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Smac mimetec

a technology of mimetics and smac, applied in the field of smac mimetics, can solve the problems of increasing the apoptosis of abnormally proliferating cells

Inactive Publication Date: 2012-05-10
MEDIVIR AB
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0010]In a further illustrative embodiment, the invention comprises a method of treating an autoimmune disease, in which the condition is caused or exacerbated by abnormal regulation of apoptosis, in a mammal in need thereof, including, for example, systemic lupus erythematosus, psoriasis, and idiopathic thrombocytopenic purpura (Morbus Werlhof) that comprises internally administering to the animal an effective amount of Compound 15 or a pharmaceutically acceptable salt thereof.

Problems solved by technology

However, in certain disease states, e.g., cancers and other proliferative disorders, IAPs are not adequately antagonized and therefore prevent apoptosis and cause or exacerbate abnormal proliferation and survival.
When administered to animals suffering proliferative disorders, the SMAC mimetics antagonize IAPs, causing an increase in apoptosis among abnormally proliferating cells.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

example 1

Synthesis

[0041]

4-(tert-Butyl-dimethyl-silanyloxy)-pyrrolidine-1,2-dicarboxylic acid 1-benzyl ester (2): A solution of Z-Hyp-OH (1, 300 g, 1.13 mol), TEA (395 mL, 2.83 mol), and DBU (17.2 g, 1.13 mol) in DMF (1.25 L) was stirred in a cold water bath while a suspension of TBS-Cl (188 g, 1.24 mol) in DMF (270 mL) was added slowly at 21-26° C. [Note: moderately exothermic]. The resulting thin suspension was stirred for 22 h at ambient temperature. The reaction mixture was cooled to 2° C. and quenched with water (1.54 L) at ≦26°C. [Note: the pH of the aqueous layer was 8.5-9.0]. MTBE (3 L) was added and the mixture was acidified to pH 3-4 with conc. HCl (168 g) at 17-19° C. The organic layer was separated and washed with water (2×1.5 L). The organic layer was concentrated in vacuo and dried by additional MTBE distillation. Toluene (2×500 mL) was added and distilled to remove moisture to provide 603 g of 2 as a light yellow-colored oil [Note: the water content by KF analysis was 508 ppm]....

examples 2 , 3 , 4

Examples 2, 3, 4, and 5

[0053]Compounds tested in Examples 2, 3, 4, and 5 are shown in Table 1.

TABLE 1CompoundR5R15—CH2CH36-F 2—CH(CH3)CH36-F 3—R—CH(OH)CH36-F 4—S—CH(OH)CH36-F 5—R—CH(OCH3)CH36-F

example 2a

cIAP Degradation Assay

[0054]The concentration inducing degradation of cIAP-1 and cIAP-2 by 50% (IC50) for various compounds was determined by monitoring the disappearance of Green Fluorescent Protein (GFP)-signal in A375 cells. Briefly, A375 cell lines expressing GFP-tagged cIAP-1 and cIAP-2 were generated by transfecting HA2xEGFP-pcDNA3 vector containing either cIAP-1 (A375Gc1) or cIAP-2 (A375Gc2) coding region. 2×104 of A375Gc1 or A375Gc2 cells were grown in 96-well plate and treated with various concentrations of test compounds for 2 h. After incubation, cells were collected by trypsinization and suspended in 150 μl of DMEM-10% FBS. A total of 104 cells were analyzed using a FACScan (Becton Dickinson). GFP fluorescence was monitored by using an excitation filter at 488 nm and emission was measured with a 530 nm filter. IC50 is defined as the concentration of drug at which 50% of GFP signal was inhibited. Results of the cIAP-1 and -2 degradation assay are shown in Table 2.

TABLE 2G...

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Abstract

A SMAC mimetic and pharmaceutical compositions thereof and methods of use.

Description

FIELD OF THE INVENTION[0001]This invention is in the field of SMAC mimetics and compositions and uses thereof to treat proliferative disorders including cancers.BACKGROUND OF THE INVENTION[0002]Inhibitors of Apoptosis Proteins (IAPs) are naturally occurring intra-cellular proteins that suppress caspase-dependent apoptosis. SMAC, also known as DIABLO, is another intracellular protein that functions to antagonize, i.e., inhibit the activity of IAPs. In normal healthy cells, SMAC and IAPs function together to maintain healthy cells. However, in certain disease states, e.g., cancers and other proliferative disorders, IAPs are not adequately antagonized and therefore prevent apoptosis and cause or exacerbate abnormal proliferation and survival.[0003]SMAC mimetics, also known as IAP antagonists, are synthetic small molecules that mimic the structure and IAP antagonist activity of the four N-terminal amino acids of SMAC. (SMAC mimetics are sometimes referred to as IAP antagonists.) When ad...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/404A61P35/00A61P17/06A61P35/02C12N5/02C07D403/14
CPCA61K38/00C07D403/06C07K5/06026C07K5/02A61K45/06C07D403/14A61K38/07Y02P20/55A61K31/404A61K31/555A61K38/05A61P17/06A61P35/00A61P35/02A61P35/04A61P37/00A61P37/02A61P37/06A61P43/00A61P7/00A61P7/04A61K38/03C07K5/06A61N5/062A61N5/10C12N5/0693C12N2500/46
Inventor CONDON, STEPHEN M.DENG, YIJUNLAPORTE, MATTHEW G.RIPPIN, SUSAN R.
Owner MEDIVIR AB
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