发明名称 ALIPHATIC AMINO CARBOXYLIC AND AMINO PHOSPHONIC ACIDS, AMINO NITRILES AND AMINO TETRAZOLES AS CELLULAR RESCUE AGENTS
摘要 1. A compound of the Formula I wherein: R1 is (CH2)mCH3 where m is 0 or an integer in the range from 1 to 16, or an alkenyl, alkynyl, alkoxy, alkylthio, or alkyl sulfinyl group having from 2 to 17 carbon atoms, wherein R1 may be optionally substituted with one or more substituents selected from hydroxy, aldehyde, oxo, lower acyloxy, halogen, thio, sulfoxide and sulfone, R2 = H, CH3 or CH2CH3, R3 = H or CH3, R4 = H or CH3, R5 = lower alkyl having from 1 to 5 carbon atoms, n is an integer in the range from 1 to 3, and X is carboxyl (COOH) or carbalkoxy (COOR5), cyano (C [triple bond] N), phosphonic acid (PO3H2), phosphonate ester (PO3[R5]2) or 5-tetrazole, as a substantially pure enantiomer in the R or S configuration at a carbon atom to which R1, R2 and R3 substituents are attached or a pharmaceutically acceptable salt thereof. 2. A compound of the Formula I according to claim 1 wherein: R1 is (CH2)mCH3 where m is 0 or an integer in the range from 1 to 16, R2 = CH3 wherein R1 and R2 substituents have different meanings, R3 = H, R4 = H or CH3, R5 = lower alkyl having from 1 to 5 carbon atoms, n is an integer in the range from 1 to 3, and X is carboxyl (COOH) or carbalkoxy (COOR5), cyano (C [triple bond] N), phosphonic acid (PO3H2), phosphonate ester (PO3[R5]2) or 5-tetrazole, or a pharmaceutically acceptable salt thereof. 3. A compound of the Formula I according to claim 1 wherein: R1 is (CH2)mCH3 where m is 0 or an integer in the range from 1 to 16, R2 = CH3 wherein R1 and R2 substituents have different meanings, R3 = H, R4 = H or CH3, R5 = lower alkyl having from 1 to 5 carbon atoms, n is an integer in the range from 1 to 3, and X is carboxyl (COOH) or carbalkoxy (COOR5), cyano (C [triple bond] N), phosphonic acid (PO3H2), phosphonate ester (PO3[R5]2) or 5-tetrazole, or a pharmaceutically acceptable salt thereof. 3. A compound of the Formula I according to claim 1 wherein: R1 is (CH2)mCH3 where m is 0 or an integer in the range from 1 to 16, R2 = CH3 wherein R1 and R2 substituents have different meanings, R3 = H, R4 = H or CH3, R5 = lower alkyl having from 1 to 5 carbon atoms, n is an integer in the range from 1 to 3, and X is carboxyl (COOH) or carbalkoxy (COOR5), cyano (C [triple bond] N), phosphonic acid (PO3H2), phosphonate ester (PO3[R5]2) or 5-tetrazole, as a substantially pure enantiomer in the R-configuration, or a pharmaceutically acceptable salt thereof. 4. A compound of the Formula I according to claim 1 wherein: R1 is (CH2)mCH3 where m is 0 or an integer in the range from 1 to 16, R2 = CH3 wherein R1 and R2 substituents have different meanings, R3 = H, R4 = H or CH3, R5 = lower alkyl having from 1 to 5 carbon atoms, n is an integer in the range from 1 to 3, and X is carboxyl (COOH) or carbalkoxy (COOR5), cyano (C [triple bond] N), phosphonic acid (PO3H2), phosphonate ester (PO3[R5]2) or 5-tetrazole, as a substantially pure enantiomer in the S-configuration, or a pharmaceutically acceptable salt thereof. 5. A compound according to claim 3, wherein said compound of formula 1 is selected from the group consisting of: (R)-3-(2-Heptylamino)propionic acid; (R)-3-(2-Heptylmethylamino)propionic acid; Methyl (R)-3-(2-heptylamino)propionate; Methyl (R)-3-(2-heptytmethylamino)propionate; (R)-2-(2-Pentylamino)acetonitrile; (R)-2-(2-Pentylmethylamino)acetonitrile; (R)-3-(2-Heptylamino)propionitrile; (R)-3-(2-Heptylmethylamino)propionitrile; (R)-2-(2-Pentylamino)ethanephosphonic acid; (R)-2-(2-Pentylmethylamino)ethanephosphonic acid; and (R)-2-(2-Heptylamino)ethane-5-tetrazole. 