Method for treating renal disease
AssigneeAbbott Laboratories
InventorHollis D. Kleinert
Life of this patent
Estimating the term…
Abstract
The present invention relates to the use of renin inhibitors and to renin inhibitor compositions for prevention, treatment, inhibition or reversal of renal dysfunction or disease, especially renal failure.
Claims4
A method for treating or inhibiting renal dysfunction in a human comprising administering to said human a therapeutically effective amount of a compound of the formula:
- ##STR41## wherein A.sub.f is hydrogen, loweralkyl, arylalkyl, --OR.sub.10f or --SR.sub.10f wherein R.sub.10f is hydrogen, loweralkyl or aminoalkyl, --NR.sub.11f R.sub.12f wherein R.sub.11f and R.sub.12f are independently selected from hydrogen, loweralkyl, aminoalkyl, cyanoalkyl, hydroxyalkyl, carboxyalkyl, alkoxycarbonylalkyl, (amino)carboxyalkyl, ((N-protected)amino)carboxyalkyl, (alkylamino)carboxyalkyl, ((N-protected)alkylamino)carboxyalkyl, (dialkylamino)carboxyalkyl, (amino)alkoxycarbonylalkyl, ((N-protected)amino)alkoxycarbonylalkyl, (alkylamino)alkoxycarbonylalkyl, ((N-protected)alkylamino)alkoxycarbonylalkyl and (dialkylamino)alkoxycarbonylalkyl;
- or A.sub.f is ##STR42## wherein B.sub.f is NH, alkylamino, S, O, CH.sub.2 or CHOH and R23.sub.f is loweralkyl, cycloalkyl, aryl, arylalkyl, alkoxy, alkenyloxy, hydroxyalkoxy, dihydroxyalkoxy, arylalkoxy, arylalkoxyalkyl, amino, alkylamino, dialkylamino, (hydroxyalkyl)(alkyl)amino, (dihydroxyalkyl(alkyl)amino, aminoalkyl, N-protectedaminoalkyl, alkylaminoalkyl, (N-protected)(alkyl)aminoalkyl, dialkylaminoalkyl, carboxyalkoxyalkyl, (alkoxycarbonyl)alkoxyalkyl, carboxyalkyl, carboxyalkylamino, alkoxycarbonylalkyl, alkoxycarbonyalkylamino, (amino)carboxyalkyl, (amino)carboxyalkylamino, ((N-protected)amino)carboxyalkyl, ((N-protected)amino)carboxyalkylamino, (alkylamino)carboxyalkyl, (alkylamino)carboxyalkylamino, ((N-protected)alkylamino)carboxyalkyl, ((N-protected alkylamino)carboxyalkylamino, (dialkylamino)carboxyalkyl, (dialkylamino)carboxyalkylamino, (amino)alkoxycarbonylalkyl, (amino)alkoxycarbonylalkylamino, ((N-protected)amino)alkoxycarbonylalkyl, ((N-protected)amino)alkoxycarbonylalkylamino, (alkylamino)alkoxycarbonylalkyl, (alkylamino)alkoxycarbonylalkylamino, ((N-protected)alkylamino)alkoxycarbonylalkyl, ((N-protected)alkylamino)alkoxycarbonylalkylamino, (dialkylamino)alkoxycarbonylalkyl, (dialkylamino)alkoxycarbonylalkylamino, aminocycloalkyl, aminoalkylamino, dialkylaminoalkyl(alkyl)amino, arylalkylamino, arylalkyl(alkyl)amino, alkoxyalkyl(alkyl)amino,(polyalkyoxy)alkyl(alkyl)amino, di-(alkoxyalkyl)amino, di-(hydroxyalkyl)amino, di-((polyalkoxy)alkyl)amino, polyalkoxy, (polyalkoxy)alkyl, (heterocyclic)alkyl or a substituted or unsubstituted heterocyclic wherein saturated heterocyclics may be unsubstituted, monosubstituted or disubstituted with hydroxy, oxo amino, alkylamino, dialkylamino, alkoxy, polyalkoxy or loweralkyl;
- unsaturated hetercyclics may be unsubstituted or monosubstituted with hydroxy, amino, alkylamino, dialkylamino, alkoxy, polyalkoxy or loweralkyl;
- W.sub.f is C.dbd.O or CHOH;
- U.sub.f is CH.sub.2 or NR.sub.2f provided that when W.sub.f is CHOH then U.sub.f is CH.sub.2 ;
- R.sub.1f is loweralkyl, cycloalkylmethyl, benzyl, 4-methoxybenzyl, halobenzyl, (1-naphthyl)methyl, (2-naphthyl)methyl, (4-imidazolyl)methyl, (alpha,alpha)dimethylbenzyl, 1-benzyloxyethyl, phenethyl, phenoxy, thiophenoxy, or anilino;
- provided that when R.sub.1f is phenoxy, thiophenoxy or anilino, then B.sub.f is CH.sub.2 or CHOH or A.sub.f is hydrogen;
- R.sub.2f is hydrogen or loweralkyl;
- R.sub.3f is loweralkyl, loweralkenyl,((alkoxy)alkoxy)loweralkyl, (thioalkoxy)alkyl, benzyl or heterocyclic ring substituted methyl;
- R.sub.6f is loweralkyl, cycloalkylmethyl or benzyl;
- R.sub.af is vinyl, formyl, hydroxymethyl or hydrogen;
- R.sub.df is hydrogen or loweralkyl;
- R.sub.bf and Ref are independently selected from OH and NH.sub.2 ;
- and
- R.sub.cf is hydrogen, loweralkyl, vinyl or arylalkyl;
- or a pharmaceutically acceptable salt, ester or prodrug thereof.
A method for treating or inhibiting renal dysfunction in a human comprising administering to said human a therapeutically effective amount of H-((beta,betadimethyl)-beta-Ala)-(4-OCH.sub.3)Phe-His amide of 2(S)-amino-1-cyclohexyl-3(R),4(S)-dihydroxy-6-methylheptane or a pharmaceutically acceptable salt, ester or prodrug thereof.
A method for treating or inhibiting renal dysfunction in a human comprising administering to said human a therapeutically effective amount of 2(S)-2-Benzyl-3-(1-methylpiperazin-4-ylsulfonyl)-propionyl-(L)-(4-thiazoly l)Ala amide of (2S,3R,4S)-2-amino-1-cyclohexyl-3,4-dihydroxy-6-methylheptane or a pharmaceutically acceptable salt, ester or prodrug thereof.
Dependencies are inferred from the claim text.