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Amido compounds and their use as pharmaceuticals

a technology of amido compounds and amido amine, which is applied in the field of modulators of 11 hydroxyl steroid dehydrogenase, and achieves the effects of reducing the number of adipose tissue,

Inactive Publication Date: 2007-08-02
INCYTE CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The present invention provides compounds that can modulate the activity of certain proteins (such as 11βHSD1 and MR) and treat diseases associated with their activity. These compounds can be administered as pharmaceutical agents or in other forms. The technical effect of this invention is the development of new tools for research and treatment of diseases associated with the activity of certain proteins.

Problems solved by technology

It is now clear that elevated levels of aldosterone are associated with deleterious effects on the heart and kidneys, and are a major contributing factor to morbidity and mortality in both heart failure and hypertension.
When challenged with oral cortisone, CRD patients exhibit abnormally low plasma cortisol concentrations.
However, the role of glucocorticoids in prevalent forms of human obesity has remained obscure because circulating glucocorticoid concentrations are not elevated in the majority of metabolic syndrome patients.
One particular complication with these treatment regimens is corticosteroid-induced glaucoma.
In its most advanced and untreated form, IOP can lead to partial visual field loss and eventually blindness.
Glucocorticoids can have adverse effects on skeletal tissues.

Method used

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  • Amido compounds and their use as pharmaceuticals
  • Amido compounds and their use as pharmaceuticals
  • Amido compounds and their use as pharmaceuticals

Examples

Experimental program
Comparison scheme
Effect test

example 1

(3S)-1-((1-(4-Chlorophenyl)cyclopropyl)carbonyl)pyrrolidin-3-ol

[0250] To a solution of 1-(4-chlorophenyl)cyclopropanecarboxylic acid (50 mg, 0.25 mmol), (3S)-pyrrolidin-3-ol (24.4 mg, 0.28 mmol) and BOP (116.0 mg, 0.26 mmol) in 0.4 mL DMF was added hunig base (0.066 ml, 0.38 mmol). The mixture was stirred at room temperature overnight and directly purified by prep. HPLC to provide (3S)-1-((1-(4-chlorophenyl)cyclopropyl)carbonyl)pyrrolidin-3-ol (20 mg). LCMS: m / z 266.0 (M+H)+; 553.1 (2M+Na)+.

example 2

(3S)-1-[(1-Phenylcyclopropyl)carbonyl]pyrrolidin-3-ol

[0251] This compound was prepared using procedures analogous to those described for Example 1. LCMS: m / z232.1 (M+H)+.

example 3

(3R)-1-[(1-Phenylcyclopropyl)carbonyl]pyrrolidin-3-ol

[0252] This compound was prepared using procedures analogous to those described for Example 1. LCMS: m / z 232.1 (M+H)+.

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Abstract

The present invention relates to inhibitors of 11-β hydroxyl steroid dehydrogenase type 1, antagonists of the mineralocorticoid receptor (MR), and pharmaceutical compositions thereof. The compounds of the invention can be useful in the treatment of various diseases associated with expression or activity of 11-β hydroxyl steroid dehydrogenase type 1 and / or diseases associated with aldosterone excess.

Description

CROSS REFERENCE TO RELATED APPLICATIONS [0001] This application claims the benefit of U.S. Ser. No. 60 / 569,273, filed May 7, 2004; Ser. No. 60 / 602,051, filed Aug. 17, 2004; Ser. No. 60 / 602,791, filed Aug. 19, 2004; and Ser. No. 60 / 638,803, filed Dec. 22, 2004, the disclosures of each of which are incorporated herein by reference in their entireties.FIELD OF THE INVENTION [0002] The present invention relates to modulators of 11-β hydroxyl steroid dehydrogenase type 1 (11βHSD1) and / or mineralocorticoid receptor (MR), compositions thereof and methods of using the same. BACKGROUND OF THE INVENTION [0003] Glucocorticoids are steroid hormones that regulate fat metabolism, function and distribution. In vertebrates, glucocorticoids also have profound and diverse physiological effects on development, neurobiology, inflammation, blood pressure, metabolism and programmed cell death. In humans, the primary endogenously-produced glucocorticoid is cortisol. Cortisol is synthesized in the zona fas...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/5375A61K31/496A61K31/495A61K31/445A61K31/401C07D207/06C07D207/08C07D207/10C07D207/12C07D207/14C07D207/16C07D207/263C07D207/30C07D209/08C07D209/42C07D209/44C07D209/52C07D209/62C07D209/70C07D211/16C07D211/18C07D211/22C07D211/34C07D211/46C07D211/48C07D211/52C07D211/58C07D211/64C07D211/66C07D211/70C07D213/38C07D217/06C07D217/26C07D221/00C07D221/20C07D223/02C07D223/04C07D231/04C07D295/185C07D333/34C07D401/04C07D401/06C07D401/10C07D401/14C07D403/04C07D405/04C07D405/14C07D413/10C07D413/14C07D417/04C07D471/04C07D471/10C07D487/04C07D487/08C07D487/10C07D491/10C07D491/20C07D493/10C07D495/04C07D498/20C07D513/10
CPCC07D207/06C07D513/10C07D207/10C07D207/12C07D207/14C07D207/16C07D207/27C07D209/08C07D209/42C07D209/44C07D209/52C07D209/62C07D209/70C07D211/16C07D211/18C07D211/22C07D211/34C07D211/46C07D211/48C07D211/52C07D211/58C07D211/64C07D211/66C07D211/70C07D213/38C07D217/06C07D217/26C07D221/20C07D295/185C07D333/34C07D401/04C07D401/06C07D401/10C07D401/14C07D403/04C07D405/04C07D405/14C07D413/10C07D413/14C07D417/04C07D471/04C07D471/10C07D487/04C07D487/08C07D487/10C07D491/10C07D491/20C07D493/10C07D495/04C07D498/20C07D207/08C07D491/107A61P11/04A61P13/12A61P19/10A61P25/28A61P27/02A61P27/06A61P29/00A61P3/00A61P3/04A61P3/06A61P3/08A61P43/00A61P5/48A61P5/50A61P7/00A61P7/02A61P9/00A61P9/04A61P9/10A61P9/12A61P9/14A61P3/10A61K31/438A61K31/4439A61K31/407
Inventor YAO, WENQINGZHUO, JINCONGXU, MEIZHONGMETCALF, BRIAN W.HE, CHUNHONGQIAN, DING-QUANZHANG, COLIN
Owner INCYTE CORP
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