6. A compound according to claim 4, wherein said compound of formula I is selected from the group consisting of: (S)-2-(2-Heptylamino)acetic acid; (S)-2-(2-Heptylmethylamino)acetic acid; Methyl (S)-2-(2-heptylamino)acetate; Methyl (S)-2-(2-heptylmethylamino)acetate; (S)-2-(2-Heptylamino)acetonitrile; (S)-2-(2-Heptylmethylamino)acetonitrile; (S)-2-(2-Heptylamino)ethanephosphonic acid; and (S)-2-(2-Heptylmethylamino)ethanephosphonic acid. 7. A compound selected from the group consisting of: 2-(1-Hexylmethylamino)acetic acid; 3-(2-Propylmethylamino)propionic acid; Methyl 2-(2-propylmethylamino)acetate; Methyl 2-(1-hexylmethylamino)acetate; Methyl 3-(1-hexylmethylamino)propionate; 2-(1-Hexylamino)acetonitrile; 2-(1-Hexylmethylamino)acetonitrile; 3-(3-Pentylamino)propionitrile; 3-(3-Pentylmethylamino)propionitrile; 2-(2-Propylamino)ethanephosphonic acid; and 2-(2-Propylmethylamino)ethanephosphonic acid. 8. A compound according to any one of claims 1 to 7 in the form of a hydrochloride salt. 9. A compound according to any one of claims 1 to 4 wherein m is an integer from 1 to 12. 10. A compound according to any one of claims 1 to 4 wherein m is an integer from 1 to 9. 11. A composition for the treatment or prevention of a disease in which cell death occurs by apoptosis, which composition comprises an effective amount of a compound having the formula I: wherein: R1 is (CH2)mCH3 where m is 0 or an integer in the range from 1 to 16, or an alkenyl, alkynyl, alkoxy, alkylthio, or alkyl sulfinyl group having from 2 to 17 carbon atoms, wherein R1 may be optionally substituted with one or more substituents selected from hydroxy, aldehyde, oxo, lower acyloxy, halogen, thio, sulfoxide and sulfone, R2 = H, CH3 or CH2CH3, R3 = H or CH3, R4 = H or CH3, R5 = lower alkyl having from 1 to 5 carbon atoms, n is an integer in the range from 1 to 3, and X is carboxyl (COOH) or carbalkoxy (COOR5), cyano (C [triple bond] N), phosphonic acid (PO3H2), phosphonate ester (PO3[R5]2) or 5-tetrazole, as a substantially pure enantiomer in the R or S configuration at a carbon atom to which R1, R2 and R3 substituents are attached or a pharmaceutically acceptable salt thereof. 12. A composition according to claim 11, wherein: R1 is (CH2)mCH3 where m is 0 or an integer in the range from 1 to 16, R2 = CH3 wherein R1 and R2 substituents have different meanings, R3 = H, R4 = H or CH3, R5 = lower alkyl having from 1 to 5 carbon atoms, n is an integer in the range from 1 to 3, and X is carboxyl (COOH) or carbalkoxy (COOR5), cyano (C [triple bond] N), phosphonic acid (PO3H2), phosphonate ester (PO3[R5]2) or 5-tetrazole, or a pharmaceutically acceptable salt thereof, in admixture with a suitable diluent or carrier. 13. A composition according to claim 11, wherein said compound of formula I is selected front the group consisting of: (R)-3-(2-Heptylamino)propionic acid; (R)-3-(2-Heptylmethylamino)propionic acid; Methyl (R)-3-(2-heptylamino)propionate; Methyl (R)-3-(2-heptylmethylamino)propionate; (R)-2-(2-Pentylamino) acetonitrile; (R)-2-(2-Pentylmethylamino)acetonitrile; (R)-3-(2-Heptylamino)propionitrile; (R)-3-(2-Heptylmethylamino)propionitrile; (R)-2-(2-Pentylamino)ethanephosphonic acid; (R)-2-(2-Penlylmethylamino)ethanephosphonic acid; and (R)-2-(2-Heptylamino)ethane-5-tetrazole. 