Inhibitors of farnesyl protein transferase

Claim 2

A compound which inhibits farnesylprotein transferase of the formula: ##STR7## wherein: X, Y and Z are independently H 2 or O, provided that at least one of these is H 2 ; R 1 is H, an alkyl group, an acyl group, an alkylsulfonyl group or arylsulfonyl group, wherein alkyl and acyl groups comprise straight chain or branched chain hydrocarbons of 1 to 6 carbon atoms, or in the alternative, R 1 NH may be absent; R 2 , R 3 and R 4 are the side chains of naturally occurring amino acids, or in the alternative may be substituted or unsubstituted aliphatic, aromatic or heteroaromatic groups, wherein the aliphatic substitutents may be substituted with an aromatic or heteroaromatic ring; R 5 is H or a straight or branched chain aliphatic group, which may be substituted with an aromatic or heteroaromatic group; or the pharmaceutically acceptable salts thereof.

Claim 3

The compound of claim 1, wherein the compound is: N-(3-phenyl-2(S)-(mercaptopropionylamino)prop-1-yl)isoleucyl-methionine, N-(2(R)-amino-3-mercaptopropyl)isoleucyl-phenyl -alanyl-methionine, N-(3-mercaptopropyl)isoleucyl-phenylalanyl-methionine, N-(3-mercaptopropyl)valyl-isoleucyl-methionine, N-(2(R)-amino-3-mercaptopropyl)valyl-isoleucyl-methionine, N-(3-methyl-2(S)-(cysteinylamino)but-1-yl)phenyl-alanyl-methionine, N-(3-methyl-2(S)-(mercaptopropionylamino)but-1yl)phenylalanyl-methionine, N-[2(S)-(2(R)-amino-3-mercaptopropylamino)-3(S)-methylpentyl]phenylalanyl-methionine, N-[2(S)-(3-mercaptopropylamino)-3(S)-methylpentyl]phenylalanyl-methionine, N-(2(R)-amino-3-mercaptopropyl)isoleucyl-phenyl -alanyl-(methionine sulfone), N-(2(R)-amino-3-mercaptopropyl)isoleucyl-(p-iodo-phenylalanyl)-methionine, N-[2(R)-(cysteinyl-isoleucylamino)-3(S)-methylpentyl]methionine, N-[2(R)-(N'-(2(R)-amino-3-mercaptopropyl)-isoleucylamino)-3-phenyl-propyl]methionine, N-[2(R)-(N'-(2(R)-amino-3-mercaptopropyl)-isoleucylamino)-3(S)-methylpentyl]methionine, N-(3-mercaptopropyl)valyl-isoleucyl-methionine methyl ester, N-(2(R)-amino-3-mercaptopropyl)isoleucyl-phenyl alanyl-methionine ethyl ester, or N-(2(R)-amino-3-mercaptopropyl)isoleucyl-phenyl-alanyl -methionine benzyl ester or the pharmaceutically acceptable salts thereof.

Claim 4

The compound of claim 1 which is: N-[2(S)-(2(R)-amino-3-mercaptopropylamino)-3(S)-methylpentyl]phenylalanyl-methionine ##STR8## or the pharmaceutically acceptable salts thereof.

Claim 5

The compound of claim 1 which is: N-(3-methyl-2(S)-(cysteinylamino)but-1-yl)phenylalanylmethionine ##STR9##

Claim 6

The compound of claim 1 which is: N-(2(R)-amino-3-mercaptopropyl)isoleucyl-phenylalanyl-methionine ethyl ester ##STR10##

Claim 7

A chemotherapeutic composition comprising a pharamaceutical carrier, and dispersed therein, a therapeutically effective amount of a compound of claim 1.

Claim 8

A chemotherapeutic composition comprising a pharmaceutical carrier, and dispersed therein, a therapeutically effective amount of compound of claim 2.

Claim 9

A chemotherapeutic composition comprising a pharmaceutical carrier, and dispersed therein, a therapeutically effective amount of a compound of claim 3.

Claim 10

A chemotherapeutic composition comprising a pharmaceutical carrier, and dispersed therein, a therapeutically effective amount of a compound of claim 4.

Claim 11

A chemotherapeutic composition comprising a pharmaceutical carrier, and dispersed therein, a therapeutically effective amount of a compound of claim 5.

Claim 12

A method for inhibiting farnesylation of Ras protein which comprises administering to a mammal in need thereof a therapeutically effective amount of a composition of claim 6.

Claim 13

A method for inhibiting farnesylation of Ras protein which comprises administering to a mammal in need thereof a therapeutically effective amount of a composition of claim 7.

Claim 14

A method for inhibiting farnesylation of Ras protein which comprises administering to a mammal in need thereof a therapeutically effective amount of a composition of claim 8.

Claim 15

A method for inhibiting farnesylation of Ras protein which comprises administering to a mammal in need thereof a therapeutically effective amount of a composition of claim 9.

Claim 16

A method for inhibiting farnesylation of Ras protein which comprises administering to a mammal in need thereof a therapeutically effective amount of a composition of claim 10.

Claim 17

The method according to claim 11, wherein the mammal is a human.

Claim 18

The method according to claim 12, wherein the mammal is a human.

Claim 19

The method according to claim 13, wherein the mammal is a human.

Claim 20

The method according to claim 14, wherein the mammal is a human.

Claim 21

The method according to claim 15, wherein the mammal is a human.

Claim 22

The compound of claim 1, wherein the substituted or unsubstituted aliphatic, aromatic, or heteroaromatic groups are allyl, cyclohexyl, phenyl, pyridyl, or imidazolyl groups, or are saturated chains of 2 to 8 carbon atoms.