[EN] HETEROCYCLIC DERIVATIVES AS IAP BINDING COMPOUNDS [FR] DÉRIVÉS HÉTÉROCYCLIQUES CONVENANT COMME COMPOSÉS SE LIANT AUX INHIBITEURS DE PROTÉINES D'APOPTOSE
Unprecedented CuI/CuII‐assisted tandem catalysis allowing an Ullmann/Chan–Evans–Lam sequence was achieved. This three‐component, one‐pot reaction triggered by a change in the oxidation state of the metal leads to the selective N1,N3‐diarylation of 3‐aminopyrazole. This new method should be a valuable tool for small‐molecule drug discovery that requires suitable regio‐ and/or chemoselective strategies
前所未有的Cu I / Cu II辅助串联催化,实现了Ullmann / Chan–Evans–Lam序列。这种由金属的氧化态变化引发的三组分一锅法反应导致3-氨基吡唑的选择性N 1,N 3-二芳基化。这种新方法应该是发现小分子药物的有价值的工具,它需要适当的区域和/或化学选择策略来使含氮杂环的N-芳基化。
Inhibitors of IAP
申请人:Cohen Frederick
公开号:US20060014700A1
公开(公告)日:2006-01-19
The invention provides novel inhibitors of IAP that are useful as therapeutic agents for treating malignancies where the compounds have the general formula I:
wherein X, Y, A, R
1
, R
2
, R
3
, R
4
, R
4
′, R
5
, R
5
′, R
6
and R
6
′ are as described herein.
The invention provides novel inhibitors of IAP that are useful as therapeutic agents for treating malignancies where the compounds have the general formula I:
wherein X, Y, A, R
1
, R
2
, R
3
, R
4
, R
4
′, R
5
, R
5
′, R
6
and R
6
′ are as described herein.
The present invention relates to compounds of formula (I), or pharmaceutically acceptable salts, solvates or prodrugs thereof, that bind to Inhibitor of Apoptosis Proteins (IAPs). The compounds of the invention may be used as diagnostic and therapeutic agents in the treatment of proliferative diseases, such as cancer, for promoting apoptosis in proliferating cells, and for sensitizing cells to inducers of apoptosis. The present invention furthermore provides a polymeric compound of formulas (VI) or (VII), comprising either at least two monomeric units of compounds of formula (I), or at least one monomeric unit of a compound of formula (I) and an entity E. The present invention further relates to pharmaceutical compositions comprising said compounds of formulas (I), (VI), and (VII) and the use of said compounds in medicine.