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US5326773A Expired / Lapsed US ⏱️ 0.0 years remaining

Inhibitors of farnesyl-protein transferase

Assignee: Merck and Co Inc
•
Filing: 1992-10-29
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Granted: 1994-07-05
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Expires: 2012-10-29
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Abstract

Abstract The present invention is directed to compounds which inhibit farnesyl-protein transferase (FTase) and the farnesylation of the oncogene protein Ras. The invention is further directed to chemotherapeutic compositions containing the compounds of this invention and methods for inhibiting farnesyl-protein transferase and the farnesylation of the oncogene protein Ras.

Inventors

  • 👤 S. Jane de Solms
  • 👤 Samuel L. Graham

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-08 12:55
CPC Classifications
C; C07; C07C; C07C321/00; C07C321/02; C07C321/04; C07K; C07K5/00; C07K5/04; C07K5/06; C07K5/06008; C07K5/06078; A; A61; A61P; A61P35/00; C07D; C07D305/00; C07D305/02; C07D305/10; C07D305/12; C07D309/00; C07D309/16; C07D309/28; C07D309/30; C07K5/06017; C07K5/06034; C07K5/06052; A61K; A61K38/00

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 173 words
A prodrug of the formula IV: ##STR13## R 1 is hydrogen, an alkyl group, an aralkyl group, an acyl group, an aracyl group, an aroyl group, an alkylsulfonyl group, aralkylsulfonyl group or arylsulfonyl group, wherein alkyl and acyl groups comprise straight chain or branched chain hydrocarbons of 1 to 6 carbon atoms; R 2 and R 3 are the side chains of naturally occurring amino acids, and their oxidized forms which may be methionine sulfoxide or methionine sulfone, or in the alternative may be substituted or unsubstituted aliphatic, aromatic or heteroaromatic groups, comprising allyl, cyclohexyl, phenyl, pyridyl, imidazolyl or saturated chains of 2 to 8 carbon atoms which may be branched or unbranched, wherein the aliphatic substitutents may be substituted with an aromatic or heteroaromatic ring; R 5 is an alkyl group, wherein the alkyl group comprises straight chain or branched chain hydrocarbons of 1 to 6 carbon atoms, which may be substituted with an aromatic or heteroaromatic group; n is 0, 1 or 2; and the pharmaceutically acceptable salts and disulfides thereof.
Claim 2
Dependent Claim 173 words
A prodrug of the formula IV: ##STR13## R 1 is hydrogen, an alkyl group, an aralkyl group, an acyl group, an aracyl group, an aroyl group, an alkylsulfonyl group, aralkylsulfonyl group or arylsulfonyl group, wherein alkyl and acyl groups comprise straight chain or branched chain hydrocarbons of 1 to 6 carbon atoms; R 2 and R 3 are the side chains of naturally occurring amino acids, and their oxidized forms which may be methionine sulfoxide or methionine sulfone, or in the alternative may be substituted or unsubstituted aliphatic, aromatic or heteroaromatic groups, comprising allyl, cyclohexyl, phenyl, pyridyl, imidazolyl or saturated chains of 2 to 8 carbon atoms which may be branched or unbranched, wherein the aliphatic substitutents may be substituted with an aromatic or heteroaromatic ring; R 5 is an alkyl group, wherein the alkyl group comprises straight chain or branched chain hydrocarbons of 1 to 6 carbon atoms, which may be substituted with an aromatic or heteroaromatic group; n is 0, 1 or 2; and the pharmaceutically acceptable salts and disulfides thereof.
Claim 3
Dependent Claim 7 words
The compound which is: N-[2(S)-(2(R)-amino-3-mercaptopropylamino)-3(S)-methylpentyl]-N-methyl-isoleucyl-homoserine lactone ##STR14##
Claim 4
Dependent Claim 7 words
The compound which is: N-[2(S)-(2(R)-amino-3-mercaptopropylamino)-3(S)-methylpentyl]-N-methyl-isoleucyl-homoserine lactone ##STR14##
Claim 5
Dependent Claim 28 words
A prodrug of a compound which inhibits farnesyl-protein transferase which is: N-{2(S)-(2(R)-amino-3-mercaptopropylamino)-3(S)-methylpentyl}-N-methyl-phenylalanyl-homoserine lactone, N-{2(S)-(2(R)-amino-3-mercaptopropylamino)-3-methyl-butyl}-N-methyl-phenylalanyl-homoserine lactone, 3(S)-{N-{2(S)-(2(R)-amino-3-mercaptopropylamino)-3(s)-methylpentyl}-N-methyl-isoleucylamino}-3-methyltetrahydropyran-2-one, N-[2(S)-(2(R)-amino-3-mercaptopropylamino)-3-(S)-methylpentyl]-N-methyl-norvalyl-homoserine lactone, 3(S)-{N-[2(S)-(2(R)-amino-3-mercaptopropylamino)-3(S)-methylpentyl]-N-methyl-isoleucylamino}-6,6-dimethyltetrahydropyran-2-one, N-[2(S)-(2(R)-amino-3-mercaptopropylamino)-3(S)-methylpentyl]-N-methyl-D-norvalyl-homoserine lactone, and the pharmaceutically salts and disulfides thereof.
Claim 6
Dependent Claim 28 words
A prodrug of a compound which inhibits farnesyl-protein transferase which is: N-{2(S)-(2(R)-amino-3-mercaptopropylamino)-3(S)-methylpentyl}-N-methyl-phenylalanyl-homoserine lactone, N-{2(S)-(2(R)-amino-3-mercaptopropylamino)-3-methyl-butyl}-N-methyl-phenylalanyl-homoserine lactone, 3(S)-{N-{2(S)-(2(R)-amino-3-mercaptopropylamino)-3(s)-methylpentyl}-N-methyl-isoleucylamino}-3-methyltetrahydropyran-2-one, N-[2(S)-(2(R)-amino-3-mercaptopropylamino)-3-(S)-methylpentyl]-N-methyl-norvalyl-homoserine lactone, 3(S)-{N-[2(S)-(2(R)-amino-3-mercaptopropylamino)-3(S)-methylpentyl]-N-methyl-isoleucylamino}-6,6-dimethyltetrahydropyran-2-one, N-[2(S)-(2(R)-amino-3-mercaptopropylamino)-3(S)-methylpentyl]-N-methyl-D-norvalyl-homoserine lactone, and the pharmaceutically salts and disulfides thereof.
Claim 7
Dependent Claim 20 words
A pharmaceutical composition comprising a pharmaceutical carrier, and dispersed therein a therapeutically effective amount of a compound of claim 1.

References Cited (Backward Citations)

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WO1991016340A1 Cited
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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1997-07-04 1998-01-03 1998-07-05 $2000.00 Window Closed / Lapsed
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