发明名称 Peptoid compounds useful as antibiotics
摘要 <p>A compound of the formula (I): wherein A is an aromatic or heteroaromatic ring system or partially or fully reduced derivatives thereof; Q is hydrogen, C 1 -C 12 straight chain, branched or cyclic alkyl substituted with one or more hydroxy groups, or a mono- or di-saccharide moiety; Z is -CR 10 R 11 -, -NR 12 -, -C(O)O-, -C(O)NR 12 - or -O-, where R 10 and R 11 are independently selected from hydrogen, hydroxy, C 1 -C 6 alkyl, C 6 -C 10 aryl, C 1 -C 6 alkoxy and -N(R 13 ) 2 and where each R 13 is independently selected from hydrogen and C 1 -C 6 alkyl, and where R 12 is selected from hydrogen and C 1 -C 6 alkyl; R 1 is selected from hydrogen, hydroxy, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, -NR(R 13 ) 2 and -N(R 12 )-COR 14 ; where R 12 and R 13 are as defined above, and where R 14 is selected from hydrogen, hydroxy, C 1 -C 6 alkyl, C 1 -C 6 alkoxy and -NR 12 ; R 2 is selected from hydrogen, hydroxy, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, -N(R 13 ) 2 and -N(R 12 )-COCHR 2a R 2b ; where R 2a and R 2b are selected from hydrogen, hydroxy, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, -N(R 13 ) 2 and -N(R 12 )-COR 14 ; where R 12 , R 13 and R 14 are as defined above; R 3 , R 4 and R 5 are independently selected from hydrogen, C 1 -C 6 alkyl and ± side chains of ±-amino acids or their enantiomers or their derivatives; R 6 is -CO 2 R 15 , -CONHR 16 , -CONHOR 16 , -CONHNHR 16 , -SO 2 N(R 16 ) 2 , -SO 2 R 17 or -P(O)(OR 18 )(OR 18 ) where each R 15 , R 16 , R 17 and R 18 is independently selected from hydrogen, C 1 -C 6 alkyl, C 3 -C 7 cycloalkyl, C 6 -C 10 aryl and C 7 -C 10 arylalkyl; B is an ±-amino acid residue, a ²-amino acid residue or an ±,±-disubstituted amino acid residue, such residue forming amide linkages with the adjacent molecules; W is -O- or CR 10 R 11 where R 10 and R 11 are as defined above; Y is an optionally substituted amino group, a moiety containing an optionally substituted amino group or a salt thereof: ------ is a single or double bond; R 7 and R 8a are hydrogen or are absent if ------ is a double bond; and R 8b and R 9 are hydrogen, and X is selected from (CR 10 R 11 ) u , -(CR 10 R 11 ) u -CH=CH-, -NR 12 (CR 10 R 11 ) u -, -(CR 10 R 11 ) u NR 12 -, -O(CR 10 R 11 ) u -, -(CR 10 R 11 ) u O- or -O(CR 10 R 11 )CH=CH- where R 10 , R 11 and R 12 are as defined above; or R 8b and R 9 together form a covalent bond between X and the carbon to which R 8b is attached, and X is selected from (CR 10 R 11 ) x , -NR 12 (CR 10 R 11 ) x -, -(CR 10 R 11 ) x NR 12 -, -O(CR 10 R 11 ) x - or -(CR 10 R 11 ) x O-, where R 10 , R 11 and R 12 are as defined above; n, m, r and t are independently selected from 0 or 1; s is an integer selected from 0 to 3; p is an integer selected from 0 to 6, provided that when W is -O-, p is at least 1; and u, x and q are independently selected from 0 to 4; and salts and pharmaceutically acceptable derivatives thereof. The compound of formula (I) are useful in the treatment of bacterial infections.</p>
申请公布号 EP2343285(B1) 申请公布日期 2015.02.25
申请号 EP20110158209 申请日期 2002.06.28
申请人 UNIVERSITY OF WOLLONGONG 发明人 BREMNER, JOHN;PYNE, STEPHEN;KELLER, PAUL;COGHLAN, DAN;GARAS, ADEL;WITCHARD, HELEN;BOYLE, TIM;COATES, JONATHAN
分类号 A61K38/00;C07D245/04;A61K38/06;A61K38/12;A61P31/04;C07C229/36;C07C233/31;C07C233/47;C07C237/22;C07C251/24;C07D209/18;C07D209/86;C07D209/88;C07D255/04;C07D273/02;C07D273/08;C07D487/02;C07D487/04;C07K5/02;C07K5/06;C07K5/068;C07K5/08;C07K5/087;C07K5/10;C07K5/107 主分类号 A61K38/00
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