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Antidiabetic agents

a technology of antidiabetic agents and antidiabetic drugs, applied in the field of antidiabetic agents, can solve the problems of limiting their use, hypoglycemic agents can have side effects, and the treatment of diabetes remains less than satisfactory

Inactive Publication Date: 2005-01-27
GAMMILL RONALD B
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

Also provided are kits for the treatment of diabetes, insulin resistance diabetic neuropathy, diabetic nephropathy, diabetic retinopathy, cataracts, hyperglycemia, hypercholesterolemia, hypertension, hyperinsulinemia, hyperlipidemia, atherosclerosis, or tissue ischemia in a patient having diabetes, insulin resistance, diabetic neuropathy, diabetic nephropathy, diabetic retinopathy, cataracts, hyperglycemia, hypercholesterolemia, hypertension, hyperinsulinemia, hyperlipidemia, atherosclerosis, or tissue ischemia, the kits comprising: a) a first pharmaceutical composition comprising a compound of Formula I, stereoisomers, pharmaceutically acceptable salts and prodrugs of the compounds of Formula I, and pharmaceutically acceptable salts of the prodrugs; b) a second pharmaceutical composition comprising a second compound useful for the treatment of diabetes, insulin resistance, diabetic neuropathy, diabetic nephropathy, diabetic retinopathy, cataracts, hyperglycemia, hypercholesterolemia, hypertension, hyperinsulinemia, hyperlipidemia, atherosclerosis, or tissue ischemia; and c) a container for containing the first and second compositions.
Also provided are methods of treating diabetes, insulin resistance, diabetic neuropathy, diabetic nephropathy, diabetic retinopathy, cataracts, hyperglycemia, hypercholesterolemia, hypertension, hyperinsulinemia, hyperlipidemia, atherosclerosis, or tissue ischemia, the method comprising the step of administering to a patient having diabetes, insulin resistance, diabetic neuropathy, diabetic nephropathy, diabetic retinopathy, cataracts, hyperglycemia, hypercholesterolemia, hypertension, hyperinsulinemia, hyperlipidemia, atherosclerosis, or tissue ischemia, a therapeutically effective amount of a compound of Formula I, stereoisomers, pharmaceutically acceptable salts and prodrugs thereof, and pharmaceutically acceptable salts of the prodrugs in combination with at least one additional compound useful for the treatment of diabetes, insulin resistance, diabetic neuropathy, diabetic nephropathy, diabetic retinopathy, cataracts, hyperglycemia, hypercholesterolemia, hypertension, hyperinsulinemia, hyperlipidemia, atherosclerosis, or tissue ischemia.
Also provided are pharmaceutical compositions comprising a compound of Formula I, stereoisomers, pharmaceutically acceptable salts and prodrugs thereof, and pharmaceutically acceptable salts of the prodrugs and at least one additional compound useful to treat diabetes, insulin resistance, diabetic neuropathy, diabetic nephropathy, diabetic retinopathy, cataracts, hyperglycemia, hypercholesterolemia, hypertension, hyperinsulinemia, hyperlipidemia, atherosclerosis, or tissue ischemia.

Problems solved by technology

In spite of the early discovery of insulin and its subsequent widespread use in the treatment of diabetes, and the later discovery of and use of sulfonylureas, biguanides and thiazolidinediones, such as troglitazone, rosiglitazone or pioglitazone, as oral hypoglycemic agents, the treatment of diabetes remains less than satisfactory.
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, or an agent may not be effective with a particular patient.
As a result, large segments of Western populations are now realized to be at particularly high risk.
While such “essential” hypertension is often associated with disorders such as obesity, diabetes and hypertriglyceridemia, the relationship between these disorders has not been elucidated.
It is known that hypertension can directly lead to heart failure, renal failure and stroke (brain hemorrhaging).
These conditions are capable of causing death in a patient.
These conditions gradually weaken a patient and can lead to death.
However, the development of atherosclerosis or heart disease due to hypertension over a long period of time remains a problem.
This implies that although high blood pressure is being reduced, the underlying cause of essential hypertension is not responding to this treatment.
These latter functions can be accomplished without affecting glucose levels and are known causes of hypertension.
Cardiac hypertrophy is a significant risk factor in the development of sudden death, myocardial infarction, and congestive heart failure.
Both non-cardiac and cardiac surgery are associated with substantial risks for myocardial infarction or death.
There is currently no marketed drug therapy in this area which reduces damage to cardiac tissue from perioperative myocardial ischemia or enhances cardiac resistance to ischemic episodes.
In addition to myocardial ischemia, other tissues can undergo ischemia and be damaged resulting in serious problems for the patient.
Likewise, in the postprandial (fed) state, where the liver has a proportionately smaller role in the total plasma glucose supply, hepatic glucose production is abnormally high in NIDDM patients.
Myocardial ischemic injury can occur in outpatient as well as in perioperative settings and can lead to the development of sudden death, myocardial infarction or congestive heart failure.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

preparation 1

Methyl 2,3-dihydroxy benzoate

A mixture of 92.472 g (0.6 mol) of 2,3-dihydroxybenzoic acid (FW 154.12; Aldrich cat.# 12,620-9; RSO # 9449), 100 mL of anhydrous methanol and 3 mL of concentrated sulfuric acid was heated to reflux for 36 hrs. After cooling down, reaction mixture was concentrated down to approximately ⅓ of its volume and poured on ice. A precipitate that formed was washed thoroughly with cold water, filtered off and dried in the desiccator over calcium sulfate. Yield 98.4 g of off-white solid (98%). This was used without further purification.

