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Substituted Heteroaryl- and Phenylsulfamoyl Compounds

a technology of phenylsulfamoyl and heteroaryland, which is applied in the field of substituting heteroaryland phenylsulfamoylcompounds, can solve the problems of limiting the use of clinically available hypoglycemic agents, large segments of western populations are now realized to be at particularly high risk, and achieves the reduction of ketone body levels, milk quality, and milk quality.

Inactive Publication Date: 2006-11-16
PFIZER INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0043] Another aspect of the invention is the use of a compound of formula I, in the manufacture of a medicament for the palliative, prophylactic or curative treatment of negative energy balance or a ruminant disease associated with negative energy balance in ruminants, wherein the excessive accumulation of triglycerides in liver tissue is prevented or alleviated, and / or the excessive elevation of non-esterified fatty acid levels in serum is prevented or alleviated.
[0045] Another aspect of the invention is the use of a compound of formula I, in the improvement of fertility, including decreased return to service rates, normal oestrus cycling, improved conception rates, and improved foetal viability.
[0057] Another aspect of the invention is the use of the compound of formula I in the manufacture of a medicament for the palliative, prophylactic or curative treatment of negative energy balance in ruminants and to increase ruminant milk quality and / or milk yield, in a preferred aspect of the invention, the milk quality increase is seen in a reduction in the levels of ketone bodies in ruminant milk.
[0058] In another aspect of the invention, peak milk yield is increased.

Problems solved by technology

As a result, large segments of Western populations are now realized to be at particularly high risk.
The administration of an excess dose of insulin causes hypoglycemia, with effects ranging from mild abnormalities in blood glucose to coma, or even death.
However, the clinically available hypoglycemic agents can have side effects that limit their use.
Moreover, negative energy balance (NEB) is a problem frequently encountered in ruminants particularly dairy cows.
Furthermore, the capacity of the ruminant liver for synthesising very low density lipoproteins to export triglycerides from the liver is limited.
Significantly, if NEFA uptake by the bovine liver becomes excessive, accumulation of ketone bodies can lead to ketosis, and excessive storage of triglycerides may lead to fatty liver.
Fatty liver can lead to prolonged recovery for other disorders, increased incidence of heath problems, and development of “downer cows” that die.
It usually results from increased esterification of NEFA absorbed from blood coupled with the low ability of ruminant liver to secrete triglycerides as very low-density lipoproteins.

Method used

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  • Substituted Heteroaryl- and Phenylsulfamoyl Compounds
  • Substituted Heteroaryl- and Phenylsulfamoyl Compounds
  • Substituted Heteroaryl- and Phenylsulfamoyl Compounds

Examples

Experimental program
Comparison scheme
Effect test

example 1

5-(4-Benzyloxy-phenylsulfamoyl)-2-methyl-benzoic acid

[0467]

[0468] To a solution of 5-chlorosulfonyl-2-methylbenzoic acid (200 mg, 0.85 mmol) and p-benzyloxyaniline (187 mg, 0.94 mmol) in 6 ml acetone and 3 ml dimethylformamide was added a solution of sodium bicarbonate (215 mg, 0.56 mmol) in 2 ml water. The resulting mixture was stirred overnight at room temperature. The acetone was then removed under reduced pressure and the residual mixture gas partitioned between 25 ml 1N aqueous hydrochloric acid solution and 25 ml ethyl acetate. The aqueous phase was separated and extracted with 2×25 ml ethyl acetate. The combined ethyl acetate extracts were dried (anhydrous sodium sulfate) and concentrated under reduced pressure. The residue was purified by flash column chromatography (silica gel, 15 gm) eluting with 9:1 chloroform / methanol to yield a white solid (154 mg). The solid was triturated with dichloromethane to yield the title compound (93 mg, 28% yield) as a white solid. MS: 395.6 ...

example 2

2-Methyl-5-[4-(6-methyl-benzothiazol-2-yl)-phenylsulfamoyl]benzoic acid

[0470]