14. A composition according to claim 11, wherein said compound of formula I is selected from the group consisting of: (S)-2-(2-Heptylamino)acetic acid; (S)-2-(2-Heptylmethylamino)acetic acid; Methyl (S)-2-(2-heptylamino)acetate; Methyl (S)-2-(2-heptylmethylamino)acetate; (S)-2-(2-Heptylamino)acetonitrile; (S)-2-(2-Heptylmethylamino)acetonitrile; (S)-2-(2-Heptylamino)ethanephosphonic acid; and (S)-2-(2-Heptylmethylamino)ethanephosphonic acid. 15. A composition for the treatment or prevention of a disease in which cell death occurs by apoptosis, which composition comprises an effective amount of a compound selected from the group consisting of: 2-(1-Hexylmethylamino)acetic acid; 3-(2-Propylmethylamino)propionic acid; Methyl 2-(2-propylmethylamino)acetate; Methyl 2-(1-hexylmethylamino)acetate; Methyl 3-(1-hexylmethylamino)propionate; 2-(1-Hexylamino)acetonitrile; 2-(1-Hexylmethylamino)acetonitrile; 3-(3-Pentylamino)propionitrile; 3-(3-Pentylmethylamino)propionitrile; 2-(2-Propylamino)ethanephosphonic acid; and 2-(2-Propylmethylamino)ethanephosphonic acid in admixture with a suitable diluent or carrier. 16. A, composition according to any one of claims 11 to 15, wherein the compound of formula I is in the form of a hydrochloride salt. 17. A use of a compound of the formula I R1 is (CH2)mCH3 where m is 0 or an integer in the range from 1 to 16, or an alkenyl, alkynyl, alkoxy, alkylthio, or alkyl sulfinyl group having from 2 to 17 carbon atoms, wherein R1 may be optionally substituted with one or more substituents selected from hydroxy, aldehyde, oxo, lower acyloxy, halogen, thio, sulfoxide and sulfone, R2 = H, CH3 or CH2CH3, R3 = H or CH3, R4 = H or CH3, R5 = lower alkyl having from 1 to 5 carbon atoms, n is an integer in the range from 1 to 3, and X is carboxyl (COOH) or carbalkoxy (COOR5), cyano (C [triple bond] N), phosphonic acid (PO3H2), phosphonate ester (PO3[R5]2) or 5-tetrazole, as a substantially pure enantiomer in the R or S configuration at a carbon atom to which R1, R2 and R3 substituents are attached or a pharmaceutically acceptable salt thereof, for the treatment or prevention of a disease in which cell death occurs by apoptosis. 18. A use according to claim 17, wherein R1 is (CH2)mCH3 where m is 0 or an integer in the range from 1 to 16, R2 = CH3 R3 = H, R4 = H or CH3, R5 = lower alkyl having from 1 to 5 carbon atoms, n is an integer in the range from 1 to 3, and X is carboxyl (COOH) or carbalkoxy (COOR5), cyano (C [triple bond] N), phosphonic acid (PO3H2), phosphonate ester (PO3[R5]2) or 5-tetrazole, or a pharmaceutically acceptable salt thereof. 19. A use according to claim 17 or 18 wherein the compound of the formula I is a substantially pure enantiomer in the R configuration. 20. A use according to claim 17 or 18 wherein the compound of the Formula I is a substantially pure enantiomer in the S configuration. 21. A use according to claim 17 wherein said compound of Formula I is selected from the group consisting of: 2-(2-Propylamino)acetic acid; 2-(1-Hexylamino)acetic acid; (S)-2-(2-Heptylamino)acetic acid; 3-(2-Propylamino)propionic acid; 3-(1-Hexylamino)propionic acid; (R)-3-(2-Heptylamino)
申请公布号 EA003677(B1) 申请公布日期 2003.08.28
申请号 EA20000000987 申请日期 1999.03.25
申请人 UNIVERSITY OF SASKATCHEWAN TECHNOLOGIES INC. 发明人 PATERSON, ALICK, I.;DYCK, LILIAN, E.;DAVIS, BRUCE, A.;LIU, YA-DONG;DURDEN, DAVID, A.;BOULTON, ALAN, A.
分类号 C07D257/04;A61K31/195;A61K31/215;A61K31/275;A61K31/66;A61P9/00;A61P13/12;A61P25/00;A61P25/14;A61P25/16;A61P25/28;A61P27/02;A61P27/06;A61P43/00;C07C229/12;C07C255/24;C07C255/25;C07F9/38;C07F9/40;(IPC1-7):C07C229/12;A61K31/197;A61K31/221;A61K31/662;A61P3/10;A61P9/10 主分类号 C07D257/04
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