LC MS: AP+ 169, AP− 167.

preparation 2

3,4-Dihydro-2H-benzo[b][1,4]dioxepine-6-carboxylic acid methyl ester

A flame dried 1 L-flask was charged with 82.7 grams (0.6 mol) of finely ground and flame dried potassium carbonate and 200 mL of absolute dimethylformamide and kept under-nitrogen gas. This reaction mixture was then stirred and warmed up to 40° C. A 47.23 g (29.7 mL, 0.3 mol) of 1-bromo-3-chloropropane was then added to the reaction flask rapidly followed by 50.445 g (0.3 mol) of methyl 2,3-dihydroxy benzoate (C-2). The reaction was then heated to 100° C. (110° C. was the temp. of an oil bath) under reflux condenser for 6 hrs. After cooling, the reaction was filtered to remove all the solids, solids washed with 50 mL of, DMF and filtrate concentrated on the rotary evaporator. The residue was then partitioned between water and ethyl acetate. The organic layer was then washed with 200 mL of 1N NaOH to remove any starting material, followed by 5% HCl, 5% NaHCO3, water and brine. Dried with magnesium sulfate. Filtered...

preparation 3

8-Nitro-3,4-dihydro-2H-benzo[b][1,4]dioxepine-6-carboxylic acid methyl ester (C-4) and 9- Nitro-3,4-dihydro-2H-benzo[b][1,4]dioxepine-6-carboxylic acid methyl ester (C-5)

A 17.15 g (0.0825 mol) of (3,4-Dihydro-2H-benzo[b][1,4]dioxepine-6-carboxylic acid methyl ester; C-3) was dissolved in a mixture of 65 mL of glacial acetic acid and 65 mL of acetic anhydride. The reaction mixture was heated to 45° C. and treated with a solution of 12 mL of 90% HNO3 (fuming) inl2 mL of glacial acetic acid dropwise. The reaction was then heated to 45-50° C. for 4 hours under reflux condenser. When cooled down, the reaction mixture was poured on a mix of ice and water and the yellow precipitate collected on a filter. Washed with water and dried on air. Crude 17.6 grams (this product was a mixture of the meta- (about 30%). and paranitration (about 60%) products. This was used without further purification. LC MS: AP− 253 (for the mixture)

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Abstract

A compound of the formula wherein R1 is: R5 is: and n, m, Z, R8, R9, R10 and R11 are as defined herein, useful in the treatment of diabetes, insulin resistance, diabetic neuropathy, diabetic nephropathy, diabetic retinopathy, cataracts, hyperglycemia, hypercholesterolemia, hypertension, hyperinsulinemia, hyperlipidemia, atherosclerosis, and tissue ischemia, particularly, myocardial ischemia.

Description

BACKGROUND OF THE INVENTION The present invention relates to substituted 1H-(indole-2-carboxamides and 6H-thieno[2,3-b]pyrrole-5-carboxamides which are antidiabetic agents and as such are useful in the treatment of diabetes, insulin resistance, diabetic neuropathy, diabetic nephropathy, diabetic retinopathy, cataracts, hyperglycemia, hypercholesterolemia, hypertension, hyperinsulinemia, hyperlipidemia, atherosclerosis, and tissue ischemia, particularly myocardial ischemia. This invention also relates to a method of using such compounds in the treatment of the above diseases in mammals, especially humans, and to the pharmaceutical compositions useful therefor. In spite of the early discovery of insulin and its subsequent widespread use in the treatment of diabetes, and the later discovery of and use of sulfonylureas, biguanides and thiazolidinediones, such as troglitazone, rosiglitazone or pioglitazone, as oral hypoglycemic agents, the treatment of diabetes remains less than satis...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/357A61K31/404A61K31/407A61K31/5377A61K31/553A61P3/06A61P3/10A61P9/10A61P9/12A61P13/12A61P27/02A61P27/12A61P43/00C07D321/10C07D403/12C07D405/12C07D405/14C07D413/12C07D413/14C07D495/04
CPCC07D321/10C07D403/12C07D405/12C07D495/04C07D413/12C07D413/14C07D405/14A61P3/06A61P3/10A61P5/50A61P9/10A61P9/12A61P13/12A61P27/02A61P27/12A61P43/00
Inventor GAMMILL, RONALD B.
Owner GAMMILL RONALD B
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