[0471] 8% yield. MS: 439.4 (M+1) 1H NMR (400 MHz, CD3OD): δ2.44 (s, 3H), 2.53 (s, 3H), 7.23 (m, 2H), 7.29 (m, 1H), 7.34 (m 1H), 7.72 (m, 1H), 7.75 (m, 1H), 7.80 (m, 1H), 7.88 (m, 2H), 8.19 (m, 1H).

example 3

2-Methyl-5-[4-(5-methyl-benzooxazol-2-yl)-phenylsulfamoyl]benzoic acid

[0472]

[0473] 4% yield. MS: 423.4 (M+1); 1H NMR (400 MHz, CD3OD); δ2.42 (s, 3H), 2.51 (s, 3H), 7.17 (m, 1H), 7.26 (m, 2H), 7.35(m, 1H), 7.44 (m, 2H), 7.56 (m, 1H) 8.0 (m, 2H), 8.15 (m, 1H).

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Abstract

The present invention is directed at substituted heteroaryl and phenylsulfamoyl compounds, pharmaceutical compositions containing such compounds and the use of such compounds as peroxisome proliferator actuator receptor (PPAR) agonists. PPAR alpha activators, pharmaceutical compositions containing such compounds and the use of such compounds to elevate certain plasma lipid levels, including high density lipoprotein-cholesterol and to lower certain other plasma lipid levels, such as LDL-cholesterol and triglycerides and accordingly to treat diseases which are exacerbated by low levels of HDL cholesterol and / or high levels of LDL-cholesterol and triglycerides, such as atherosclerosis and cardiovascular diseases, in mammals, including humans. The compounds are also useful for the treatment of negative energy balance (NEB) and associated diseases in ruminants.

Description

BACKGROUND OF INVENTION [0001] The present invention relates to substituted heteroaryl- and phenylsulfamoyl-compounds, pharmaceutical compositions containing such compounds and the use of such compounds as peroxisome proliferator activator receptor (PPAR) agonists. The subject compounds are particularly useful as PPARα agonists and to treat atherosclerosis, hypercholeasterolemia, hypertriglyceridemia, diabetes, obesity, osteoporosis and Syndrome X (also known as metabolic syndrome) in mammals, including humans. The compounds are also useful for the treatment of negative energy balance (NEB) and associated diseases in ruminants. [0002] Atherosclerosis, a disease of the arteries, is recognized to be the leading cause of death in the United States and Western Europe. The pathological sequence leading to atherosclerosis and occlusive heart disease is well known The earliest stage in this sequence is the formation of “fatty streaks” in the carotid, coronary and cerebral arteries and in t...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/423A61K31/195C07D263/60C07C311/45C07C311/21C07C311/44C07C323/49C07D213/75C07D215/12C07D231/12C07D231/56C07D233/68C07D235/18C07D263/32C07D263/54C07D263/56C07D263/57C07D271/06C07D271/07C07D271/10C07D271/107C07D271/113C07D277/24C07D277/26C07D277/62C07D277/66C07D285/01C07D285/06C07D307/79C07D333/58C07D413/06
CPCC07C311/21C07D413/06C07C323/49C07C2101/04C07C2101/14C07D213/75C07D215/12C07D231/12C07D231/56C07D233/68C07D263/32C07D263/57C07D271/06C07D271/07C07D271/10C07D271/107C07D271/113C07D277/24C07D277/26C07D277/62C07D277/66C07D285/01C07D285/06C07D307/79C07D333/58C07C311/44C07C2601/04C07C2601/14A61P13/12A61P19/06A61P19/10A61P25/28A61P29/00A61P3/04A61P3/06A61P3/08A61P43/00A61P9/00A61P9/04A61P9/10A61P9/12A61P9/14A61P3/10
Inventor HAMANAKA, ERNESTKEHRLI, MARCUS
Owner PFIZER INC
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