[EN] SPIROBARBITURIC ACID DERIVATIVES USEFUL AS INHIBITORS OF MATRIX METALLOPROTEASES<br/>[FR] DERIVES D'ACIDE SPIROBARBITURIQUE UTILES EN TANT QU'INHIBITEURS DE METALLOPROTEASES DE MATRICE (MMP)
申请人:BRISTOL MYERS SQUIBB CO
公开号:WO2003091252A1
公开(公告)日:2003-11-06
Compound having the formula (I),wherein A, B and D are O or S; R1a and R1b are H, C1-4 alkyl, C2-4alkenyl; X is-NR2-,-S-,-S(=O)-, or -S(O)2-; G1, G2 and G3 are together or separately selected from hetero, carbonyl, alkylene, and alkenylene groups and G4 is optionally substituted methylene; R2 is Q-Ar, wherein Q is a linker and Ar is substituted or substituted aryl or heteroaryl; and z is 0 or 1, are useful as inhibitors of MMPs, particularly MMP-13, aggrecanase, and/or TACE.
Spirobarbituric acid derivatives useful as inhibitors of matrix metalloproteases
申请人:——
公开号:US20040024001A1
公开(公告)日:2004-02-05
Compound having the formula (I),
1
wherein A, B and D are O or S; R
1a
and R
1b
are H, C
1-4
alkyl, C
2-4
alkenyl, or C
2-4
alkynyl; X is —NR
2
—, —S—, —S(═O)—, or —S(O)
2
—; G
1
, G
2
and G
3
are together or separately selected from hetero, carbonyl, alkylene, and alkenylene groups and G
4
is optionally substituted methylene; R
2
is Q-Ar, wherein Q is a linker and Ar is substituted or substituted aryl or heteroaryl; and z is 0 or 1, are useful as inhibitors of MMPs, particularly MMP-13, aggrecanase, and/or TACE.
具有式(I)的化合物、
1
其中 A、B 和 D 为 O 或 S;R
1a
和 R
1b
是 H、C
1-4
烷基、C
2-4
烯基,或 C
2-4
炔基;X 是 -NR
2
-、-S-、-S(═O)- 或 -S(O)
2
-; G
1
, G
2
和 G
3
共同或分别选自杂基、羰基、亚烷基和烯基,以及 G
4
是任选取代的亚甲基
2
是 Q-Ar,其中 Q 是连接基,Ar 是取代或被取代的芳基或杂芳基;以及 z 是 0 或 1。
Casadei, Maria Antonietta; Gessner, Andreas; Inesi, Achille, Bulletin de la Societe Chimique de France, 1989, # 5, p. 650 - 656
作者:Casadei, Maria Antonietta、Gessner, Andreas、Inesi, Achille、Jugelt, Werner、Liebezeit, Hannelore、Micheletti Moracci, Franco
DOI:——
日期:——
CASADEI, MARIA ANTONIETTA;GESSNER, ANDREAS;INESI, ACHILLE;JUGELT, WERNER;+, BULL. SOC. CHIM. FR.,(1989) N, C. 650-656
作者:CASADEI, MARIA ANTONIETTA、GESSNER, ANDREAS、INESI, ACHILLE、JUGELT, WERNER、+
1-(4-Methoxypheny])azetidin-2-ones 5a–5g were acetoxylated by lead(IV) acetate to afford the corresponding compounds 6a, 6b, 6c' and 6d–6g. In the d series elimination products 9 and 10 were also formed. Ring homologue 7a afforded the hydrotylated derivative 8'a.