds of formula (I): ##STR41## wherein: R 1 represents a C 1 -C 4 alkyl group having: (a) an amino or protected amino substituent on its α-carbon atom and (b) a phenyl or naphthyl group, a 5- or 6-membered heterocyclic group having one or more of hetero atoms selected from nitrogen, oxygen and sulfur atoms, a 3-indolinyl group or a 1,2,3,4-tetrahydro-β-carbolin-3-yl group, said R 1 CO-- having one or more substituents selected from an amino group and a protected amino group; or R 1 represents a 1,2,3,4-tetrahydro-β-carbolin-3-yl group or a 1,2,3,4-tetrahydro-β-carbolin-1-yl group; But represents a butyl group selected from the isobutyl and sec-butyl groups; X represents the formyl group or, a group of formula --CH(R 2 )--Y wherein R 2 is a hydrogen atom, an alkyl group of 1 to 8 carbon atoms or a substituted alkyl group of 1 to 8 carbon atoms and having at least one substituent selected from a hydroxy, mercapto, amino, carbamoyl, formyl, phenyl, naphthyl or 5- or 6-membered heterocyclic group having one or more of hetero atoms of N, O and S, and Y is hydroxy, mercapto or formyl; and the carbon atoms marked with (S) are of the S-configuration; provided that R 1 does not represent the benzyloxycarbonyl-L-phenylalanyl group or the benzyloxycarbonyl-L-prolyl-L-phenylalanyl group when X represents the formyl group; and pharmaceutically acceptable salts and esters thereof.
Claim 15
Independent Claim
255 words
A method of treating angiotensin-induced hypertension in a mammal, by administering to said mammal an effective amount of a renin inhibitor, wherein said renin inhibitor is selected from the group consisting of compounds of formula (I): ##STR41## wherein: R 1 represents a C 1 -C 4 alkyl group having: (a) an amino or protected amino substituent on its α-carbon atom and (b) a phenyl or naphthyl group, a 5- or 6-membered heterocyclic group having one or more of hetero atoms selected from nitrogen, oxygen and sulfur atoms, a 3-indolinyl group or a 1,2,3,4-tetrahydro-β-carbolin-3-yl group, said R 1 CO-- having one or more substituents selected from an amino group and a protected amino group; or R 1 represents a 1,2,3,4-tetrahydro-β-carbolin-3-yl group or a 1,2,3,4-tetrahydro-β-carbolin-1-yl group; But represents a butyl group selected from the isobutyl and sec-butyl groups; X represents the formyl group or, a group of formula --CH(R 2 )--Y wherein R 2 is a hydrogen atom, an alkyl group of 1 to 8 carbon atoms or a substituted alkyl group of 1 to 8 carbon atoms and having at least one substituent selected from a hydroxy, mercapto, amino, carbamoyl, formyl, phenyl, naphthyl or 5- or 6-membered heterocyclic group having one or more of hetero atoms of N, O and S, and Y is hydroxy, mercapto or formyl; and the carbon atoms marked with (S) are of the S-configuration; provided that R 1 does not represent the benzyloxycarbonyl-L-phenylalanyl group or the benzyloxycarbonyl-L-prolyl-L-phenylalanyl group when X represents the formyl group; and pharmaceutically acceptable salts and esters thereof.
Claim 16
Dependent Claim
40 words
A method as claimed in claim 13, wherein said renin inhibitor is selected from compounds of formula (Ia): ##STR42## (in which R 1 , X and S are as defined in claim 13) and pharmaceutically acceptable salts and esters thereof.
Claim 17
Dependent Claim
40 words
A method as claimed in claim 13, wherein said renin inhibitor is selected from compounds of formula (Ib): ##STR43## (in which R 1 , X and S are as defined in claim 13) and pharmaceutically acceptable salts and esters thereof.
Claim 18
Independent Claim
71 words
A method as claimed in any one of claims 14, 15 or 13, wherein the acyl group represented by R 1 CO-- is selected from the acetyl, propionyl, pivaloyo, benzoyl, 2-methoxycarbonylbenzoyl, 1-naphthoyl, 2-naphthoyl, phenylacetyl, benzyloxycarbonyl, phenylalanyl, N-(benzyloxycarbonyl)phenylalanyl, alpha-(benzyloxycarbonylamino)phenylacetyl, N-(4-phenylbutyryl)phenylalanyl, 2-hydroxy-3-phenylpropionyl, N-(benzyloxycarbonyl)-tyrosyl, N-(2-nitrophenylthio)phenylalanyl, N-(3-nitro-2-pyridylthio)phenylalanyl, 2-benzyloxycarbonylamino-3-(1-naphthoyl)propionyl, 2-benzyloxycarbonylamino-3-(2-naphthoyl)propionyl, nicotinyl, 2-pyridinecarbonyl, N-benzyloxycarbonyl-3-(3-quinolyl)-L-alanyl and N-benzyloxycarbonyl-3-(8-quinolyl)-L-alanyl groups, and the groups having the formulae: ##STR44## in which Boc represents the t-butoxycarbonyl group and Z represents the benzyloxycarbonyl group.
Claim 19
Independent Claim
50 words
A method as claimed in any one of claims 14, 15 or 13, wherein the group represented by X is selected from the formyl, hydroxymethyl, formylmethyl, 2-formyl-1-hydroxyethyl, 1,2-dihydroxyethyl, 1,3-dihydroxypropyl, 2-hydroxy-1-mercaptoethyl, phosphono, hydroxo(2-hydroxyethyl)oxophosphorio and (formylmethyl)hydroxooxophosphorio groups and groups of formulae ##STR45## in which n represents an integer from 2 to 8.
Claim 20
Dependent Claim
27 words
A method as claimed in claim 13, wherein said renin inhibitor is selected from: N-(4-phenylbutyryl)-L-phenylalanyl-L-histidyl-L-leucinal, N-[3-(3-nitro-2-pyridyldithio)propionyl]-L-phenylalanyl-L-histidyl-L-leucinal, N-benzyloxycarbonyl-3-(1-naphthyl)-L-alanyl-L-histidyl-L-leucinal, N-benzyloxycarbonyl-L-phenylalanyl-l-histidyl-L-leucinol, N-[3-(3-nitro-2-pyridyldithio)propionyl]-L-phenylalanyl-L-histidyl-L-leucinol, N-benzyloxycarbonyl-3-(1-naphthyl)-L-alanyl-L-histidyl-L-leucinol, and pharmaceutically acceptable salts and esters thereof.
References Cited (Backward Citations)
No citation records indexed.
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1988-10-21 | 1989-04-22 | 1989-10-22 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1992-10-21 | 1993-04-22 | 1993-10-22 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1996-10-21 | 1997-04-22 | 1997-10-22 | $7700.00 | Window Closed / Lapsed |