US2010331549A1PendingUtilityA1
Novel compounds useful for modulating abnormal cell proliferation
Est. expirySep 14, 2024(expired)· nominal 20-yr term from priority
C07D 213/57C07D 307/54C07D 213/40C07C 255/41C07D 333/24A61P 35/02A61P 35/00
41
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
There is described compounds of Formulæ I, II, III, IV and V. The compounds of Formulæ I, II, III, IV and/or V are useful: in therapeutic methods and compositions for modulating cell proliferation, in diagnostic assays and as research tools.
Claims
exact text as granted — not AI-modified1 - 7 . (canceled)
8 . A compound of Formula III, and salts, solvates and hydrates thereof:
wherein:
R 1 is selected from OH, OC 1-6 alkyl, NO 2 ;
R 2 is selected from H, OH, C 1-6 alkyl, OC 1-6 alkyl, OC(O)C 1-6 alkyl, C(O)OC 1-6 alkyl, NH 2 , NH—C 1-6 alkyl, N(C 1-6 alkyl)(C 1-6 alkyl), C(O)NHC 1-6 alkyl, C(O)N(C 1-6 alkyl)(C 1-6 alkyl), SH, SC 1-6 alkyl, NO 2 ; CF 3 , OCF 3 and halo;
R 3 is selected from C(X) R 4 , SO 2 Ar, NH 2 , NHC 1-6 alkyl, N(C 1-6 alkyl)(C 1-6 alkyl), P(O)(OH) 2 , P(O)(OC 1-6 alkyl) 2 , and C(NH 2 )═C(CN) 2 ;
R 4 is selected from NH 2 , OH, OC 1-6 alkyl, OAr, NHAr, NH(CH 2 ) n Ar, NH(CH 2 )—OH, (CH 2 ) n OC 1-6 alkyl, C 1-6 alkyl, NHNH 2 , NHC(O)NH 2 , NHC(O)C 1-6 alkoxy, N-morpholino and N-pyrrolidino;
Ar is an aromatic or heteroaromatic group, unsubstituted or substituted with 1-4 substituents independently selected from OH, C 1-6 allyl, C 1-6 alkoxy, C 1-3 alkylenedioxy, NH 2 , NH—C 1-6 alkyl, N(C 1-6 alkyl)(C 1-6 alkyl), SH, NO 2 , CF 3 , OCF 3 and halo;
X is selected from O and S;
Y is selected from (CH 2 CH 2 O) p ;
n is 1 to 6; and
p is 1 to 3.
9 . (canceled)
10 . (canceled)
11 . (canceled)
12 . A compound of Formula IV, and salts, solvates and hydrates thereof:
wherein:
A is a ring chosen from benzene, pyridine, pyrasine, pyrimidine, imidazole, furan and thiophene, unsubstituted or substituted with 1-4 substituents independently selected from OH C 1-6 alkyl, C 1-6 alkoxy, C 1-3 alkylenedioxy, NH 2 , NH—C 1-6 alkyl, N(C 1-6 alkYl)(C 1-6 alkyl), SH, S—C 1-6 alkyl, NO 2 , CF 3 , OCF 3 and halo;
B is a ring chosen from benzene and pyridine;
R 1 is selected from C(X) R 2 , SO 2 Ar, NH 2 , NHC 1-6 alkyl, N(C 1-6 alkyl)(C 1-6 alkyl), P(O)(OH) 2 , P(O)(OC 1-6 alkyl) 2 , and C(NH 2 )═C(CN) 2 ;
R 2 is selected from NH 2 , OH, OC 1-6 alkyl, OAr, OYC 1-3 alkyl, NHAr, NH(CH 2 ) n Ar, NH(CH 2 ) n OH, (CH 2 )—OC 1-6 alkyl, C 1-6 alkyl, C 1-6 alkoxy, NHNH 2 , NHC(O)NH 2 , NHC(O)C 1-6 alkoxy, N-morpholino and N-pyrrolidino;
Ar is an aromatic or heteroaromatic group, unsubstituted or substituted with 1-4 substituents independently selected from OH, C 1-6 alkyl, C 1-6 alkoxy, C 1-3 alkylenedioxy, NH 2 , NH—C 1-6 alkyl, N(C 1-6 alkyl)(C 1-6 alkyl), SH, S—C 1-6 alkyl, NO 2 , CF 3 , OCF 3 and halo;
X is selected from O and S;
Y is selected from (CH 2 CH 2 O) p ;
n is 1 to 6; and
p is 1 to 3.
13 . (canceled)
14 . (canceled)
15 . (canceled)
16 . A compound of Formula V, and salts, solvates and hydrates thereof:
wherein:
R 1 , R 2 and R 3 are each independently selected from OH, C 1-6 alkyl, OC 1-6 alkyl, OC(O)C 1-6 alkyl, C(O)OC 1-6 alkyl, NH 2 , N(C 1-6 alkyl)(C 1-6 alkyl), C(O)NHC 1-6 alkyl, C(O)N(C 1-6 alkyl)(C 1-6 alkyl), SH, SC 1-6 alkyl, NO 2 , CF 3 , OCF 3 and halo;
R 4 is selected from C(X) R 5 , SO 2 Ar, NH 2 , NHC 1-6 alkyl, N(C 1-6 alkyl)(C 1-6 alkyl), P(O)(OH) 2 , P(O)(OC 1-6 alkyl) 2 , and C(NH 2 )═C(CN) 2 ;
R 5 is selected from NH 2 , OH, OC 1-6 alkyl, OAr, OYC 1-3 alkyl, NHAr, NH(CH 2 ) n Ar, NH(CH 2 ) n OH, (CH 2 ) n OC 1-6 alkyl, C 1-6 alkyl, C 1-6 alkoxy, NHNH 2 , NHC(O)NH 2 , NHC(O)C 1-6 alkoxy, N-morpholino and N-pyrrolidino;
Ar is an aromatic or heteroaromatic group, unsubstituted or substituted with 1-4 substituents independently selected from OH, C 1-6 alkyl, C 1-6 alkoxy, C 1-3 alkylenedioxy, NH 2 , NH—C 1-6 alkyl, N(C 1-6 alkyl)(C 1-6 alkyl), SH, S—C 1-6 alkyl, NO 2 , CF 3 , OCF 3 and halo;
X is selected from O and S;
Y is selected from (CH 2 CH 2 O) p ;
n is 1 to 6; and
p is 1 to 3.
17 - 38 . (canceled)Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.